Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 150350 |
|---|---|
| ensemblid | ENSG00000176177.10 |
| hgncid | 26352 |
| symbol | ENTHD1 |
| name | ENTH domain containing 1 |
| refseq_nuc | NM_152512.4 |
| refseq_prot | NP_689725.2 |
| ensembl_nuc | ENST00000325157.7 |
| ensembl_prot | ENSP00000317431.6 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 39743044 |
| end | 39893760 |
| strand | - |
| ver | v1.2 |
| region | chr22:39743044-39893760 |
| region5000 | chr22:39738044-39898760 |
| regionname0 | ENTHD1_chr22_39743044_39893760 |
| regionname5000 | ENTHD1_chr22_39738044_39898760 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 607 | 206 | 55 | 41 | 81 | 6 | 21 | 63 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0002 | 0/0 | 607 | 8 | 0 | 7 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0003 | 0/0 | 607 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0004 | 0/0 | 607 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0005 | 0/0 | 607 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0006 | 0/0 | 607 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1824 | 200 | 50 | 41 | 80 | 6 | 21 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| c0002 | 0/0 | 1824 | 8 | 0 | 7 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| c0003 | 0/0 | 1824 | 3 | 3 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| c0004 | 0/0 | 1824 | 2 | 2 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| c0005 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| c0006 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| c0007 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| c0008 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| c0009 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 857 | 185 | 54 | 37 | 71 | 5 | 17 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| t0002 | 0/0 | 857 | 27 | 0 | 11 | 11 | 1 | 4 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| t0003 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| t0004 | 0/0 | 857 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| t0005 | 0/1 | 857 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| t0006 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| t0007 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| t0008 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1824 | 200 | 50 | 41 | 80 | 6 | 21 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0003 | 0/0 | 1824 | 3 | 3 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0004 | 0/0 | 1824 | 2 | 2 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0008 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0002c0002 | 0/0 | 1824 | 8 | 0 | 7 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0003c0006 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0004c0009 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0005c0007 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0006c0005 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2680 | 167 | 46 | 30 | 69 | 5 | 16 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0001t0002 | 0/0 | 2680 | 27 | 0 | 11 | 11 | 1 | 4 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0001t0003 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0001t0004 | 0/0 | 2680 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0001t0005 | 0/1 | 2680 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0001t0006 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0001t0007 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0001t0008 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0003t0001 | 0/0 | 2680 | 3 | 3 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0004t0001 | 0/0 | 2680 | 2 | 2 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0001c0008t0001 | 0/0 | 2680 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0002c0002t0001 | 0/0 | 2680 | 8 | 0 | 7 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0003c0006t0001 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0004c0009t0001 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0005c0007t0001 | 0/0 | 2680 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| a0006c0005t0001 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | copy fasta | chr22 | 39738044 | 39898760 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0005g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0003t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0008t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0003c0006t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0004c0009t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0005c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0006c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0203 | EUR | FIN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01891 | hp1 | a0006 | c0005 | t0001 | g0019 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0094 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0093 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02717 | hp1 | a0003 | c0006 | t0001 | g0196 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02922 | hp1 | a0004 | c0009 | t0001 | g0153 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | BEB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0174 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18983 | hp2 | a0001 | c0008 | t0001 | g0140 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19000 | hp1 | a0005 | c0007 | t0001 | g0125 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | GIH | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | GIH | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0113 | REF | REF | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0058 | REF | REF | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39743860
|
A | G | 1 | a0004 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1643T>C | p.Ile548Thr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 1864/2680 | 1643/1824 | 548/607 | chr22 | 39743860 | ||
| chr22:39744176
|
C | T | 1 | a0005 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.1327G>A | p.Gly443Arg | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 1548/2680 | 1327/1824 | 443/607 | chr22 | 39744176 | ||
| chr22:39765300
|
A | G | 1 | a0003 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1142T>C | p.Val381Ala | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/7 | 1363/2680 | 1142/1824 | 381/607 | chr22 | 39765300 | ||
| chr22:39765434
|
C | G | 1 | a0006 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1008G>C | p.Trp336Cys | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/7 | 1229/2680 | 1008/1824 | 336/607 | chr22 | 39765434 | ||
| chr22:39765567
|
C | G | 1 | a0006 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.875G>C | p.Arg292Thr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/7 | 1096/2680 | 875/1824 | 292/607 | chr22 | 39765567 | ||
| chr22:39861778
|
C | G | 1 | a0006 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.579G>C | p.Arg193Ser | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/7 | 800/2680 | 579/1824 | 193/607 | chr22 | 39861778 | ||
| chr22:39887423
|
A | G | 1 | a0002 | 8 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(5): Show |
missense_variant | MODERATE | c.326T>C | p.Ile109Thr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/7 | 547/2680 | 326/1824 | 109/607 | chr22 | 39887423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39744132
|
G | T | 1 | a0001c0008 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.1371C>A | p.Thr457Thr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 1592/2680 | 1371/1824 | 457/607 | chr22 | 39744132 | ||
| chr22:39744158
|
G | A | 1 | a0006c0005 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1345C>T | p.Leu449Leu | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 1566/2680 | 1345/1824 | 449/607 | chr22 | 39744158 | ||
| chr22:39862000
|
A | G | 1 | a0001c0004 | 2 | HG02258.hp1 HG02572.hp2 |
synonymous_variant | LOW | c.357T>C | p.Tyr119Tyr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/7 | 578/2680 | 357/1824 | 119/607 | chr22 | 39862000 | ||
| chr22:39887557
|
A | G | 1 | a0001c0003 | 3 | HG02622.hp2 HG02723.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.192T>C | p.His64His | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/7 | 413/2680 | 192/1824 | 64/607 | chr22 | 39887557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39743145
|
T | C | 1 | a0001c0001t0007 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*534A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 534 | chr22 | 39743145 | |||||
| chr22:39743243
|
G | A | 1 | a0001c0001t0008 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 436 | chr22 | 39743243 | |||||
| chr22:39743251
|
C | G | 1 | a0001c0001t0006 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*428G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 428 | chr22 | 39743251 | |||||
| chr22:39743394
|
A | G | 1 | a0001c0001t0005 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*285T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 285 | chr22 | 39743394 | |||||
| chr22:39743434
|
A | G | 2 | a0001c0001t0002a0001c0001t0004 | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*245T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 245 | chr22 | 39743434 | |||||
| chr22:39893708
|
C | T | 1 | a0001c0001t0004 | 1 | HG03927.hp1 | 5_prime_UTR_variant | MODIFIER | c.-169G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/7 | 5960 | chr22 | 39893708 | |||||
| chr22:39893722
|
C | T | 1 | a0001c0001t0003 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-183G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/7 | 5974 | chr22 | 39893722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39744294
|
T | C | 1 | a0002c0002t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1220-11A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744294 | ||||||
| chr22:39744439
|
A | C | 30 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(27): Show | 30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1220-156T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744439 | ||||||
| chr22:39744469
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0029others(1): Show | 4 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220-186G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744469 | ||||||
| chr22:39744527
|
TTCATCTT others(3): Show |
T | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1220-254_1220-245d others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744527 | ||||||
| chr22:39744734
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1220-451G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744734 | ||||||
| chr22:39744963
|
T | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-680A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744963 | ||||||
| chr22:39745045
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1220-762A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745045 | ||||||
| chr22:39745284
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0006g0214 | 2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1220-1001G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745284 | ||||||
| chr22:39745539
|
T | G | 3 | a0001c0001t0001g0023a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1220-1256A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745539 | ||||||
| chr22:39745658
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1220-1375G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745658 | ||||||
| chr22:39745768
|
G | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0097a0001c0001t0001g0105others(2): Show | 5 | HG00438.hp2 NA18984.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220-1485C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745768 | ||||||
| chr22:39745794
|
G | A | 27 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1220-1511C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745794 | ||||||
| chr22:39745894
|
G | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1220-1611C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745894 | ||||||
| chr22:39745917
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-1634G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745917 | ||||||
| chr22:39746210
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-1927T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746210 | ||||||
| chr22:39746244
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1220-1961T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746244 | ||||||
| chr22:39746526
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-2243G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746526 | ||||||
| chr22:39746567
|
G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1220-2284C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746567 | ||||||
| chr22:39746901
|
T | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-2618A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746901 | ||||||
| chr22:39747286
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0141 | 2 | NA18988.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1220-3003G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747286 | ||||||
| chr22:39747324
|
A | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0036others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220-3041T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747324 | ||||||
| chr22:39747346
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1220-3063C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747346 | ||||||
| chr22:39747572
|
A | G | 27 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1220-3289T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747572 | ||||||
| chr22:39747977
|
G | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(17): Show | 21 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1220-3694C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747977 | ||||||
| chr22:39748024
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1220-3741C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748024 | ||||||
| chr22:39748030
|
C | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1220-3747G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748030 | ||||||
| chr22:39748041
|
G | A | 1 | a0004c0009t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1220-3758C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748041 | ||||||
| chr22:39748047
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1220-3764C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748047 | ||||||
| chr22:39748249
|
C | CA | 11 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0088others(8): Show | 11 | HG00738.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1220-3967dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748249 | ||||||
| chr22:39748379
|
C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-4096G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748379 | ||||||
| chr22:39748385
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1220-4102G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748385 | ||||||
| chr22:39748386
|
G | A | 1 | a0004c0009t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1220-4103C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748386 | ||||||
| chr22:39748427
|
CT | C | 38 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1220-4145delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748427 | ||||||
| chr22:39748432
|
T | C | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 4 | HG00140.hp1 HG01070.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1220-4149A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748432 | ||||||
| chr22:39748507
|
T | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-4224A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748507 | ||||||
| chr22:39748512
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0097a0001c0001t0001g0105others(2): Show | 5 | HG00438.hp2 NA18984.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220-4229G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748512 | ||||||
| chr22:39748557
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1220-4274T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748557 | ||||||
| chr22:39748569
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1220-4286G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748569 | ||||||
| chr22:39748586
|
AT | A | 38 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1220-4304delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748586 | ||||||
| chr22:39748595
|
T | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0056others(1): Show | 4 | HG02135.hp2 NA18979.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1220-4312A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748595 | ||||||
| chr22:39748599
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-4316C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748599 | ||||||
| chr22:39748669
|
T | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-4386A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748669 | ||||||
| chr22:39749031
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1220-4748G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749031 | ||||||
| chr22:39749354
|
T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-5071A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749354 | ||||||
| chr22:39749454
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-5171C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749454 | ||||||
| chr22:39749612
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1220-5329A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749612 | ||||||
| chr22:39749698
|
T | C | 33 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0002g0154others(30): Show | 33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1220-5415A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749698 | ||||||
| chr22:39749836
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1220-5553T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749836 | ||||||
| chr22:39749857
|
G | A | 2 | a0001c0001t0001g0023a0001c0004t0001g0094 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1220-5574C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749857 | ||||||
| chr22:39749989
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0121 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1220-5706G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749989 | ||||||
| chr22:39750280
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0130 | 2 | NA18968.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1220-5997C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39750280 | ||||||
| chr22:39750526
|
G | T | 2 | a0001c0001t0001g0023a0001c0004t0001g0094 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1220-6243C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39750526 | ||||||
| chr22:39750743
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-6460T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39750743 | ||||||
| chr22:39750754
|
T | A | 2 | a0001c0001t0001g0023a0001c0004t0001g0094 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1220-6471A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39750754 | ||||||
| chr22:39751146
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-6863C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39751146 | ||||||
| chr22:39751505
|
T | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0197 | 3 | HG02630.hp1 HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1220-7222A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39751505 | ||||||
| chr22:39751759
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1220-7476A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39751759 | ||||||
| chr22:39751985
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0003g0004 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1220-7702C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39751985 | ||||||
| chr22:39752114
|
G | GATATACT others(19): Show |
1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1220-7857_1220-783 others(30): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39752114 | ||||||
| chr22:39752114
|
G | T | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1220-7831C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39752114 | ||||||
| chr22:39753022
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1220-8739C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753022 | ||||||
| chr22:39753037
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-8754T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753037 | ||||||
| chr22:39753213
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1220-8930A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753213 | ||||||
| chr22:39753389
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1220-9106T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753389 | ||||||
| chr22:39753696
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0189 | 3 | HG01884.hp2 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1220-9413C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753696 | ||||||
| chr22:39753725
|
T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1220-9442A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753725 | ||||||
| chr22:39753739
|
C | T | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1220-9456G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753739 | ||||||
| chr22:39753913
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-9630C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753913 | ||||||
| chr22:39754048
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-9765G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754048 | ||||||
| chr22:39754066
|
G | A | 2 | a0001c0001t0006g0214a0006c0005t0001g0019 | 2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1220-9783C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754066 | ||||||
| chr22:39754280
|
T | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0101others(1): Show | 4 | HG00597.hp1 HG00673.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220-9997A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754280 | ||||||
| chr22:39754281
|
A | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-9998T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754281 | ||||||
| chr22:39754741
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-10458G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754741 | ||||||
| chr22:39754977
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1219+10246G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754977 | ||||||
| chr22:39755172
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+10051G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755172 | ||||||
| chr22:39755229
|
T | C | 2 | a0001c0001t0001g0023a0001c0004t0001g0094 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1219+9994A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755229 | ||||||
| chr22:39755338
|
G | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+9885C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755338 | ||||||
| chr22:39755438
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219+9785G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755438 | ||||||
| chr22:39755515
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1219+9708G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755515 | ||||||
| chr22:39755560
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219+9663C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755560 | ||||||
| chr22:39755874
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1219+9349T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755874 | ||||||
| chr22:39756281
|
G | GTC | 2 | a0001c0001t0001g0116a0001c0001t0001g0189 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1219+8940_1219+894 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756281 | ||||||
| chr22:39756287
|
G | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0189 | 3 | HG01884.hp2 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1219+8936C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | ||||||
| chr22:39756287
|
G | GTC | 36 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(33): Show | 36 | HG00735.hp1 HG01257.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.1219+8934_1219+893 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | ||||||
| chr22:39756287
|
G | GTCTC | 11 | a0001c0001t0001g0048a0001c0001t0001g0129a0001c0001t0001g0131others(8): Show | 11 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1219+8932_1219+893 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | ||||||
| chr22:39756287
|
GTC | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0030others(31): Show | 35 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1219+8934_1219+893 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | ||||||
| chr22:39756287
|
GTCTCTC | G | 2 | a0001c0001t0001g0177a0001c0001t0002g0154 | 2 | NA18522.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1219+8930_1219+893 others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | ||||||
| chr22:39756308
|
TCTCTCTC others(3): Show |
T | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1219+8905_1219+891 others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756308 | ||||||
| chr22:39756314
|
T | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0080 | 2 | HG00621.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1219+8909A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756314 | ||||||
| chr22:39756314
|
T | TCA | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(2): Show | 5 | HG02083.hp1 NA18944.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219+8908_1219+890 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756314 | ||||||
| chr22:39756316
|
T | A | 71 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0030others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1219+8907A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756316 | ||||||
| chr22:39756316
|
T | TCA | 33 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(30): Show | 35 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1219+8905_1219+890 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756316 | ||||||
| chr22:39756316
|
T | TCTCTCTC others(19): Show |
1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+8906_1219+890 others(30): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756316 | ||||||
| chr22:39756318
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1219+8905T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756318 | ||||||
| chr22:39756327
|
C | G | 27 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1219+8896G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756327 | ||||||
| chr22:39756340
|
G | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219+8883C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756340 | ||||||
| chr22:39756342
|
A | ACG | 2 | a0001c0001t0001g0092a0001c0001t0001g0115 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1219+8880_1219+888 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756342 | ||||||
| chr22:39756342
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0189a0001c0001t0006g0214 | 3 | HG01884.hp2 HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1219+8881T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756342 | ||||||
| chr22:39756622
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+8601T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756622 | ||||||
| chr22:39756628
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+8595G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756628 | ||||||
| chr22:39756659
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1219+8564T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756659 | ||||||
| chr22:39757014
|
C | CA | 8 | a0001c0001t0001g0043a0001c0001t0001g0181a0001c0001t0001g0186others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219+8208dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757014 | ||||||
| chr22:39757014
|
CA | C | 34 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0173others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.1219+8208delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757014 | ||||||
| chr22:39757311
|
T | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+7912A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757311 | ||||||
| chr22:39757441
|
T | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+7782A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757441 | ||||||
| chr22:39757508
|
C | G | 1 | a0001c0001t0002g0166 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1219+7715G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757508 | ||||||
| chr22:39757520
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1219+7703A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757520 | ||||||
| chr22:39757576
|
C | CTGAGGCA others(11): Show |
1 | a0001c0001t0001g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1219+7629_1219+764 others(22): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757576 | ||||||
| chr22:39757690
|
T | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02886.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1219+7533A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757690 | ||||||
| chr22:39757783
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1219+7440G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757783 | ||||||
| chr22:39758031
|
A | G | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1219+7192T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758031 | ||||||
| chr22:39758038
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1219+7185G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758038 | ||||||
| chr22:39758205
|
T | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1219+7018A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758205 | ||||||
| chr22:39758450
|
T | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+6773A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758450 | ||||||
| chr22:39758583
|
C | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+6640G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758583 | ||||||
| chr22:39758811
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+6412T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758811 | ||||||
| chr22:39758871
|
A | T | 22 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0054others(19): Show | 22 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1219+6352T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758871 | ||||||
| chr22:39758947
|
G | A | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1219+6276C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758947 | ||||||
| chr22:39759172
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1219+6051C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759172 | ||||||
| chr22:39759281
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0130 | 2 | NA18968.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1219+5942T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759281 | ||||||
| chr22:39759551
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1219+5672G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759551 | ||||||
| chr22:39759632
|
T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(13): Show | 17 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1219+5591A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759632 | ||||||
| chr22:39759693
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1219+5530G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759693 | ||||||
| chr22:39759926
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1219+5297C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759926 | ||||||
| chr22:39759928
|
G | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+5295C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759928 | ||||||
| chr22:39760076
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1219+5147C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39760076 | ||||||
| chr22:39760203
|
A | C | 1 | a0001c0001t0001g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1219+5020T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39760203 | ||||||
| chr22:39760268
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1219+4955G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39760268 | ||||||
| chr22:39760980
|
C | T | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1219+4243G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39760980 | ||||||
| chr22:39761111
|
T | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+4112A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761111 | ||||||
| chr22:39761246
|
A | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(84): Show | 89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1219+3977T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761246 | ||||||
| chr22:39761249
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1219+3974C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761249 | ||||||
| chr22:39761499
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+3724C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761499 | ||||||
| chr22:39761580
|
GAC | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1219+3641_1219+364 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761580 | ||||||
| chr22:39762196
|
C | T | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0005c0007t0001g0125 | 3 | NA18977.hp1 NA19000.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1219+3027G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762196 | ||||||
| chr22:39762212
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1219+3011G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762212 | ||||||
| chr22:39762223
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1219+3000A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762223 | ||||||
| chr22:39762438
|
ATCTCACT others(13): Show |
A | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1219+2765_1219+278 others(24): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762438 | ||||||
| chr22:39762526
|
C | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+2697G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762526 | ||||||
| chr22:39762622
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+2601C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762622 | ||||||
| chr22:39762928
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1219+2295A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762928 | ||||||
| chr22:39763248
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1219+1975A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39763248 | ||||||
| chr22:39763407
|
T | C | 1 | a0001c0003t0001g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1219+1816A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39763407 | ||||||
| chr22:39763438
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1219+1785G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39763438 | ||||||
| chr22:39764094
|
T | C | 1 | a0002c0002t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1219+1129A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764094 | ||||||
| chr22:39764198
|
A | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0006g0214others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219+1025T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764198 | ||||||
| chr22:39764299
|
C | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+924G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764299 | ||||||
| chr22:39764503
|
A | G | 9 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0077others(6): Show | 9 | HG00738.hp2 HG01106.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219+720T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764503 | ||||||
| chr22:39764524
|
TATGTAAG others(40): Show |
T | 1 | a0001c0001t0001g0124 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1219+652_1219+698d others(49): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764524 | ||||||
| chr22:39764542
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1219+681T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764542 | ||||||
| chr22:39764786
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1219+437T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764786 | ||||||
| chr22:39764860
|
A | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+363T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764860 | ||||||
| chr22:39764861
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+362G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764861 | ||||||
| chr22:39764935
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+288T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764935 | ||||||
| chr22:39764976
|
T | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+247A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764976 | ||||||
| chr22:39765176
|
T | TTG | 23 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0061others(20): Show | 23 | HG00642.hp2 HG00673.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1219+45_1219+46dup others(2): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | ||||||
| chr22:39765176
|
T | TTGTGTG | 3 | a0001c0001t0001g0152a0001c0001t0001g0201a0001c0001t0008g0015 | 3 | HG00639.hp2 HG02559.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1219+41_1219+46dup others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | ||||||
| chr22:39765176
|
T | TTGTGTGT others(1): Show |
24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1219+39_1219+46dup others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | ||||||
| chr22:39765176
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1219+37_1219+46dup others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | ||||||
| chr22:39765176
|
TTG | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0044others(26): Show | 29 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1219+45_1219+46del others(2): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | ||||||
| chr22:39765176
|
TTGTG | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0186 | 2 | HG02258.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1219+43_1219+46del others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | ||||||
| chr22:39765678
|
T | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.833-69A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39765678 | ||||||
| chr22:39765826
|
C | G | 3 | a0001c0001t0001g0198a0001c0003t0001g0006a0003c0006t0001g0196 | 3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.833-217G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39765826 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0205 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.833-420_833-411dup others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(4): Show |
8 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG00323.hp1 HG01070.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.833-421_833-411dup others(11): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(5): Show |
7 | a0001c0001t0002g0154a0001c0001t0002g0156a0001c0001t0002g0158others(4): Show | 7 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.833-422_833-411dup others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0204 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.833-423_833-411dup others(13): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0002g0157a0001c0001t0002g0208 | 2 | HG00642.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.833-424_833-411dup others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0004g0005 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.833-425_833-411dup others(15): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.833-426_833-411dup others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0002g0163a0001c0001t0002g0171 | 2 | NA19002.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.833-427_833-411dup others(17): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0002g0155a0001c0001t0002g0167a0001c0001t0002g0172 | 3 | NA19010.hp2 NA19077.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.833-428_833-411dup others(18): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0002g0162 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.833-429_833-411dup others(19): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0002g0169 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.833-430_833-411dup others(20): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
CA | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.833-411delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
CAA | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00673.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.833-412_833-411del others(2): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0170 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.833-422_833-411del others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
CAAAAAAA others(6): Show |
C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-423_833-411del others(13): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766019
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0177a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02886.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.833-424_833-411del others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | ||||||
| chr22:39766107
|
T | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-498A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766107 | ||||||
| chr22:39766593
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.833-984G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766593 | ||||||
| chr22:39766594
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-985C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766594 | ||||||
| chr22:39766613
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-1004C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766613 | ||||||
| chr22:39766642
|
A | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.833-1033T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766642 | ||||||
| chr22:39766656
|
T | A | 1 | a0001c0001t0002g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.833-1047A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766656 | ||||||
| chr22:39766802
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0184 | 2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.833-1193T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766802 | ||||||
| chr22:39767042
|
T | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0121 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.833-1433A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767042 | ||||||
| chr22:39767462
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.833-1853T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767462 | ||||||
| chr22:39767462
|
AAAAACAA others(3): Show |
A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-1863_833-1854d others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767462 | ||||||
| chr22:39767492
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-1883T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767492 | ||||||
| chr22:39767617
|
T | C | 3 | a0001c0001t0001g0014a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-2008A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767617 | ||||||
| chr22:39767630
|
T | C | 1 | a0004c0009t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.833-2021A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767630 | ||||||
| chr22:39767752
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.833-2143T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767752 | ||||||
| chr22:39767888
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.833-2279G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767888 | ||||||
| chr22:39768155
|
C | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(14): Show | 18 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.833-2546G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768155 | ||||||
| chr22:39768286
|
G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-2677C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768286 | ||||||
| chr22:39768434
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.833-2825T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768434 | ||||||
| chr22:39768441
|
A | C | 3 | a0001c0001t0001g0014a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-2832T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768441 | ||||||
| chr22:39768623
|
C | T | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.833-3014G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768623 | ||||||
| chr22:39768682
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.833-3073T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768682 | ||||||
| chr22:39768867
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.833-3258C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768867 | ||||||
| chr22:39768946
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-3337T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768946 | ||||||
| chr22:39768987
|
C | CACACACT others(23): Show |
1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833-3408_833-3379d others(32): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768987 | ||||||
| chr22:39768987
|
CACACACT others(23): Show |
C | 1 | a0001c0001t0001g0091 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.833-3408_833-3379d others(32): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768987 | ||||||
| chr22:39769079
|
T | TACACACA others(57): Show |
1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-3471_833-3470i others(66): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769079 | ||||||
| chr22:39769088
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-3479T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769088 | ||||||
| chr22:39769154
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(82): Show | 87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.833-3545C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769154 | ||||||
| chr22:39769227
|
T | C | 7 | a0001c0001t0002g0155a0001c0001t0002g0162a0001c0001t0002g0163others(4): Show | 7 | NA18988.hp2 NA18998.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.833-3618A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769227 | ||||||
| chr22:39769331
|
G | A | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-3722C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769331 | ||||||
| chr22:39769568
|
G | C | 30 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(27): Show | 30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.833-3959C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769568 | ||||||
| chr22:39769569
|
G | A | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-3960C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769569 | ||||||
| chr22:39769659
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.833-4050T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769659 | ||||||
| chr22:39769687
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 215 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.833-4078T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769687 | ||||||
| chr22:39769850
|
T | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(16): Show | 20 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.833-4241A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769850 | ||||||
| chr22:39769934
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.833-4325G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769934 | ||||||
| chr22:39769941
|
G | GATTGTGA others(18): Show |
1 | a0001c0001t0001g0124 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.833-4333_833-4332i others(27): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769941 | ||||||
| chr22:39769942
|
T | G | 1 | a0001c0001t0001g0124 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.833-4333A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769942 | ||||||
| chr22:39770352
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.833-4743G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770352 | ||||||
| chr22:39770462
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-4853G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770462 | ||||||
| chr22:39770469
|
A | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-4860T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770469 | ||||||
| chr22:39770605
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 158 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.833-4996C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770605 | ||||||
| chr22:39770652
|
T | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-5043A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770652 | ||||||
| chr22:39770762
|
A | ACTTGGAT others(29): Show |
1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.833-5189_833-5154d others(38): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770762 | ||||||
| chr22:39770982
|
T | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-5373A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770982 | ||||||
| chr22:39771077
|
G | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(66): Show | 70 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.833-5468C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771077 | ||||||
| chr22:39771085
|
C | CT | 4 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 5 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-5477dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771085 | ||||||
| chr22:39771125
|
TG | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0060 | 2 | NA18942.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.833-5517delC | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771125 | ||||||
| chr22:39771138
|
G | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.833-5529C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771138 | ||||||
| chr22:39771185
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-5576C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771185 | ||||||
| chr22:39771988
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.833-6379G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771988 | ||||||
| chr22:39772433
|
G | T | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.833-6824C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39772433 | ||||||
| chr22:39772605
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.833-6996T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39772605 | ||||||
| chr22:39773117
|
C | CA | 18 | a0001c0001t0001g0014a0001c0001t0001g0048a0001c0001t0001g0062others(15): Show | 18 | HG00621.hp2 HG01081.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.833-7509dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | ||||||
| chr22:39773117
|
C | CAAAAAAA others(5): Show |
1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-7520_833-7509d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | ||||||
| chr22:39773117
|
CA | C | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(61): Show | 66 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.833-7509delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | ||||||
| chr22:39773117
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0038 | 3 | HG02055.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.833-7520_833-7509d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | ||||||
| chr22:39773117
|
CAAAAAAA others(6): Show |
C | 20 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(17): Show | 21 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.833-7521_833-7509d others(15): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | ||||||
| chr22:39773921
|
T | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(84): Show | 89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.833-8312A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773921 | ||||||
| chr22:39773959
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-8350C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773959 | ||||||
| chr22:39774067
|
C | T | 9 | a0001c0001t0001g0050a0001c0001t0001g0071a0001c0001t0001g0077others(6): Show | 9 | HG00738.hp2 HG01106.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.833-8458G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774067 | ||||||
| chr22:39774413
|
T | C | 3 | a0001c0001t0001g0198a0001c0003t0001g0006a0003c0006t0001g0196 | 3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.833-8804A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774413 | ||||||
| chr22:39774462
|
A | C | 1 | a0001c0001t0001g0089 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.833-8853T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774462 | ||||||
| chr22:39774578
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.833-8969G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774578 | ||||||
| chr22:39774629
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.833-9020A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774629 | ||||||
| chr22:39774772
|
C | T | 1 | a0001c0001t0002g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.833-9163G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774772 | ||||||
| chr22:39774885
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.833-9276G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774885 | ||||||
| chr22:39775245
|
T | G | 1 | a0001c0003t0001g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.833-9636A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775245 | ||||||
| chr22:39775269
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.833-9660G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775269 | ||||||
| chr22:39775383
|
A | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0131 | 2 | NA18947.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.833-9774T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775383 | ||||||
| chr22:39775706
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.833-10097G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775706 | ||||||
| chr22:39775828
|
T | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0146others(2): Show | 5 | HG02735.hp1 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-10219A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775828 | ||||||
| chr22:39776037
|
GC | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0081others(1): Show | 4 | HG02258.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.833-10429delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776037 | ||||||
| chr22:39776083
|
G | A | 3 | a0001c0001t0001g0014a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-10474C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776083 | ||||||
| chr22:39776130
|
T | G | 2 | a0001c0001t0001g0188a0001c0001t0003g0004 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.833-10521A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776130 | ||||||
| chr22:39776193
|
A | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-10584T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776193 | ||||||
| chr22:39776712
|
A | C | 3 | a0001c0001t0001g0014a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-11103T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776712 | ||||||
| chr22:39777267
|
T | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.833-11658A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777267 | ||||||
| chr22:39777555
|
A | C | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.833-11946T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777555 | ||||||
| chr22:39777893
|
C | T | 3 | a0001c0001t0001g0014a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-12284G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777893 | ||||||
| chr22:39777915
|
G | T | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.833-12306C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777915 | ||||||
| chr22:39777916
|
C | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-12307G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777916 | ||||||
| chr22:39778165
|
G | C | 4 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0001g0109others(1): Show | 4 | HG00621.hp2 HG02027.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.833-12556C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778165 | ||||||
| chr22:39778367
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0184 | 2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.833-12758T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778367 | ||||||
| chr22:39778457
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-12848G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778457 | ||||||
| chr22:39778599
|
T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-12990A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778599 | ||||||
| chr22:39778680
|
A | G | 3 | a0001c0001t0001g0014a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-13071T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778680 | ||||||
| chr22:39778865
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-13256A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778865 | ||||||
| chr22:39778887
|
A | C | 2 | a0001c0001t0001g0188a0001c0001t0003g0004 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.833-13278T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778887 | ||||||
| chr22:39778890
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-13281G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778890 | ||||||
| chr22:39779249
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.833-13640T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779249 | ||||||
| chr22:39779336
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.833-13727C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779336 | ||||||
| chr22:39779402
|
C | T | 4 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0208others(1): Show | 4 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-13793G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779402 | ||||||
| chr22:39779434
|
A | G | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.833-13825T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779434 | ||||||
| chr22:39779556
|
GA | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(22): Show | 26 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.833-13948delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779556 | ||||||
| chr22:39780098
|
G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-14489C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780098 | ||||||
| chr22:39780140
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.833-14531T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780140 | ||||||
| chr22:39780166
|
G | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-14557C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780166 | ||||||
| chr22:39780240
|
C | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(16): Show | 20 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.833-14631G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780240 | ||||||
| chr22:39780249
|
C | T | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-14640G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780249 | ||||||
| chr22:39780280
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.833-14671C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780280 | ||||||
| chr22:39780312
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.833-14703C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780312 | ||||||
| chr22:39780375
|
C | CA | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0055others(12): Show | 15 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.833-14767dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780375 | ||||||
| chr22:39780375
|
C | CAA | 38 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0049others(35): Show | 38 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.833-14768_833-1476 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780375 | ||||||
| chr22:39780375
|
CA | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0026others(20): Show | 23 | HG00639.hp2 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.833-14767delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780375 | ||||||
| chr22:39780568
|
A | G | 19 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 20 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.833-14959T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780568 | ||||||
| chr22:39780569
|
GTTATAC | G | 2 | a0001c0001t0001g0188a0001c0001t0003g0004 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.833-14966_833-1496 others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780569 | ||||||
| chr22:39780644
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.833-15035A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780644 | ||||||
| chr22:39780766
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.833-15157C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780766 | ||||||
| chr22:39780799
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.833-15190G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780799 | ||||||
| chr22:39780870
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-15261C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780870 | ||||||
| chr22:39780998
|
C | CA | 27 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.833-15390dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780998 | ||||||
| chr22:39780998
|
C | CAAAAAAA others(3): Show |
20 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(17): Show | 21 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.833-15399_833-1539 others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780998 | ||||||
| chr22:39780998
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0034 | 2 | HG02257.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.833-15400_833-1539 others(15): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780998 | ||||||
| chr22:39781225
|
A | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.833-15616T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39781225 | ||||||
| chr22:39781280
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.833-15671A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39781280 | ||||||
| chr22:39781987
|
A | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-16378T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39781987 | ||||||
| chr22:39781991
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.833-16382A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39781991 | ||||||
| chr22:39782032
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.833-16423T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782032 | ||||||
| chr22:39782038
|
G | T | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-16429C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782038 | ||||||
| chr22:39782060
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-16451C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782060 | ||||||
| chr22:39782220
|
A | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-16611T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782220 | ||||||
| chr22:39782231
|
G | T | 10 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0051others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.833-16622C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782231 | ||||||
| chr22:39782614
|
T | C | 3 | a0001c0001t0001g0198a0001c0003t0001g0006a0003c0006t0001g0196 | 3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.833-17005A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782614 | ||||||
| chr22:39782629
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-17020T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782629 | ||||||
| chr22:39782983
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(67): Show | 71 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.833-17374C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782983 | ||||||
| chr22:39783521
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.833-17912G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39783521 | ||||||
| chr22:39783635
|
G | GA | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-18027dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39783635 | ||||||
| chr22:39783823
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0003g0004 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.833-18214T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39783823 | ||||||
| chr22:39784325
|
G | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0144 | 2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.833-18716C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784325 | ||||||
| chr22:39784543
|
T | TAC | 18 | a0001c0001t0001g0120a0001c0001t0001g0143a0001c0001t0001g0173others(15): Show | 18 | HG01496.hp2 HG02145.hp1 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.833-18936_833-1893 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
T | TACAC | 9 | a0001c0001t0001g0020a0001c0001t0001g0092a0001c0001t0001g0188others(6): Show | 9 | HG01070.hp2 HG01192.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.833-18938_833-1893 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
T | TACACAC | 9 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0081others(6): Show | 9 | HG00323.hp1 HG00642.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.833-18940_833-1893 others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
T | TACACACA others(1): Show |
6 | a0001c0001t0002g0155a0001c0001t0002g0161a0001c0001t0002g0162others(3): Show | 6 | NA18998.hp2 NA19010.hp2 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-18942_833-1893 others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
T | TACACACA others(3): Show |
4 | a0001c0001t0001g0082a0001c0001t0002g0154a0001c0001t0002g0164others(1): Show | 4 | HG02258.hp2 NA18988.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.833-18944_833-1893 others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
T | TACACACA others(5): Show |
2 | a0001c0001t0002g0157a0001c0001t0002g0163 | 2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.833-18946_833-1893 others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
T | TACACACA others(7): Show |
5 | a0001c0001t0001g0014a0001c0001t0002g0156a0001c0001t0002g0160others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-18948_833-1893 others(18): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
T | TACACACA others(9): Show |
3 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0165 | 3 | HG01081.hp2 HG01257.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.833-18950_833-1893 others(20): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
T | TACACACA others(11): Show |
1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-18952_833-1893 others(22): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
T | TACACACA others(15): Show |
1 | a0001c0001t0002g0166 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.833-18956_833-1893 others(26): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
TAC | T | 66 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(63): Show | 67 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.833-18936_833-1893 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
TACAC | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0051a0001c0001t0001g0065others(9): Show | 12 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.833-18938_833-1893 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784543
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.833-18946_833-1893 others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | ||||||
| chr22:39784582
|
A | ACT | 13 | a0001c0001t0001g0018a0001c0001t0001g0026a0001c0001t0001g0027others(10): Show | 13 | HG01496.hp1 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.833-18975_833-1897 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784582 | ||||||
| chr22:39784582
|
A | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0024others(7): Show | 11 | HG00323.hp2 HG01069.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.833-18973T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784582 | ||||||
| chr22:39784586
|
G | A | 30 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(27): Show | 30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.833-18977C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784586 | ||||||
| chr22:39784812
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.833-19203C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784812 | ||||||
| chr22:39784880
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.833-19271A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784880 | ||||||
| chr22:39785132
|
A | AAGAT | 62 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(59): Show | 63 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.833-19527_833-1952 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785132 | ||||||
| chr22:39785155
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.833-19546T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785155 | ||||||
| chr22:39785169
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.833-19560G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785169 | ||||||
| chr22:39785193
|
G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-19584C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785193 | ||||||
| chr22:39785311
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.833-19702C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785311 | ||||||
| chr22:39785327
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.833-19718C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785327 | ||||||
| chr22:39785583
|
T | C | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-19974A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785583 | ||||||
| chr22:39785827
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.833-20218T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785827 | ||||||
| chr22:39786268
|
T | G | 3 | a0001c0001t0002g0156a0001c0001t0002g0158a0001c0001t0002g0160 | 3 | HG01081.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.833-20659A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786268 | ||||||
| chr22:39786424
|
AT | A | 5 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158others(2): Show | 5 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-20816delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786424 | ||||||
| chr22:39786438
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.833-20829C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786438 | ||||||
| chr22:39786526
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG00597.hp1 HG00673.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.833-20917G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786526 | ||||||
| chr22:39786671
|
AC | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0121 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.833-21063delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786671 | ||||||
| chr22:39786676
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.833-21067A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786676 | ||||||
| chr22:39786694
|
A | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0106 | 2 | NA18982.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.833-21085T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786694 | ||||||
| chr22:39786704
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833-21095G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786704 | ||||||
| chr22:39786781
|
A | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-21172T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786781 | ||||||
| chr22:39786841
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.833-21232A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786841 | ||||||
| chr22:39786876
|
A | C | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.833-21267T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786876 | ||||||
| chr22:39786896
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-21287G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786896 | ||||||
| chr22:39786917
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.833-21308G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786917 | ||||||
| chr22:39787053
|
C | CTG | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(85): Show | 90 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.833-21446_833-2144 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39787053 | ||||||
| chr22:39787362
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.833-21753T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39787362 | ||||||
| chr22:39787413
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.833-21804G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39787413 | ||||||
| chr22:39787594
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.833-21985C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39787594 | ||||||
| chr22:39788003
|
A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-22394T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39788003 | ||||||
| chr22:39788466
|
C | T | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-22857G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39788466 | ||||||
| chr22:39788915
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(59): Show | 63 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.833-23306T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39788915 | ||||||
| chr22:39789150
|
A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-23541T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39789150 | ||||||
| chr22:39789279
|
G | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-23670C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39789279 | ||||||
| chr22:39789876
|
G | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-24267C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39789876 | ||||||
| chr22:39790175
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-24566G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790175 | ||||||
| chr22:39790181
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-24572G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790181 | ||||||
| chr22:39790261
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.833-24652T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790261 | ||||||
| chr22:39790461
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.833-24852T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790461 | ||||||
| chr22:39790541
|
C | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0029others(1): Show | 4 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-24932G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790541 | ||||||
| chr22:39790811
|
G | A | 4 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0001g0109others(1): Show | 4 | HG00621.hp2 HG02027.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.833-25202C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790811 | ||||||
| chr22:39791520
|
G | A | 1 | a0001c0004t0001g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.833-25911C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39791520 | ||||||
| chr22:39791842
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.833-26233A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39791842 | ||||||
| chr22:39792305
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-26696G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792305 | ||||||
| chr22:39792392
|
C | T | 1 | a0001c0008t0001g0140 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.833-26783G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792392 | ||||||
| chr22:39792421
|
C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-26812G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792421 | ||||||
| chr22:39792509
|
C | CTTAT | 2 | a0001c0001t0001g0070a0001c0001t0001g0114 | 2 | HG01069.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.833-26904_833-2690 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792509 | ||||||
| chr22:39792723
|
C | G | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-27114G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792723 | ||||||
| chr22:39792795
|
T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-27186A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792795 | ||||||
| chr22:39792817
|
C | CT | 22 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(19): Show | 23 | HG00621.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.833-27209dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792817 | ||||||
| chr22:39792921
|
T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-27312A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792921 | ||||||
| chr22:39792985
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.833-27376A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792985 | ||||||
| chr22:39793005
|
C | T | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-27396G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793005 | ||||||
| chr22:39793032
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.833-27423A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793032 | ||||||
| chr22:39793337
|
A | AGTT | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+27653_832+2765 others(7): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793337 | ||||||
| chr22:39793341
|
G | GT | 6 | a0001c0001t0001g0023a0001c0001t0001g0081a0001c0001t0001g0188others(3): Show | 6 | HG02717.hp1 HG03139.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.832+27651dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793341 | ||||||
| chr22:39793344
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.832+27649A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793344 | ||||||
| chr22:39793780
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.832+27213A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793780 | ||||||
| chr22:39793912
|
T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+27081A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793912 | ||||||
| chr22:39794182
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+26811C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794182 | ||||||
| chr22:39794352
|
T | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+26641A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794352 | ||||||
| chr22:39794613
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.832+26380A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794613 | ||||||
| chr22:39794629
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.832+26364G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794629 | ||||||
| chr22:39794631
|
T | C | 3 | a0001c0001t0001g0198a0001c0003t0001g0006a0003c0006t0001g0196 | 3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.832+26362A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794631 | ||||||
| chr22:39794803
|
C | CA | 5 | a0001c0001t0001g0037a0001c0001t0001g0081a0001c0001t0001g0173others(2): Show | 5 | HG02145.hp1 HG02559.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+26189dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794803 | ||||||
| chr22:39794803
|
CA | C | 9 | a0001c0001t0001g0177a0001c0001t0002g0155a0001c0001t0002g0162others(6): Show | 9 | HG02886.hp1 NA18522.hp2 NA18988.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+26189delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794803 | ||||||
| chr22:39794996
|
C | T | 2 | a0001c0001t0006g0214a0006c0005t0001g0019 | 2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.832+25997G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794996 | ||||||
| chr22:39795054
|
T | C | 8 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(5): Show | 8 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.832+25939A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795054 | ||||||
| chr22:39795194
|
G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+25799C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795194 | ||||||
| chr22:39795259
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+25734C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795259 | ||||||
| chr22:39795318
|
T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25675A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795318 | ||||||
| chr22:39795328
|
A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25665T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795328 | ||||||
| chr22:39795445
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25548C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795445 | ||||||
| chr22:39795515
|
C | A | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.832+25478G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795515 | ||||||
| chr22:39795586
|
C | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0073a0001c0001t0001g0074others(8): Show | 12 | HG00621.hp1 HG01993.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.832+25407G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795586 | ||||||
| chr22:39795594
|
AT | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(67): Show | 71 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.832+25398delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795594 | ||||||
| chr22:39795605
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.832+25388A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795605 | ||||||
| chr22:39795772
|
T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25221A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795772 | ||||||
| chr22:39795826
|
C | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25167G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795826 | ||||||
| chr22:39796018
|
A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+24975T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796018 | ||||||
| chr22:39796227
|
G | C | 2 | a0001c0001t0001g0098a0002c0002t0001g0211 | 2 | HG00642.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.832+24766C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796227 | ||||||
| chr22:39796261
|
C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+24732G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796261 | ||||||
| chr22:39796333
|
T | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+24660A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796333 | ||||||
| chr22:39796340
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+24653C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796340 | ||||||
| chr22:39796457
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0197 | 3 | HG02630.hp1 HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832+24536C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796457 | ||||||
| chr22:39796487
|
C | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0057others(3): Show | 6 | HG00639.hp1 HG01081.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+24506G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796487 | ||||||
| chr22:39796872
|
C | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0001t0001g0111 | 3 | HG00621.hp2 HG02027.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.832+24121G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796872 | ||||||
| chr22:39796874
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+24119C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796874 | ||||||
| chr22:39796897
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+24096C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796897 | ||||||
| chr22:39796922
|
T | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+24071A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796922 | ||||||
| chr22:39797099
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.832+23894G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797099 | ||||||
| chr22:39797266
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+23727G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797266 | ||||||
| chr22:39797498
|
C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+23495G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797498 | ||||||
| chr22:39797577
|
A | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+23416T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797577 | ||||||
| chr22:39797634
|
T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+23359A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797634 | ||||||
| chr22:39797923
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.832+23070C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797923 | ||||||
| chr22:39798376
|
G | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+22617C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798376 | ||||||
| chr22:39798575
|
C | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+22418G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798575 | ||||||
| chr22:39798593
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+22400C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798593 | ||||||
| chr22:39798637
|
A | G | 1 | a0001c0001t0001g0097 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.832+22356T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798637 | ||||||
| chr22:39798645
|
G | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.832+22348C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798645 | ||||||
| chr22:39798752
|
C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+22241G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798752 | ||||||
| chr22:39799012
|
C | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(2): Show | 5 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+21981G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799012 | ||||||
| chr22:39799204
|
G | A | 1 | a0004c0009t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.832+21789C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799204 | ||||||
| chr22:39799220
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0144 | 2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.832+21773G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799220 | ||||||
| chr22:39799230
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+21763C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799230 | ||||||
| chr22:39799377
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+21616C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799377 | ||||||
| chr22:39799388
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+21605G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799388 | ||||||
| chr22:39799460
|
G | A | 1 | a0002c0002t0001g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.832+21533C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799460 | ||||||
| chr22:39799666
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+21327G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799666 | ||||||
| chr22:39800059
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+20934A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39800059 | ||||||
| chr22:39800748
|
C | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+20245G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39800748 | ||||||
| chr22:39800749
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+20244C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39800749 | ||||||
| chr22:39800946
|
A | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(21): Show | 25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+20047T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39800946 | ||||||
| chr22:39801371
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.832+19622A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801371 | ||||||
| chr22:39801387
|
CAA | C | 3 | a0001c0001t0001g0014a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.832+19604_832+1960 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801387 | ||||||
| chr22:39801525
|
G | T | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+19468C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801525 | ||||||
| chr22:39801630
|
G | A | 38 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.832+19363C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801630 | ||||||
| chr22:39801678
|
G | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0195a0001c0001t0001g0199others(2): Show | 5 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+19315C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801678 | ||||||
| chr22:39801721
|
A | G | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+19272T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801721 | ||||||
| chr22:39801808
|
T | C | 3 | a0001c0001t0001g0014a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.832+19185A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801808 | ||||||
| chr22:39801925
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.832+19068C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801925 | ||||||
| chr22:39802435
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.832+18558A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39802435 | ||||||
| chr22:39802514
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.832+18479G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39802514 | ||||||
| chr22:39802949
|
G | A | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+18044C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39802949 | ||||||
| chr22:39803073
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.832+17920T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803073 | ||||||
| chr22:39803107
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.832+17886G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803107 | ||||||
| chr22:39803211
|
G | A | 1 | a0002c0002t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.832+17782C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803211 | ||||||
| chr22:39803286
|
C | T | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+17707G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803286 | ||||||
| chr22:39803287
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.832+17706C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803287 | ||||||
| chr22:39803334
|
C | T | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+17659G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803334 | ||||||
| chr22:39803535
|
A | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+17458T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803535 | ||||||
| chr22:39803780
|
T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+17213A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803780 | ||||||
| chr22:39803887
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+17106A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803887 | ||||||
| chr22:39804452
|
C | CA | 21 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0066others(18): Show | 21 | HG00621.hp2 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.832+16540dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39804452 | ||||||
| chr22:39804452
|
CA | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0064a0001c0001t0001g0110others(9): Show | 12 | HG01070.hp2 HG01167.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.832+16540delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39804452 | ||||||
| chr22:39804502
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0188others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+16491G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39804502 | ||||||
| chr22:39804525
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832+16468C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39804525 | ||||||
| chr22:39805034
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+15959G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805034 | ||||||
| chr22:39805073
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG02027.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.832+15920G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805073 | ||||||
| chr22:39805145
|
T | A | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+15848A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805145 | ||||||
| chr22:39805315
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.832+15678C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805315 | ||||||
| chr22:39805379
|
T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+15614A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805379 | ||||||
| chr22:39805386
|
G | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0006g0214others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+15607C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805386 | ||||||
| chr22:39805629
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.832+15364G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805629 | ||||||
| chr22:39805698
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0135a0001c0001t0001g0151others(1): Show | 4 | HG01257.hp2 HG01261.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+15295C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805698 | ||||||
| chr22:39806196
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+14797G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39806196 | ||||||
| chr22:39806404
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.832+14589G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39806404 | ||||||
| chr22:39806967
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.832+14026G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39806967 | ||||||
| chr22:39807241
|
C | T | 2 | a0001c0001t0002g0165a0001c0001t0004g0005 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.832+13752G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807241 | ||||||
| chr22:39807720
|
G | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+13273C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807720 | ||||||
| chr22:39807888
|
C | CGT | 11 | a0001c0001t0001g0014a0001c0001t0001g0059a0001c0001t0001g0068others(8): Show | 11 | HG00140.hp2 HG00639.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.832+13103_832+1310 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807888 | ||||||
| chr22:39807888
|
CGT | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0057 | 3 | HG00639.hp1 HG01081.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.832+13103_832+1310 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807888 | ||||||
| chr22:39807911
|
G | A | 2 | a0004c0009t0001g0153a0006c0005t0001g0019 | 2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+13082C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807911 | ||||||
| chr22:39807913
|
G | A | 36 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0045others(33): Show | 36 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.832+13080C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807913 | ||||||
| chr22:39807913
|
G | GTA | 3 | a0001c0001t0001g0009a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02055.hp1 HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+13078_832+1307 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807913 | ||||||
| chr22:39807915
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0046others(1): Show | 4 | HG02257.hp2 HG02896.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+13078T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807915 | ||||||
| chr22:39807917
|
A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+13076T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807917 | ||||||
| chr22:39808087
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+12906C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808087 | ||||||
| chr22:39808196
|
AC | A | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+12796delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808196 | ||||||
| chr22:39808278
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.832+12715G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808278 | ||||||
| chr22:39808324
|
G | A | 5 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158others(2): Show | 5 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+12669C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808324 | ||||||
| chr22:39808339
|
G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+12654C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808339 | ||||||
| chr22:39808426
|
A | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+12567T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808426 | ||||||
| chr22:39808437
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.832+12556A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808437 | ||||||
| chr22:39809493
|
G | A | 32 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(29): Show | 32 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.832+11500C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39809493 | ||||||
| chr22:39809728
|
C | T | 30 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(27): Show | 30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.832+11265G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39809728 | ||||||
| chr22:39810038
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.832+10955C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810038 | ||||||
| chr22:39810088
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02015.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.832+10905T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810088 | ||||||
| chr22:39810332
|
T | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0144 | 2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.832+10661A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810332 | ||||||
| chr22:39810430
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.832+10563T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810430 | ||||||
| chr22:39810536
|
T | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+10457A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810536 | ||||||
| chr22:39810582
|
C | T | 2 | a0001c0001t0002g0165a0001c0001t0004g0005 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.832+10411G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810582 | ||||||
| chr22:39810643
|
T | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+10350A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810643 | ||||||
| chr22:39810644
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.832+10349C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810644 | ||||||
| chr22:39810806
|
C | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(69): Show | 73 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.832+10187G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810806 | ||||||
| chr22:39811296
|
CA | C | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+9696delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811296 | ||||||
| chr22:39811348
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.832+9645G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811348 | ||||||
| chr22:39811367
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.832+9626G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811367 | ||||||
| chr22:39811396
|
C | G | 1 | a0001c0001t0002g0166 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.832+9597G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811396 | ||||||
| chr22:39811851
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+9142G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811851 | ||||||
| chr22:39811873
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.832+9120C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811873 | ||||||
| chr22:39811879
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+9114A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811879 | ||||||
| chr22:39811885
|
A | G | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.832+9108T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811885 | ||||||
| chr22:39811957
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.832+9036G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811957 | ||||||
| chr22:39812011
|
C | CA | 4 | a0001c0001t0001g0091a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+8981dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812011 | ||||||
| chr22:39812015
|
C | A | 4 | a0001c0001t0001g0091a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+8978G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812015 | ||||||
| chr22:39812015
|
C | CA | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 141 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.832+8977dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812015 | ||||||
| chr22:39812015
|
C | CAA | 5 | a0001c0001t0001g0033a0001c0001t0001g0076a0001c0001t0001g0145others(2): Show | 5 | HG00597.hp2 HG02647.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+8976_832+8977d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812015 | ||||||
| chr22:39812018
|
A | AC | 3 | a0001c0001t0001g0051a0001c0001t0001g0121a0001c0001t0002g0208 | 3 | HG00642.hp1 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.832+8974_832+8975i others(3): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812018 | ||||||
| chr22:39812025
|
A | AC | 50 | a0001c0001t0001g0023a0001c0001t0001g0045a0001c0001t0001g0048others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.832+8967dupG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812025 | ||||||
| chr22:39812220
|
T | C | 4 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0001g0109others(1): Show | 4 | HG00621.hp2 HG02027.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+8773A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812220 | ||||||
| chr22:39812269
|
A | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.832+8724T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812269 | ||||||
| chr22:39812449
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.832+8544T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812449 | ||||||
| chr22:39812843
|
C | T | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+8150G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812843 | ||||||
| chr22:39812970
|
G | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+8023C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812970 | ||||||
| chr22:39813026
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.832+7967C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813026 | ||||||
| chr22:39813069
|
C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+7924G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813069 | ||||||
| chr22:39813072
|
T | C | 38 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.832+7921A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813072 | ||||||
| chr22:39813113
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(25): Show | 29 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.832+7880A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813113 | ||||||
| chr22:39813170
|
A | G | 34 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.832+7823T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813170 | ||||||
| chr22:39813282
|
A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+7711T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813282 | ||||||
| chr22:39813925
|
C | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.832+7068G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813925 | ||||||
| chr22:39813992
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.832+7001C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813992 | ||||||
| chr22:39814052
|
T | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+6941A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814052 | ||||||
| chr22:39814135
|
T | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+6858A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814135 | ||||||
| chr22:39814295
|
C | CAAAAAAA others(6): Show |
1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+6685_832+6697d others(15): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | ||||||
| chr22:39814295
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0092a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG01891.hp2 HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+6684_832+6697d others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | ||||||
| chr22:39814295
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0002g0162others(1): Show | 4 | HG02886.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+6683_832+6697d others(17): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | ||||||
| chr22:39814295
|
C | CAAAAAAA others(9): Show |
22 | a0001c0001t0001g0173a0001c0001t0002g0154a0001c0001t0002g0155others(19): Show | 22 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.832+6682_832+6697d others(18): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | ||||||
| chr22:39814295
|
C | CAAAAAAA others(10): Show |
5 | a0001c0001t0002g0166a0001c0001t0002g0169a0001c0001t0002g0171others(2): Show | 5 | HG01106.hp2 HG02922.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+6697_832+6698i others(19): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | ||||||
| chr22:39814295
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+6697_832+6698i others(20): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | ||||||
| chr22:39814295
|
CA | C | 5 | a0001c0001t0001g0177a0001c0001t0001g0180a0001c0001t0001g0181others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+6697delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | ||||||
| chr22:39814312
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+6681A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814312 | ||||||
| chr22:39814364
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.832+6629C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814364 | ||||||
| chr22:39814428
|
C | G | 47 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0049others(44): Show | 47 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.832+6565G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814428 | ||||||
| chr22:39814438
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.832+6555G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814438 | ||||||
| chr22:39814536
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+6457T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814536 | ||||||
| chr22:39814540
|
CTATT | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+6449_832+6452d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814540 | ||||||
| chr22:39815015
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0129others(9): Show | 13 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.832+5978C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815015 | ||||||
| chr22:39815304
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+5689C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815304 | ||||||
| chr22:39815420
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+5573C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815420 | ||||||
| chr22:39815554
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0144 | 2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.832+5439A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815554 | ||||||
| chr22:39815602
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+5391G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815602 | ||||||
| chr22:39815638
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.832+5355G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815638 | ||||||
| chr22:39815733
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+5260C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815733 | ||||||
| chr22:39815804
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.832+5189C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815804 | ||||||
| chr22:39816009
|
G | A | 30 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(27): Show | 30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.832+4984C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816009 | ||||||
| chr22:39816041
|
G | A | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+4952C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816041 | ||||||
| chr22:39816354
|
C | T | 31 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(28): Show | 31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.832+4639G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816354 | ||||||
| chr22:39816666
|
C | T | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+4327G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816666 | ||||||
| chr22:39816678
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.832+4315T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816678 | ||||||
| chr22:39816762
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.832+4231T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816762 | ||||||
| chr22:39817238
|
A | C | 37 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(34): Show | 37 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.832+3755T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817238 | ||||||
| chr22:39817275
|
A | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(16): Show | 20 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.832+3718T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817275 | ||||||
| chr22:39817590
|
C | T | 8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0065others(5): Show | 8 | HG00438.hp2 HG02083.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.832+3403G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817590 | ||||||
| chr22:39817617
|
C | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.832+3376G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817617 | ||||||
| chr22:39817795
|
C | T | 16 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(13): Show | 17 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.832+3198G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817795 | ||||||
| chr22:39817832
|
T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+3161A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817832 | ||||||
| chr22:39817919
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+3074A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817919 | ||||||
| chr22:39818084
|
C | T | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+2909G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818084 | ||||||
| chr22:39818189
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.832+2804T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818189 | ||||||
| chr22:39818261
|
C | T | 9 | a0001c0001t0001g0066a0001c0001t0001g0077a0001c0001t0001g0083others(6): Show | 9 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+2732G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818261 | ||||||
| chr22:39818419
|
G | A | 9 | a0001c0001t0001g0066a0001c0001t0001g0077a0001c0001t0001g0083others(6): Show | 9 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+2574C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818419 | ||||||
| chr22:39818561
|
G | A | 1 | a0001c0003t0001g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.832+2432C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818561 | ||||||
| chr22:39818588
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+2405C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818588 | ||||||
| chr22:39818634
|
T | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0197 | 3 | HG02630.hp1 HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832+2359A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818634 | ||||||
| chr22:39819233
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+1760G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819233 | ||||||
| chr22:39819309
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0197 | 3 | HG02630.hp1 HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832+1684C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819309 | ||||||
| chr22:39819380
|
AC | A | 33 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(30): Show | 33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.832+1612delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819380 | ||||||
| chr22:39819381
|
C | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0006g0214others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+1612G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819381 | ||||||
| chr22:39819723
|
A | G | 33 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(30): Show | 33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.832+1270T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819723 | ||||||
| chr22:39819760
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0007g0025 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.832+1233C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819760 | ||||||
| chr22:39819923
|
A | G | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+1070T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819923 | ||||||
| chr22:39819991
|
T | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(81): Show | 86 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.832+1002A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819991 | ||||||
| chr22:39820313
|
T | C | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.832+680A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39820313 | ||||||
| chr22:39820388
|
T | A | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.832+605A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39820388 | ||||||
| chr22:39820547
|
T | C | 3 | a0001c0001t0001g0198a0001c0003t0001g0006a0003c0006t0001g0196 | 3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.832+446A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39820547 | ||||||
| chr22:39820604
|
C | T | 38 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.832+389G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39820604 | ||||||
| chr22:39821310
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.712-197G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39821310 | ||||||
| chr22:39821931
|
C | T | 31 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(28): Show | 31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.712-818G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39821931 | ||||||
| chr22:39821958
|
C | G | 1 | a0001c0001t0002g0161 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.712-845G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39821958 | ||||||
| chr22:39822011
|
C | T | 30 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(27): Show | 30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.712-898G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822011 | ||||||
| chr22:39822104
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.712-991T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822104 | ||||||
| chr22:39822108
|
C | A | 1 | a0001c0001t0001g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.712-995G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822108 | ||||||
| chr22:39822192
|
TC | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0021others(33): Show | 37 | HG00597.hp2 HG00673.hp1 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.712-1080delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822192 | ||||||
| chr22:39822631
|
C | T | 31 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(28): Show | 31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.712-1518G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822631 | ||||||
| chr22:39823378
|
T | G | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.712-2265A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823378 | ||||||
| chr22:39823405
|
C | T | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.712-2292G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823405 | ||||||
| chr22:39823450
|
T | A | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.712-2337A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823450 | ||||||
| chr22:39823788
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.712-2675A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823788 | ||||||
| chr22:39823798
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.712-2685T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823798 | ||||||
| chr22:39823882
|
A | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.712-2769T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823882 | ||||||
| chr22:39823923
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.712-2810G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823923 | ||||||
| chr22:39824128
|
G | A | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.712-3015C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824128 | ||||||
| chr22:39824201
|
C | CT | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 143 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.712-3089dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824201 | ||||||
| chr22:39824201
|
C | CTT | 30 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0038others(27): Show | 30 | HG00438.hp1 HG00621.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.712-3090_712-3089d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824201 | ||||||
| chr22:39824201
|
CT | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01943.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-3089delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824201 | ||||||
| chr22:39824279
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.712-3166C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824279 | ||||||
| chr22:39824354
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0060 | 3 | NA18942.hp1 NA18955.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.712-3241G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824354 | ||||||
| chr22:39824357
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.712-3244T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824357 | ||||||
| chr22:39824456
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.712-3343C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824456 | ||||||
| chr22:39824739
|
T | C | 33 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(30): Show | 33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.712-3626A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824739 | ||||||
| chr22:39824935
|
T | C | 5 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | HG00140.hp1 HG01070.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-3822A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824935 | ||||||
| chr22:39824994
|
GAAT | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0129 | 2 | NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.712-3884_712-3882d others(5): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824994 | ||||||
| chr22:39825112
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.712-3999G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825112 | ||||||
| chr22:39825366
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.712-4253A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825366 | ||||||
| chr22:39825475
|
C | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.712-4362G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825475 | ||||||
| chr22:39825708
|
T | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.712-4595A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825708 | ||||||
| chr22:39825995
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.712-4882G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825995 | ||||||
| chr22:39826126
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0004t0001g0093others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-5013C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826126 | ||||||
| chr22:39826196
|
T | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.712-5083A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826196 | ||||||
| chr22:39826244
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.712-5131G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826244 | ||||||
| chr22:39826307
|
G | T | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.712-5194C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826307 | ||||||
| chr22:39826308
|
G | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0036others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-5195C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826308 | ||||||
| chr22:39826500
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.712-5387C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826500 | ||||||
| chr22:39826905
|
CTCTG | C | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.712-5796_712-5793d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826905 | ||||||
| chr22:39827014
|
A | AT | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0121others(3): Show | 6 | HG02135.hp1 HG02148.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-5902dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827014 | ||||||
| chr22:39827084
|
C | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0178 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.712-5971G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827084 | ||||||
| chr22:39827117
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.712-6004C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827117 | ||||||
| chr22:39827205
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0006g0214 | 2 | HG02886.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.712-6092G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827205 | ||||||
| chr22:39827250
|
C | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0065a0001c0001t0001g0104 | 3 | HG02083.hp2 NA18947.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.712-6137G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827250 | ||||||
| chr22:39827262
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.712-6149C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827262 | ||||||
| chr22:39828021
|
G | A | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.712-6908C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828021 | ||||||
| chr22:39828162
|
A | G | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.712-7049T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828162 | ||||||
| chr22:39828743
|
T | A | 3 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0145 | 3 | HG00597.hp2 HG00673.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.711+7097A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828743 | ||||||
| chr22:39828839
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.711+7001T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828839 | ||||||
| chr22:39828919
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.711+6921C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828919 | ||||||
| chr22:39828998
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.711+6842C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828998 | ||||||
| chr22:39829010
|
G | A | 1 | a0002c0002t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.711+6830C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829010 | ||||||
| chr22:39829082
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG00597.hp1 HG00673.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.711+6758T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829082 | ||||||
| chr22:39829142
|
C | T | 4 | a0001c0001t0001g0062a0001c0001t0001g0103a0001c0001t0001g0109others(1): Show | 4 | HG00621.hp2 HG02027.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+6698G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829142 | ||||||
| chr22:39829267
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.711+6573C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829267 | ||||||
| chr22:39829379
|
C | CA | 9 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0042others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.711+6460dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829379 | ||||||
| chr22:39829379
|
CA | C | 53 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0050others(50): Show | 53 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.711+6460delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829379 | ||||||
| chr22:39829648
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.711+6192C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829648 | ||||||
| chr22:39829790
|
C | CAATA | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(58): Show | 63 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.711+6046_711+6049d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | ||||||
| chr22:39829790
|
C | CAATAAAT others(1): Show |
9 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0032others(6): Show | 9 | HG01891.hp1 HG02055.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.711+6042_711+6049d others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | ||||||
| chr22:39829790
|
C | CAATAAAT others(5): Show |
3 | a0001c0001t0002g0171a0001c0004t0001g0093a0004c0009t0001g0153 | 3 | HG02572.hp2 HG02922.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.711+6038_711+6049d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | ||||||
| chr22:39829790
|
C | CAATAAAT others(9): Show |
23 | a0001c0001t0001g0009a0001c0001t0002g0154a0001c0001t0002g0155others(20): Show | 23 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.711+6034_711+6049d others(18): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | ||||||
| chr22:39829790
|
C | CAATAAAT others(13): Show |
4 | a0001c0001t0002g0165a0001c0001t0002g0169a0001c0001t0002g0170others(1): Show | 4 | HG04115.hp2 NA18988.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+6030_711+6049d others(22): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | ||||||
| chr22:39829790
|
C | CAATAAAT others(17): Show |
3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0167 | 3 | NA18998.hp2 NA19002.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.711+6026_711+6049d others(26): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | ||||||
| chr22:39829973
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.711+5867A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829973 | ||||||
| chr22:39830170
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.711+5670C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830170 | ||||||
| chr22:39830236
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0004t0001g0093others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+5604G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830236 | ||||||
| chr22:39830357
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.711+5483C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830357 | ||||||
| chr22:39830661
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.711+5179T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830661 | ||||||
| chr22:39830677
|
A | T | 1 | a0001c0001t0002g0162 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.711+5163T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830677 | ||||||
| chr22:39830697
|
T | C | 38 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.711+5143A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830697 | ||||||
| chr22:39830786
|
C | T | 31 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(28): Show | 31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.711+5054G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830786 | ||||||
| chr22:39831199
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.711+4641T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831199 | ||||||
| chr22:39831216
|
A | G | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.711+4624T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831216 | ||||||
| chr22:39831261
|
C | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.711+4579G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831261 | ||||||
| chr22:39831271
|
A | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0023others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+4569T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831271 | ||||||
| chr22:39831467
|
A | G | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.711+4373T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831467 | ||||||
| chr22:39831537
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.711+4303A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831537 | ||||||
| chr22:39831553
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.711+4287C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831553 | ||||||
| chr22:39831699
|
G | A | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.711+4141C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831699 | ||||||
| chr22:39831855
|
T | C | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.711+3985A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831855 | ||||||
| chr22:39832226
|
G | A | 1 | a0001c0008t0001g0140 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.711+3614C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832226 | ||||||
| chr22:39832360
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.711+3480C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832360 | ||||||
| chr22:39832369
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.711+3471G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832369 | ||||||
| chr22:39832846
|
G | A | 27 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.711+2994C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832846 | ||||||
| chr22:39832889
|
A | G | 1 | a0001c0001t0002g0166 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.711+2951T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832889 | ||||||
| chr22:39833230
|
C | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.711+2610G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833230 | ||||||
| chr22:39833275
|
C | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0081others(1): Show | 4 | HG02258.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+2565G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833275 | ||||||
| chr22:39833430
|
G | T | 16 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(13): Show | 17 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.711+2410C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833430 | ||||||
| chr22:39833589
|
A | T | 54 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 55 | HG00597.hp2 HG00642.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.711+2251T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833589 | ||||||
| chr22:39833670
|
A | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.711+2170T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833670 | ||||||
| chr22:39833745
|
A | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.711+2095T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833745 | ||||||
| chr22:39833769
|
A | T | 38 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(35): Show | 38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.711+2071T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833769 | ||||||
| chr22:39833941
|
C | CA | 99 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(96): Show | 100 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.711+1898dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | ||||||
| chr22:39833941
|
C | CAA | 8 | a0001c0001t0001g0009a0001c0001t0001g0081a0001c0001t0001g0173others(5): Show | 8 | HG00735.hp2 HG00738.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.711+1897_711+1898d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | ||||||
| chr22:39833941
|
CAAAA | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0131others(6): Show | 10 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+1895_711+1898d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | ||||||
| chr22:39833941
|
CAAAAA | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0054a0001c0001t0001g0057others(2): Show | 5 | HG00639.hp1 HG00639.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+1894_711+1898d others(7): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | ||||||
| chr22:39833941
|
CAAAAAA | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(61): Show | 65 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.711+1893_711+1898d others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | ||||||
| chr22:39834151
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.711+1689A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39834151 | ||||||
| chr22:39834902
|
T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.711+938A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39834902 | ||||||
| chr22:39835057
|
A | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.711+783T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39835057 | ||||||
| chr22:39835645
|
A | T | 1 | a0001c0001t0004g0005 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.711+195T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39835645 | ||||||
| chr22:39835653
|
C | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.711+187G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39835653 | ||||||
| chr22:39835834
|
A | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.711+6T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39835834 | ||||||
| chr22:39836413
|
T | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-455A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39836413 | ||||||
| chr22:39836668
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.593-710T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39836668 | ||||||
| chr22:39836711
|
G | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-753C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39836711 | ||||||
| chr22:39837306
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.593-1348C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39837306 | ||||||
| chr22:39837589
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.593-1631C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39837589 | ||||||
| chr22:39838000
|
A | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 5 | HG00140.hp1 HG01070.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-2042T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39838000 | ||||||
| chr22:39838091
|
T | C | 34 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.593-2133A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39838091 | ||||||
| chr22:39838199
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-2241A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39838199 | ||||||
| chr22:39838219
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-2261C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39838219 | ||||||
| chr22:39839279
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0178 | 2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.593-3321T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839279 | ||||||
| chr22:39839408
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.593-3450A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839408 | ||||||
| chr22:39839434
|
C | T | 1 | a0004c0009t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.593-3476G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839434 | ||||||
| chr22:39839682
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.593-3724G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839682 | ||||||
| chr22:39839831
|
T | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.593-3873A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839831 | ||||||
| chr22:39840030
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-4072A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840030 | ||||||
| chr22:39840593
|
AACAG | A | 9 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0204others(6): Show | 9 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.593-4639_593-4636d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840593 | ||||||
| chr22:39840759
|
CT | C | 37 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(34): Show | 37 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.593-4802delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840759 | ||||||
| chr22:39840777
|
C | T | 30 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(27): Show | 30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.593-4819G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840777 | ||||||
| chr22:39840877
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.593-4919G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840877 | ||||||
| chr22:39840961
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.593-5003G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840961 | ||||||
| chr22:39841030
|
G | A | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-5072C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841030 | ||||||
| chr22:39841134
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.593-5176A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841134 | ||||||
| chr22:39841193
|
A | G | 34 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.593-5235T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841193 | ||||||
| chr22:39841566
|
T | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-5608A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841566 | ||||||
| chr22:39841605
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.593-5647G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841605 | ||||||
| chr22:39841624
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.593-5666C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841624 | ||||||
| chr22:39841778
|
G | T | 4 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0208others(1): Show | 4 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-5820C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841778 | ||||||
| chr22:39841782
|
C | A | 4 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0208others(1): Show | 4 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-5824G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841782 | ||||||
| chr22:39841832
|
C | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-5874G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841832 | ||||||
| chr22:39841907
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0106 | 2 | NA18982.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.593-5949G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841907 | ||||||
| chr22:39842197
|
A | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-6239T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842197 | ||||||
| chr22:39842394
|
C | A | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.593-6436G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842394 | ||||||
| chr22:39842397
|
T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.593-6439A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842397 | ||||||
| chr22:39842524
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-6566G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842524 | ||||||
| chr22:39842536
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-6578C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842536 | ||||||
| chr22:39842799
|
G | A | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-6841C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842799 | ||||||
| chr22:39843053
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0121 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.593-7095T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843053 | ||||||
| chr22:39843100
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-7142G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843100 | ||||||
| chr22:39843174
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.593-7216C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843174 | ||||||
| chr22:39843354
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0061 | 2 | NA18984.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.593-7396C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843354 | ||||||
| chr22:39843362
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-7404T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843362 | ||||||
| chr22:39843402
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-7444A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843402 | ||||||
| chr22:39843466
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.593-7508C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843466 | ||||||
| chr22:39843478
|
T | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-7520A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843478 | ||||||
| chr22:39843567
|
A | G | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-7609T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843567 | ||||||
| chr22:39843606
|
A | G | 53 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0049others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.593-7648T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843606 | ||||||
| chr22:39844025
|
G | GTGTACAA others(43): Show |
1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.593-8117_593-8068d others(52): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844025 | ||||||
| chr22:39844025
|
GTGTACAA others(43): Show |
G | 1 | a0001c0001t0001g0133 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.593-8117_593-8068d others(52): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844025 | ||||||
| chr22:39844196
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.593-8238C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844196 | ||||||
| chr22:39844494
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(84): Show | 89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.593-8536T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844494 | ||||||
| chr22:39844521
|
A | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.593-8563T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844521 | ||||||
| chr22:39844528
|
T | C | 34 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.593-8570A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844528 | ||||||
| chr22:39844569
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.593-8611A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844569 | ||||||
| chr22:39844572
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.593-8614A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844572 | ||||||
| chr22:39844700
|
T | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-8742A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844700 | ||||||
| chr22:39844712
|
G | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-8754C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844712 | ||||||
| chr22:39844798
|
G | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(33): Show | 36 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.593-8840C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844798 | ||||||
| chr22:39844911
|
C | G | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.593-8953G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844911 | ||||||
| chr22:39845039
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG00597.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.593-9081A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845039 | ||||||
| chr22:39845074
|
T | TA | 6 | a0001c0001t0002g0165a0001c0001t0008g0015a0001c0004t0001g0093others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.593-9117dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845074 | ||||||
| chr22:39845180
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.593-9222T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845180 | ||||||
| chr22:39845208
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.593-9250A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845208 | ||||||
| chr22:39845283
|
C | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.593-9325G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845283 | ||||||
| chr22:39845473
|
C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-9515G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845473 | ||||||
| chr22:39845622
|
T | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-9664A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845622 | ||||||
| chr22:39845657
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(82): Show | 87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.593-9699C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845657 | ||||||
| chr22:39845907
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.593-9949A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845907 | ||||||
| chr22:39846005
|
C | A | 1 | a0001c0001t0002g0205 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.593-10047G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846005 | ||||||
| chr22:39846063
|
C | A | 3 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0001t0001g0111 | 3 | HG00621.hp2 HG02027.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.593-10105G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846063 | ||||||
| chr22:39846378
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.593-10420A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846378 | ||||||
| chr22:39846507
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.593-10549C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846507 | ||||||
| chr22:39846546
|
T | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(32): Show | 35 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.593-10588A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846546 | ||||||
| chr22:39846860
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-10902C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846860 | ||||||
| chr22:39847084
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.593-11126C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847084 | ||||||
| chr22:39847140
|
A | G | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.593-11182T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847140 | ||||||
| chr22:39847143
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-11185C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847143 | ||||||
| chr22:39847382
|
A | AG | 7 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0047others(4): Show | 7 | HG01192.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-11425dupC | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847382 | ||||||
| chr22:39847466
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.593-11508G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847466 | ||||||
| chr22:39847708
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0121 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.593-11750C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847708 | ||||||
| chr22:39847890
|
G | C | 34 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.593-11932C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847890 | ||||||
| chr22:39847965
|
G | A | 3 | a0001c0001t0001g0198a0001c0003t0001g0006a0003c0006t0001g0196 | 3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.593-12007C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847965 | ||||||
| chr22:39848008
|
C | A | 1 | a0002c0002t0001g0190 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.593-12050G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848008 | ||||||
| chr22:39848277
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.593-12319G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848277 | ||||||
| chr22:39848278
|
G | A | 1 | a0001c0004t0001g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.593-12320C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848278 | ||||||
| chr22:39848300
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.593-12342G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848300 | ||||||
| chr22:39848572
|
C | T | 1 | a0002c0002t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.593-12614G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848572 | ||||||
| chr22:39848634
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.593-12676A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848634 | ||||||
| chr22:39848879
|
C | T | 5 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158others(2): Show | 5 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+12886G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848879 | ||||||
| chr22:39848998
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG02886.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.592+12767G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848998 | ||||||
| chr22:39849418
|
T | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.592+12347A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39849418 | ||||||
| chr22:39849706
|
T | C | 1 | a0001c0001t0002g0172 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.592+12059A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39849706 | ||||||
| chr22:39849820
|
G | A | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+11945C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39849820 | ||||||
| chr22:39849919
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0008g0015 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.592+11846G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39849919 | ||||||
| chr22:39850103
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.592+11662T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850103 | ||||||
| chr22:39850257
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.592+11508A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850257 | ||||||
| chr22:39850310
|
A | G | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+11455T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850310 | ||||||
| chr22:39850381
|
T | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | NA18977.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.592+11384A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850381 | ||||||
| chr22:39850434
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.592+11331A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850434 | ||||||
| chr22:39850674
|
C | T | 1 | a0002c0002t0001g0193 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.592+11091G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850674 | ||||||
| chr22:39850833
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.592+10932C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850833 | ||||||
| chr22:39850906
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.592+10859G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850906 | ||||||
| chr22:39851111
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+10654A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39851111 | ||||||
| chr22:39851895
|
G | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+9870C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39851895 | ||||||
| chr22:39852170
|
C | CA | 5 | a0001c0001t0001g0130a0001c0001t0001g0198a0001c0001t0004g0005others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+9594dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852170 | ||||||
| chr22:39852250
|
G | A | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+9515C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852250 | ||||||
| chr22:39852337
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+9428T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852337 | ||||||
| chr22:39852622
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.592+9143G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852622 | ||||||
| chr22:39852678
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.592+9087A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852678 | ||||||
| chr22:39852980
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.592+8785A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852980 | ||||||
| chr22:39853368
|
T | TA | 13 | a0001c0001t0001g0002a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 14 | HG00621.hp1 HG01993.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.592+8396dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853368 | ||||||
| chr22:39853576
|
C | A | 3 | a0001c0001t0001g0014a0001c0001t0006g0214a0001c0001t0008g0015 | 3 | HG02559.hp1 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.592+8189G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853576 | ||||||
| chr22:39853576
|
CTTATTA | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+8183_592+8188d others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853576 | ||||||
| chr22:39853579
|
A | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0055others(1): Show | 4 | HG03490.hp2 HG03492.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+8186T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853579 | ||||||
| chr22:39853635
|
G | A | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.592+8130C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853635 | ||||||
| chr22:39853850
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.592+7915G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853850 | ||||||
| chr22:39853978
|
G | A | 1 | a0001c0004t0001g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.592+7787C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853978 | ||||||
| chr22:39854142
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.592+7623C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854142 | ||||||
| chr22:39854218
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.592+7547T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854218 | ||||||
| chr22:39854320
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.592+7445A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854320 | ||||||
| chr22:39854819
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.592+6946G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854819 | ||||||
| chr22:39854865
|
C | G | 35 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(32): Show | 35 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.592+6900G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854865 | ||||||
| chr22:39855023
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+6742T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855023 | ||||||
| chr22:39855247
|
A | T | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+6518T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855247 | ||||||
| chr22:39855270
|
A | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.592+6495T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855270 | ||||||
| chr22:39855487
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+6278G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855487 | ||||||
| chr22:39855589
|
TA | T | 31 | a0001c0001t0001g0009a0001c0001t0002g0154a0001c0001t0002g0155others(28): Show | 31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.592+6175delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855589 | ||||||
| chr22:39855830
|
A | T | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.592+5935T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855830 | ||||||
| chr22:39855914
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | NA18967.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.592+5851T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855914 | ||||||
| chr22:39855990
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.592+5775C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855990 | ||||||
| chr22:39855999
|
C | T | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.592+5766G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855999 | ||||||
| chr22:39856000
|
G | A | 2 | a0001c0001t0002g0165a0001c0001t0004g0005 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.592+5765C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856000 | ||||||
| chr22:39856012
|
C | T | 2 | a0001c0001t0001g0055a0006c0005t0001g0019 | 2 | HG01891.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.592+5753G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856012 | ||||||
| chr22:39856215
|
G | A | 9 | a0001c0001t0001g0152a0001c0001t0001g0195a0001c0001t0001g0197others(6): Show | 9 | HG00639.hp2 HG01496.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.592+5550C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856215 | ||||||
| chr22:39856274
|
C | CA | 35 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0001g0198others(32): Show | 35 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.592+5490dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856274 | ||||||
| chr22:39856274
|
CA | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0052a0001c0001t0001g0092others(3): Show | 6 | HG00673.hp2 HG01069.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+5490delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856274 | ||||||
| chr22:39856413
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.592+5352G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856413 | ||||||
| chr22:39856536
|
T | C | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.592+5229A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856536 | ||||||
| chr22:39856560
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.592+5205A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856560 | ||||||
| chr22:39856813
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.592+4952T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856813 | ||||||
| chr22:39856852
|
CA | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(3): Show | 6 | HG00323.hp2 HG01069.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+4912delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856852 | ||||||
| chr22:39856865
|
A | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+4900T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856865 | ||||||
| chr22:39856867
|
AAG | A | 29 | a0001c0001t0001g0173a0001c0001t0002g0154a0001c0001t0002g0155others(26): Show | 29 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.592+4896_592+4897d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856867 | ||||||
| chr22:39856869
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0023others(2): Show | 5 | HG02055.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+4896C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856869 | ||||||
| chr22:39856873
|
G | A | 34 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0154others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.592+4892C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856873 | ||||||
| chr22:39857150
|
G | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+4615C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857150 | ||||||
| chr22:39857360
|
C | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.592+4405G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857360 | ||||||
| chr22:39857412
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0003t0001g0006others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+4353G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857412 | ||||||
| chr22:39857443
|
CA | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0014others(22): Show | 26 | HG01496.hp1 HG02015.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.592+4321delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857443 | ||||||
| chr22:39857443
|
CAA | C | 22 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0029others(19): Show | 23 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+4320_592+4321d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857443 | ||||||
| chr22:39857471
|
A | AAAAT | 5 | a0001c0001t0002g0163a0001c0001t0002g0170a0001c0001t0002g0171others(2): Show | 5 | HG01106.hp2 HG02293.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+4293_592+4294i others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857471 | ||||||
| chr22:39857471
|
A | AAAT | 24 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(21): Show | 24 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.592+4293_592+4294i others(5): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857471 | ||||||
| chr22:39857471
|
A | AT | 16 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0082others(13): Show | 17 | HG00642.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.592+4293_592+4294i others(3): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857471 | ||||||
| chr22:39857471
|
A | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(118): Show | 123 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.592+4294T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857471 | ||||||
| chr22:39857712
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+4053T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857712 | ||||||
| chr22:39857911
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.592+3854C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857911 | ||||||
| chr22:39858034
|
T | G | 1 | a0004c0009t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.592+3731A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39858034 | ||||||
| chr22:39859087
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.592+2678C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39859087 | ||||||
| chr22:39859242
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.592+2523A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39859242 | ||||||
| chr22:39859270
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.592+2495T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39859270 | ||||||
| chr22:39859804
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0060 | 2 | NA18942.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.592+1961C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39859804 | ||||||
| chr22:39860144
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.592+1621A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860144 | ||||||
| chr22:39860158
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.592+1607A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860158 | ||||||
| chr22:39860480
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.592+1285G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860480 | ||||||
| chr22:39860481
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 68 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.592+1284C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860481 | ||||||
| chr22:39860660
|
C | A | 3 | a0002c0002t0001g0176a0002c0002t0001g0190a0002c0002t0001g0193 | 3 | HG00735.hp2 HG01943.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.592+1105G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860660 | ||||||
| chr22:39861018
|
G | T | 1 | a0001c0001t0001g0048 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.592+747C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861018 | ||||||
| chr22:39861054
|
T | C | 1 | a0002c0002t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.592+711A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861054 | ||||||
| chr22:39861430
|
C | T | 2 | a0002c0002t0001g0210a0002c0002t0001g0211 | 2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.592+335G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861430 | ||||||
| chr22:39861455
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.592+310C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861455 | ||||||
| chr22:39861535
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.592+230C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861535 | ||||||
| chr22:39861620
|
G | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0122 | 3 | HG01168.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.592+145C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861620 | ||||||
| chr22:39862081
|
A | T | 11 | a0001c0001t0001g0066a0001c0001t0001g0077a0001c0001t0001g0083others(8): Show | 11 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-74T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862081 | ||||||
| chr22:39862100
|
T | A | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-93A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862100 | ||||||
| chr22:39862150
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.350-143A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862150 | ||||||
| chr22:39862373
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350-366G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862373 | ||||||
| chr22:39862411
|
G | C | 2 | a0001c0001t0001g0009a0004c0009t0001g0153 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.350-404C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862411 | ||||||
| chr22:39862532
|
G | A | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-525C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862532 | ||||||
| chr22:39862546
|
C | CA | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 17 | HG02258.hp1 HG02258.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-540dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862546 | ||||||
| chr22:39862560
|
AAAAG | A | 5 | a0001c0001t0001g0105a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-557_350-554del others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862560 | ||||||
| chr22:39862563
|
AG | A | 26 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0002g0155others(23): Show | 26 | HG00642.hp1 HG00738.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.350-557delC | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862563 | ||||||
| chr22:39862564
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0002g0154others(6): Show | 9 | HG01891.hp1 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-557C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862564 | ||||||
| chr22:39862661
|
C | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350-654G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862661 | ||||||
| chr22:39862722
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-715A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862722 | ||||||
| chr22:39862770
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.350-763T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862770 | ||||||
| chr22:39862986
|
G | A | 1 | a0001c0003t0001g0007 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.350-979C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862986 | ||||||
| chr22:39863075
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.350-1068T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863075 | ||||||
| chr22:39863316
|
A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-1309T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863316 | ||||||
| chr22:39863531
|
A | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0121 | 2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.350-1524T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863531 | ||||||
| chr22:39863798
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0034 | 2 | NA18979.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.350-1791C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863798 | ||||||
| chr22:39863856
|
C | T | 33 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0173others(30): Show | 33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.350-1849G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863856 | ||||||
| chr22:39863906
|
G | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350-1899C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863906 | ||||||
| chr22:39864017
|
T | TA | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0189 | 3 | HG01884.hp2 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.350-2011dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39864017 | ||||||
| chr22:39864457
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-2450A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39864457 | ||||||
| chr22:39864591
|
A | G | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-2584T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39864591 | ||||||
| chr22:39864627
|
T | C | 3 | a0001c0001t0001g0014a0001c0004t0001g0093a0001c0004t0001g0094 | 3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.350-2620A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39864627 | ||||||
| chr22:39865271
|
C | T | 4 | a0001c0001t0002g0156a0001c0001t0002g0158a0001c0001t0002g0159others(1): Show | 4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-3264G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865271 | ||||||
| chr22:39865414
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.350-3407T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865414 | ||||||
| chr22:39865450
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350-3443T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865450 | ||||||
| chr22:39865551
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-3544G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865551 | ||||||
| chr22:39865631
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.350-3624G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865631 | ||||||
| chr22:39866380
|
G | A | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.350-4373C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866380 | ||||||
| chr22:39866477
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(82): Show | 87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.350-4470T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866477 | ||||||
| chr22:39866502
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.350-4495C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866502 | ||||||
| chr22:39866795
|
T | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-4788A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866795 | ||||||
| chr22:39866975
|
C | T | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-4968G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866975 | ||||||
| chr22:39867063
|
C | T | 1 | a0001c0003t0001g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.350-5056G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867063 | ||||||
| chr22:39867115
|
G | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(17): Show | 21 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.350-5108C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867115 | ||||||
| chr22:39867280
|
T | C | 1 | a0004c0009t0001g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.350-5273A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867280 | ||||||
| chr22:39867355
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-5348A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867355 | ||||||
| chr22:39867499
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350-5492C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867499 | ||||||
| chr22:39867525
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-5518G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867525 | ||||||
| chr22:39867642
|
C | T | 8 | a0001c0001t0002g0155a0001c0001t0002g0162a0001c0001t0002g0163others(5): Show | 8 | NA18988.hp2 NA18998.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-5635G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867642 | ||||||
| chr22:39867993
|
C | T | 20 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0053others(17): Show | 20 | HG00438.hp2 HG00639.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.350-5986G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867993 | ||||||
| chr22:39868281
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.350-6274A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868281 | ||||||
| chr22:39868329
|
C | A | 1 | a0001c0001t0001g0199 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.350-6322G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868329 | ||||||
| chr22:39868350
|
T | TA | 5 | a0001c0001t0001g0023a0001c0001t0001g0051a0001c0001t0001g0150others(2): Show | 5 | HG00642.hp2 HG01168.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-6344dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868350 | ||||||
| chr22:39868350
|
T | TAA | 31 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(28): Show | 31 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.350-6345_350-6344d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868350 | ||||||
| chr22:39868350
|
TA | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0043others(10): Show | 13 | HG02055.hp1 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-6344delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868350 | ||||||
| chr22:39868547
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(84): Show | 89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.350-6540G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868547 | ||||||
| chr22:39868580
|
G | C | 39 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.350-6573C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868580 | ||||||
| chr22:39869098
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.350-7091C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869098 | ||||||
| chr22:39869121
|
T | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0060 | 3 | NA18942.hp1 NA18955.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.350-7114A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869121 | ||||||
| chr22:39869246
|
G | A | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-7239C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869246 | ||||||
| chr22:39869586
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-7579C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869586 | ||||||
| chr22:39869637
|
TA | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0051others(6): Show | 9 | HG01943.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.350-7631delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869637 | ||||||
| chr22:39869650
|
A | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350-7643T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869650 | ||||||
| chr22:39869910
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.350-7903T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869910 | ||||||
| chr22:39869983
|
C | CTTTA | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.350-7980_350-7977d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869983 | ||||||
| chr22:39869983
|
C | CTTTATTT others(1): Show |
20 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0038others(17): Show | 20 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.350-7984_350-7977d others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869983 | ||||||
| chr22:39869983
|
C | CTTTATTT others(5): Show |
8 | a0001c0001t0001g0026a0001c0001t0001g0072a0001c0001t0001g0077others(5): Show | 8 | HG00735.hp1 HG01081.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-7988_350-7977d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869983 | ||||||
| chr22:39869983
|
CTTTA | C | 10 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0057others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-7980_350-7977d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869983 | ||||||
| chr22:39869998
|
T | TATTTATT others(1): Show |
15 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(12): Show | 16 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.350-7992_350-7991i others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869998 | ||||||
| chr22:39870121
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.350-8114T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870121 | ||||||
| chr22:39870268
|
CAA | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0031others(1): Show | 5 | HG02055.hp2 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-8263_350-8262d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870268 | ||||||
| chr22:39870368
|
A | G | 2 | a0002c0002t0001g0191a0002c0002t0001g0192 | 2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.350-8361T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870368 | ||||||
| chr22:39870457
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.350-8450T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870457 | ||||||
| chr22:39870639
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.350-8632A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870639 | ||||||
| chr22:39871172
|
A | AAAAT | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(44): Show | 49 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.350-9169_350-9166d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | ||||||
| chr22:39871172
|
A | AAAATAAA others(1): Show |
19 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0036others(16): Show | 20 | HG01257.hp1 HG01993.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.350-9173_350-9166d others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | ||||||
| chr22:39871172
|
A | AAAATAAA others(5): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG02027.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.350-9177_350-9166d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | ||||||
| chr22:39871172
|
AAAAT | A | 38 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0048others(35): Show | 38 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.350-9169_350-9166d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | ||||||
| chr22:39871172
|
AAAATAAA others(1): Show |
A | 8 | a0001c0001t0001g0020a0001c0001t0001g0062a0001c0001t0001g0107others(5): Show | 8 | HG00438.hp2 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-9173_350-9166d others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | ||||||
| chr22:39871172
|
AAAATAAA others(5): Show |
A | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0003t0001g0006others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-9177_350-9166d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | ||||||
| chr22:39871172
|
AAAATAAA others(13): Show |
A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-9185_350-9166d others(22): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | ||||||
| chr22:39871337
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.350-9330G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871337 | ||||||
| chr22:39871471
|
G | A | 1 | a0001c0001t0001g0003 | 2 | NA18979.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.350-9464C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871471 | ||||||
| chr22:39871839
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0173 | 2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350-9832T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871839 | ||||||
| chr22:39872283
|
T | C | 2 | a0001c0003t0001g0007a0001c0003t0001g0008 | 2 | HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.350-10276A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872283 | ||||||
| chr22:39872813
|
A | G | 41 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0020others(38): Show | 41 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.350-10806T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872813 | ||||||
| chr22:39872850
|
C | CT | 5 | a0001c0001t0001g0048a0001c0001t0001g0081a0001c0001t0001g0131others(2): Show | 5 | HG04199.hp2 NA18947.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-10844dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872850 | ||||||
| chr22:39872852
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.350-10845A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872852 | ||||||
| chr22:39872994
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.350-10987A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872994 | ||||||
| chr22:39873434
|
G | T | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-11427C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39873434 | ||||||
| chr22:39874005
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.350-11998G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874005 | ||||||
| chr22:39874023
|
A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-12016T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874023 | ||||||
| chr22:39874429
|
C | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.350-12422G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874429 | ||||||
| chr22:39874463
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.350-12456G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874463 | ||||||
| chr22:39874609
|
CTATAA | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-12607_350-1260 others(9): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874609 | ||||||
| chr22:39874724
|
T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+12676A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874724 | ||||||
| chr22:39874924
|
A | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+12476T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874924 | ||||||
| chr22:39875310
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349+12090C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875310 | ||||||
| chr22:39875492
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.349+11908C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875492 | ||||||
| chr22:39875610
|
C | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(100): Show | 104 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.349+11790G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875610 | ||||||
| chr22:39875686
|
C | T | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.349+11714G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875686 | ||||||
| chr22:39875727
|
T | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0142 | 4 | NA18979.hp2 NA18984.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+11673A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875727 | ||||||
| chr22:39875818
|
A | G | 35 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0023others(32): Show | 35 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.349+11582T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875818 | ||||||
| chr22:39875836
|
G | A | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.349+11564C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875836 | ||||||
| chr22:39876138
|
C | A | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.349+11262G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876138 | ||||||
| chr22:39876455
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+10945C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876455 | ||||||
| chr22:39876514
|
T | TA | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02145.hp2 HG03017.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+10885dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876514 | ||||||
| chr22:39876514
|
TA | T | 9 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0126others(6): Show | 9 | HG00323.hp1 HG01884.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.349+10885delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876514 | ||||||
| chr22:39876530
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0023a0004c0009t0001g0153 | 3 | HG02896.hp2 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.349+10870T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876530 | ||||||
| chr22:39877025
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.349+10375T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877025 | ||||||
| chr22:39877137
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.349+10263T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877137 | ||||||
| chr22:39877239
|
A | T | 1 | a0001c0001t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.349+10161T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877239 | ||||||
| chr22:39877366
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.349+10034G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877366 | ||||||
| chr22:39877544
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.349+9856C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877544 | ||||||
| chr22:39877987
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.349+9413C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877987 | ||||||
| chr22:39878203
|
G | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349+9197C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878203 | ||||||
| chr22:39878444
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.349+8956G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878444 | ||||||
| chr22:39878486
|
T | TA | 11 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0023others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+8913_349+8914i others(3): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878486 | ||||||
| chr22:39878495
|
CA | C | 6 | a0001c0001t0001g0054a0001c0001t0001g0098a0001c0001t0001g0100others(3): Show | 6 | HG00738.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+8904delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878495 | ||||||
| chr22:39878799
|
A | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+8601T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878799 | ||||||
| chr22:39878916
|
T | C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.349+8484A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878916 | ||||||
| chr22:39879156
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.349+8244C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879156 | ||||||
| chr22:39879185
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0023others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+8215C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879185 | ||||||
| chr22:39879378
|
G | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.349+8022C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879378 | ||||||
| chr22:39879462
|
C | CA | 65 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0023others(62): Show | 65 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.349+7937dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879462 | ||||||
| chr22:39879462
|
C | CAA | 7 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0044others(4): Show | 7 | HG01257.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+7936_349+7937d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879462 | ||||||
| chr22:39879462
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.349+7924_349+7937d others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879462 | ||||||
| chr22:39879673
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.349+7727C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879673 | ||||||
| chr22:39879687
|
T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+7713A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879687 | ||||||
| chr22:39879694
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.349+7706C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879694 | ||||||
| chr22:39879712
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.349+7688A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879712 | ||||||
| chr22:39879713
|
T | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.349+7687A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879713 | ||||||
| chr22:39879869
|
C | T | 7 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+7531G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879869 | ||||||
| chr22:39879944
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349+7456C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879944 | ||||||
| chr22:39880504
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.349+6896C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39880504 | ||||||
| chr22:39881096
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.349+6304C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39881096 | ||||||
| chr22:39881230
|
T | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(14): Show | 18 | HG00621.hp1 HG01928.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+6170A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39881230 | ||||||
| chr22:39881244
|
A | C | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.349+6156T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39881244 | ||||||
| chr22:39882002
|
G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+5398C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882002 | ||||||
| chr22:39882094
|
A | G | 27 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.349+5306T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882094 | ||||||
| chr22:39882313
|
G | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0023a0004c0009t0001g0153 | 3 | HG02055.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.349+5087C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882313 | ||||||
| chr22:39882336
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.349+5064T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882336 | ||||||
| chr22:39882389
|
C | T | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(38): Show | 41 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.349+5011G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882389 | ||||||
| chr22:39882828
|
C | A | 2 | a0001c0001t0001g0026a0001c0001t0007g0025 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.349+4572G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882828 | ||||||
| chr22:39882945
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.349+4455T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882945 | ||||||
| chr22:39883003
|
C | CA | 8 | a0001c0001t0001g0020a0001c0001t0001g0082a0001c0001t0001g0144others(5): Show | 8 | HG00597.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.349+4396dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883003 | ||||||
| chr22:39883003
|
CA | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 44 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.349+4396delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883003 | ||||||
| chr22:39883088
|
A | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+4312T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883088 | ||||||
| chr22:39883526
|
T | C | 39 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(36): Show | 39 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.349+3874A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883526 | ||||||
| chr22:39883587
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.349+3813A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883587 | ||||||
| chr22:39883617
|
G | C | 1 | a0001c0001t0001g0148 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.349+3783C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883617 | ||||||
| chr22:39883790
|
G | C | 1 | a0001c0001t0001g0091 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.349+3610C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883790 | ||||||
| chr22:39883819
|
A | C | 4 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(1): Show | 4 | HG02083.hp1 NA18944.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+3581T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883819 | ||||||
| chr22:39883855
|
C | CA | 37 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0021others(34): Show | 37 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.349+3544dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883855 | ||||||
| chr22:39883855
|
C | CAA | 26 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 27 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.349+3543_349+3544d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883855 | ||||||
| chr22:39884029
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+3371C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884029 | ||||||
| chr22:39884059
|
AAAAG | A | 8 | a0001c0001t0001g0152a0001c0001t0001g0195a0001c0001t0001g0197others(5): Show | 8 | HG00639.hp2 HG01496.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.349+3337_349+3340d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884059 | ||||||
| chr22:39884087
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.349+3313A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884087 | ||||||
| chr22:39884372
|
G | A | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.349+3028C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884372 | ||||||
| chr22:39884380
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349+3020T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884380 | ||||||
| chr22:39884381
|
T | C | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.349+3019A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884381 | ||||||
| chr22:39884551
|
G | GA | 27 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0157others(24): Show | 27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.349+2848dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884551 | ||||||
| chr22:39885050
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0034 | 2 | NA18979.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.349+2350T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885050 | ||||||
| chr22:39885167
|
A | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.349+2233T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885167 | ||||||
| chr22:39885203
|
A | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(59): Show | 64 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.349+2197T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885203 | ||||||
| chr22:39885301
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01069.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.349+2099T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885301 | ||||||
| chr22:39885363
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.349+2037G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885363 | ||||||
| chr22:39885446
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.349+1954A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885446 | ||||||
| chr22:39885671
|
T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+1729A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885671 | ||||||
| chr22:39885691
|
C | T | 40 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(37): Show | 40 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.349+1709G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885691 | ||||||
| chr22:39886058
|
GT | G | 40 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(37): Show | 40 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.349+1341delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886058 | ||||||
| chr22:39886070
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+1330T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886070 | ||||||
| chr22:39886095
|
T | C | 5 | a0001c0001t0001g0188a0001c0001t0003g0004a0001c0003t0001g0006others(2): Show | 5 | HG02622.hp2 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+1305A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886095 | ||||||
| chr22:39886292
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.349+1108T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886292 | ||||||
| chr22:39886667
|
T | C | 1 | a0001c0001t0002g0172 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.349+733A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886667 | ||||||
| chr22:39886680
|
AGAGAGGA others(6): Show |
A | 1 | a0001c0001t0001g0112 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.349+707_349+719del others(13): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886680 | ||||||
| chr22:39887181
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.349+219A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39887181 | ||||||
| chr22:39888194
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-155-291C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888194 | ||||||
| chr22:39888260
|
C | CT | 18 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 19 | HG00621.hp1 HG01928.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.-155-358dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | ||||||
| chr22:39888260
|
CT | C | 77 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0023others(74): Show | 77 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.-155-358delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | ||||||
| chr22:39888260
|
CTT | C | 11 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0121others(8): Show | 11 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-155-359_-155-358d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | ||||||
| chr22:39888260
|
CTTTTTTT | C | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG00735.hp1 HG01069.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-155-364_-155-358d others(9): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | ||||||
| chr22:39888260
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-155-367_-155-358d others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | ||||||
| chr22:39888264
|
T | C | 4 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 4 | HG00140.hp1 HG01070.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-155-361A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888264 | ||||||
| chr22:39888516
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0001g0195a0001c0001t0001g0199others(2): Show | 5 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-155-613G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888516 | ||||||
| chr22:39888519
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-155-616G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888519 | ||||||
| chr22:39888535
|
A | C | 34 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0051others(31): Show | 34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-155-632T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888535 | ||||||
| chr22:39888722
|
G | A | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-155-819C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888722 | ||||||
| chr22:39888865
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-155-962A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888865 | ||||||
| chr22:39888866
|
C | A | 2 | a0001c0004t0001g0093a0001c0004t0001g0094 | 2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-155-963G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888866 | ||||||
| chr22:39889670
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-155-1767T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889670 | ||||||
| chr22:39889734
|
T | A | 5 | a0002c0002t0001g0176a0002c0002t0001g0190a0002c0002t0001g0191others(2): Show | 5 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-155-1831A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889734 | ||||||
| chr22:39889735
|
A | T | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0005c0007t0001g0125 | 3 | NA18977.hp1 NA19000.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-155-1832T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889735 | ||||||
| chr22:39889767
|
T | C | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-155-1864A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889767 | ||||||
| chr22:39889868
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-155-1965C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889868 | ||||||
| chr22:39890016
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 171 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.-155-2113C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890016 | ||||||
| chr22:39890099
|
A | AAAAT | 9 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0048others(6): Show | 9 | HG01069.hp1 HG02148.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-155-2200_-155-219 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | ||||||
| chr22:39890099
|
AAAAT | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(93): Show | 97 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-155-2200_-155-219 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | ||||||
| chr22:39890099
|
AAAATAAA others(1): Show |
A | 46 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(43): Show | 46 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.-155-2204_-155-219 others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | ||||||
| chr22:39890099
|
AAAATAAA others(5): Show |
A | 2 | a0001c0001t0001g0150a0001c0001t0001g0175 | 2 | HG02523.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-155-2208_-155-219 others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | ||||||
| chr22:39890099
|
AAAATAAA others(9): Show |
A | 2 | a0001c0001t0001g0122a0001c0001t0001g0194 | 2 | HG01192.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-155-2212_-155-219 others(20): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | ||||||
| chr22:39890099
|
AAAATAAA others(21): Show |
A | 1 | a0001c0001t0001g0151 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-155-2224_-155-219 others(32): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | ||||||
| chr22:39890143
|
TAAATAAA others(1): Show |
T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | NA18967.hp2 NA18983.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-155-2248_-155-224 others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890143 | ||||||
| chr22:39890266
|
G | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 36 | HG00438.hp1 HG00597.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.-155-2363C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890266 | ||||||
| chr22:39890363
|
GT | G | 8 | a0001c0001t0001g0152a0001c0001t0001g0195a0001c0001t0001g0197others(5): Show | 8 | HG00639.hp2 HG01496.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-155-2461delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890363 | ||||||
| chr22:39890381
|
CT | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0023a0004c0009t0001g0153 | 3 | HG02055.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-155-2479delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890381 | ||||||
| chr22:39890751
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(19): Show | 23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.-155-2848G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890751 | ||||||
| chr22:39891366
|
A | G | 1 | a0002c0002t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-156+2329T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891366 | ||||||
| chr22:39891475
|
C | CT | 11 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0043others(8): Show | 11 | HG01891.hp1 HG02145.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-156+2219dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891475 | ||||||
| chr22:39891475
|
C | CTT | 23 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.-156+2218_-156+221 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891475 | ||||||
| chr22:39891620
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-156+2075T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891620 | ||||||
| chr22:39891621
|
T | A | 28 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0002g0156others(25): Show | 28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-156+2074A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891621 | ||||||
| chr22:39891645
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-156+2050C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891645 | ||||||
| chr22:39891808
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-156+1887G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891808 | ||||||
| chr22:39891909
|
C | G | 1 | a0006c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-156+1786G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891909 | ||||||
| chr22:39891930
|
T | A | 3 | a0001c0001t0001g0173a0002c0002t0001g0210a0002c0002t0001g0211 | 3 | HG00642.hp2 HG01168.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-156+1765A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891930 | ||||||
| chr22:39891973
|
A | G | 1 | a0001c0001t0001g0018 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-156+1722T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891973 | ||||||
| chr22:39892243
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-156+1452T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892243 | ||||||
| chr22:39892381
|
T | C | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(42): Show | 45 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-156+1314A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892381 | ||||||
| chr22:39892614
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-156+1081A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892614 | ||||||
| chr22:39892648
|
C | T | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-156+1047G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892648 | ||||||
| chr22:39892668
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1027C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892668 | ||||||
| chr22:39892669
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1026C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892669 | ||||||
| chr22:39892670
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1025C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892670 | ||||||
| chr22:39892671
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1024T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892671 | ||||||
| chr22:39892675
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1020A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892675 | ||||||
| chr22:39892676
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1019T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892676 | ||||||
| chr22:39892749
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-156+946C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892749 | ||||||
| chr22:39892826
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG03017.hp2 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-156+869T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892826 | ||||||
| chr22:39893456
|
G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-156+239C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893456 | ||||||
| chr22:39893507
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-156+188T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893507 | ||||||
| chr22:39893588
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-156+107G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893588 | ||||||
| chr22:39893604
|
C | T | 3 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0008 | 3 | HG02622.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-156+91G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893604 | ||||||
| chr22:39893623
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-156+72C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893623 |