Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 58478 |
| ensemblid | ENSG00000145293.17 |
| hgncid | 24599 |
| symbol | ENOPH1 |
| name | enolase-phosphatase 1 |
| refseq_nuc | NM_021204.5 |
| refseq_prot | NP_067027.1 |
| ensembl_nuc | ENST00000273920.8 |
| ensembl_prot | ENSP00000273920.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 82430590 |
| end | 82461177 |
| strand | + |
| ver | v1.2 |
| region | chr4:82430590-82461177 |
| region5000 | chr4:82425590-82466177 |
| regionname0 | ENOPH1_chr4_82430590_82461177 |
| regionname5000 | ENOPH1_chr4_82425590_82466177 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 261 | 364 | 95 | 63 | 154 | 12 | 38 | 120 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | MVVLS others(256): Show |
chr4 | 82425590 | 82466177 |
| a0002 | 0/0 | 261 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | MVVLS others(256): Show |
chr4 | 82425590 | 82466177 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 783 | 363 | 95 | 63 | 153 | 12 | 38 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | ATGGT others(778): Show |
chr4 | 82425590 | 82466177 | ||
| a0001c0003 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | ATGGT others(778): Show |
chr4 | 82425590 | 82466177 | ||
| a0002c0002 | 0/0 | 783 | 2 | 1 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | ATGGT others(778): Show |
chr4 | 82425590 | 82466177 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2083 | 256 | 56 | 52 | 107 | 10 | 29 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0001t0002 | 0/0 | 2083 | 28 | 4 | 3 | 13 | 1 | 7 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0001t0003 | 0/0 | 2083 | 22 | 1 | 2 | 19 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0001t0004 | 0/0 | 2083 | 21 | 14 | 0 | 7 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0001t0005 | 0/0 | 2083 | 12 | 0 | 6 | 5 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0001t0006 | 0/0 | 2083 | 11 | 11 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0001t0007 | 0/0 | 2083 | 9 | 9 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0001t0008 | 0/0 | 2083 | 2 | 0 | 0 | 0 | 0 | 2 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0001t0009 | 0/0 | 2083 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0001t0010 | 0/0 | 2083 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0001c0003t0005 | 0/0 | 2083 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| a0002c0002t0001 | 0/0 | 2083 | 2 | 1 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | GTCTC others(2078): Show |
chr4 | 82425590 | 82466177 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 3 | 0 | 3 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0032 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0019 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0007g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0001c0003t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | GBR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | GBR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | FIN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0283 | EUR | FIN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | CHS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0088 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0147 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0089 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0093 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0286 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | KHV | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0090 | AMR | PEL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | CDX | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | CDX | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0071 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0110 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0063 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0264 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0070 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0067 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03491 | hp2 | a0001 | c0001 | t0008 | g0001 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0001 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18975 | hp2 | a0001 | c0003 | t0005 | g0103 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19066 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | YRI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ASW | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0097 | EUR | TSI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | TSI | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0075 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | ACB | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0076 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | USA | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0109 | AFR | LWK | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0032 | REF | REF | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0064 | REF | REF | ENOPH1_chr4_82425590_82466177 | ENOPH1 | chr4 | 82425590 | 82466177 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82451233 | G | A | 1 | a0002 | 2 | HG01256.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.377G>A | p.Arg126His | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/6 | 617/2083 | 377/786 | 126/261 | chr4 | 82451233 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82460042 | A | G | 1 | a0001c0003 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.708A>G | p.Ala236Ala | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 948/2083 | 708/786 | 236/261 | chr4 | 82460042 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82430668 | A | G | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(2): Show |
61 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-162A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/6 | 162 | chr4 | 82430668 | ||||||
| chr4:82430692 | G | T | 3 | a0001c0001t0002 a0001c0001t0005 a0001c0003t0005 |
41 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(38): Show |
5_prime_UTR_variant | MODIFIER | c.-138G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/6 | 138 | chr4 | 82430692 | ||||||
| chr4:82460142 | C | T | 2 | a0001c0001t0004 a0001c0001t0006 |
32 | HG01891.hp1 HG02132.hp2 HG02145.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*22C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 22 | chr4 | 82460142 | ||||||
| chr4:82460411 | C | A | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0003t0005 |
35 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*291C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 291 | chr4 | 82460411 | ||||||
| chr4:82460746 | T | C | 1 | a0001c0001t0009 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*626T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 626 | chr4 | 82460746 | ||||||
| chr4:82460851 | A | G | 1 | a0001c0001t0010 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 731 | chr4 | 82460851 | ||||||
| chr4:82461126 | C | T | 1 | a0001c0001t0008 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1006C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 6/6 | 1006 | chr4 | 82461126 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:82430996 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.84+83G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82430996 | |||||||
| chr4:82430997 | A | C | 1 | a0001c0001t0001g0293 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.84+84A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82430997 | |||||||
| chr4:82431024 | C | CTT | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(267): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.84+112_84+113insTT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82431024 | ||||||
| chr4:82431033 | G | C | 50 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(47): Show |
55 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.84+120G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431033 | |||||||
| chr4:82431203 | G | T | 1 | a0001c0001t0001g0292 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.84+290G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431203 | |||||||
| chr4:82431302 | C | T | 2 | a0001c0001t0004g0290 a0001c0001t0004g0291 |
2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.84+389C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431302 | |||||||
| chr4:82431305 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.84+392C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431305 | |||||||
| chr4:82431617 | G | T | 3 | a0001c0001t0006g0109 a0001c0001t0006g0110 a0001c0001t0006g0111 |
3 | HG02559.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.84+704G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431617 | |||||||
| chr4:82431704 | T | A | 14 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(11): Show |
15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+791T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431704 | |||||||
| chr4:82431834 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.84+921C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431834 | |||||||
| chr4:82431891 | A | T | 15 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(12): Show |
16 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.84+978A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431891 | |||||||
| chr4:82431915 | C | CT | 9 | a0001c0001t0001g0066 a0001c0001t0001g0281 a0001c0001t0001g0282 others(6): Show |
9 | HG00323.hp2 HG01192.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+1016dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82431915 | ||||||
| chr4:82431915 | CT | C | 39 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0002g0019 others(36): Show |
43 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.84+1016delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82431915 | ||||||
| chr4:82431948 | G | C | 2 | a0001c0001t0004g0044 a0001c0001t0004g0045 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.84+1035G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82431948 | |||||||
| chr4:82432017 | A | G | 37 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(34): Show |
41 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.84+1104A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432017 | |||||||
| chr4:82432644 | C | CGTTTT | 10 | a0001c0001t0001g0013 a0001c0001t0001g0285 a0001c0001t0002g0079 others(7): Show |
13 | HG01884.hp2 HG02717.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+1756_84+1760dup others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432644 | ||||||
| chr4:82432644 | C | CGTTTTGT others(3): Show |
7 | a0001c0001t0001g0279 a0001c0001t0006g0071 a0001c0001t0006g0072 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+1751_84+1760dup others(10): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432644 | ||||||
| chr4:82432644 | C | CGTTTTGT others(8): Show |
4 | a0001c0001t0001g0280 a0001c0001t0002g0080 a0001c0001t0002g0107 others(1): Show |
4 | HG00621.hp1 HG03491.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+1746_84+1760dup others(15): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432644 | ||||||
| chr4:82432644 | C | CGTTTTGT others(13): Show |
30 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0081 others(27): Show |
34 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.84+1741_84+1760dup others(20): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432644 | ||||||
| chr4:82432688 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG03225.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.84+1775T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432688 | |||||||
| chr4:82432791 | C | A | 13 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(10): Show |
13 | HG02572.hp1 HG02615.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+1878C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432791 | |||||||
| chr4:82432805 | A | G | 5 | a0001c0001t0007g0016 a0001c0001t0007g0067 a0001c0001t0007g0068 others(2): Show |
6 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+1892A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432805 | |||||||
| chr4:82432901 | C | T | 1 | a0001c0001t0006g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.84+1988C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82432901 | |||||||
| chr4:82432985 | CT | C | 50 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(47): Show |
55 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.84+2081delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82432985 | ||||||
| chr4:82433247 | C | G | 1 | a0001c0001t0001g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.84+2334C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433247 | |||||||
| chr4:82433307 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.84+2394G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433307 | |||||||
| chr4:82433361 | T | C | 14 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(11): Show |
15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+2448T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433361 | |||||||
| chr4:82433388 | T | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+2475T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433388 | |||||||
| chr4:82433513 | A | G | 2 | a0001c0001t0003g0042 a0001c0001t0003g0277 |
3 | NA18991.hp1 NA19004.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.84+2600A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433513 | |||||||
| chr4:82433682 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.84+2769A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433682 | |||||||
| chr4:82433742 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.84+2829C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433742 | |||||||
| chr4:82433803 | T | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+2890T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433803 | |||||||
| chr4:82433868 | T | C | 34 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0112 others(31): Show |
36 | HG00558.hp2 HG00597.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+2955T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82433868 | |||||||
| chr4:82434185 | G | A | 2 | a0001c0001t0004g0290 a0001c0001t0004g0291 |
2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.84+3272G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434185 | |||||||
| chr4:82434348 | C | T | 2 | a0001c0001t0004g0161 a0001c0001t0004g0162 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.84+3435C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434348 | |||||||
| chr4:82434474 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
113 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.84+3561G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434474 | |||||||
| chr4:82434479 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.84+3566C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434479 | |||||||
| chr4:82434543 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.84+3630G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434543 | |||||||
| chr4:82434571 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.84+3658G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434571 | |||||||
| chr4:82434721 | G | A | 50 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(47): Show |
55 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.84+3808G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434721 | |||||||
| chr4:82434769 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.84+3856T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434769 | |||||||
| chr4:82434776 | G | A | 32 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(29): Show |
36 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+3863G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434776 | |||||||
| chr4:82434822 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.84+3909G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434822 | |||||||
| chr4:82434897 | A | ACT | 50 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(47): Show |
55 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.84+3985_84+3986dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82434897 | ||||||
| chr4:82434898 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+3985C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82434898 | |||||||
| chr4:82434905 | TA | T | 7 | a0001c0001t0001g0131 a0001c0001t0001g0160 a0001c0001t0001g0225 others(4): Show |
7 | HG01168.hp2 HG02040.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+4006delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82434905 | ||||||
| chr4:82435054 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
8 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+4141C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435054 | |||||||
| chr4:82435197 | G | A | 1 | a0001c0001t0003g0163 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.84+4284G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435197 | |||||||
| chr4:82435294 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.84+4381G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435294 | |||||||
| chr4:82435445 | G | A | 14 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(11): Show |
15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+4532G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435445 | |||||||
| chr4:82435535 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.84+4622A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435535 | |||||||
| chr4:82435741 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0003g0274 |
2 | NA18977.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.84+4828A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435741 | |||||||
| chr4:82435836 | A | G | 14 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(11): Show |
15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+4923A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435836 | |||||||
| chr4:82435846 | A | G | 14 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(11): Show |
15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+4933A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435846 | |||||||
| chr4:82435940 | T | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
96 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.84+5027T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435940 | |||||||
| chr4:82435944 | A | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+5031A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435944 | |||||||
| chr4:82435967 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0228 |
2 | NA18982.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.84+5054C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435967 | |||||||
| chr4:82435999 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.84+5086T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82435999 | |||||||
| chr4:82436163 | C | T | 32 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(29): Show |
36 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+5250C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436163 | |||||||
| chr4:82436300 | C | T | 1 | a0001c0001t0003g0277 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.84+5387C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436300 | |||||||
| chr4:82436392 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.84+5479G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436392 | |||||||
| chr4:82436483 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.84+5570C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436483 | |||||||
| chr4:82436641 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.84+5728C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436641 | |||||||
| chr4:82436686 | C | CA | 33 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(30): Show |
39 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.84+5791dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82436686 | ||||||
| chr4:82436686 | C | CAA | 9 | a0001c0001t0004g0044 a0001c0001t0006g0072 a0001c0001t0006g0073 others(6): Show |
9 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+5790_84+5791dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82436686 | ||||||
| chr4:82436686 | C | CAAA | 6 | a0001c0001t0006g0071 a0001c0001t0007g0016 a0001c0001t0007g0067 others(3): Show |
7 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+5789_84+5791dup others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82436686 | ||||||
| chr4:82436686 | CA | C | 34 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0002g0019 others(31): Show |
38 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.84+5791delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82436686 | ||||||
| chr4:82436840 | AGTTCCCT others(5): Show |
A | 1 | a0001c0001t0001g0275 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.84+5928_84+5939del others(12): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82436840 | |||||||
| chr4:82437251 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0225 others(1): Show |
4 | HG02080.hp2 NA18990.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+6338G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437251 | |||||||
| chr4:82437512 | G | A | 1 | a0001c0001t0006g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.84+6599G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437512 | |||||||
| chr4:82437535 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.84+6622A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437535 | |||||||
| chr4:82437609 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(25): Show |
34 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.84+6696T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437609 | |||||||
| chr4:82437652 | G | A | 3 | a0001c0001t0006g0109 a0001c0001t0006g0110 a0001c0001t0006g0111 |
3 | HG02559.hp2 HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.84+6739G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437652 | |||||||
| chr4:82437826 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.84+6913A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437826 | |||||||
| chr4:82437831 | G | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0271 a0001c0001t0001g0272 |
7 | HG00099.hp1 HG00738.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.84+6918G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437831 | |||||||
| chr4:82437884 | C | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.84+6971C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82437884 | |||||||
| chr4:82438035 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.84+7122T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438035 | |||||||
| chr4:82438158 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.84+7245C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438158 | |||||||
| chr4:82438221 | G | A | 2 | a0001c0001t0007g0067 a0001c0001t0007g0068 |
2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.84+7308G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438221 | |||||||
| chr4:82438391 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.84+7478C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438391 | |||||||
| chr4:82438420 | A | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(70): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.84+7507A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438420 | |||||||
| chr4:82438431 | AT | A | 32 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(29): Show |
36 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+7520delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82438431 | ||||||
| chr4:82438503 | A | T | 1 | a0001c0001t0001g0275 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.84+7590A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438503 | |||||||
| chr4:82438505 | T | G | 1 | a0001c0001t0001g0275 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.84+7592T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438505 | |||||||
| chr4:82438676 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0215 a0001c0001t0004g0159 |
3 | HG01123.hp2 HG02027.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.84+7763A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438676 | |||||||
| chr4:82438880 | T | C | 32 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(29): Show |
36 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+7967T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438880 | |||||||
| chr4:82438892 | C | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.84+7979C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438892 | |||||||
| chr4:82438999 | C | T | 14 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(11): Show |
15 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.84+8086C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82438999 | |||||||
| chr4:82439033 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.84+8120A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439033 | |||||||
| chr4:82439051 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0004g0159 |
2 | HG01123.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.84+8138C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439051 | |||||||
| chr4:82439054 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.84+8141G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439054 | |||||||
| chr4:82439086 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG00323.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.84+8173C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439086 | |||||||
| chr4:82439305 | C | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.84+8392C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439305 | |||||||
| chr4:82439631 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
6 | HG01167.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-8289A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439631 | |||||||
| chr4:82439785 | T | C | 2 | a0001c0001t0006g0021 a0001c0001t0007g0286 |
3 | HG02055.hp1 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.85-8135T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439785 | |||||||
| chr4:82439892 | G | C | 1 | a0001c0001t0001g0024 | 2 | NA18941.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.85-8028G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82439892 | |||||||
| chr4:82440430 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.85-7490G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440430 | |||||||
| chr4:82440477 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.85-7443C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440477 | |||||||
| chr4:82440762 | ATAATT | A | 5 | a0001c0001t0007g0016 a0001c0001t0007g0067 a0001c0001t0007g0068 others(2): Show |
6 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-7153_85-7149del others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82440762 | ||||||
| chr4:82440784 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.85-7136G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440784 | |||||||
| chr4:82440980 | A | G | 14 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(11): Show |
14 | HG02258.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.85-6940A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440980 | |||||||
| chr4:82440984 | A | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.85-6936A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82440984 | |||||||
| chr4:82441039 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(81): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.85-6881A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441039 | |||||||
| chr4:82441091 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.85-6829G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441091 | |||||||
| chr4:82441210 | C | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0033 others(26): Show |
35 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.85-6710C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441210 | |||||||
| chr4:82441303 | C | T | 5 | a0001c0001t0004g0290 a0001c0001t0004g0291 a0001c0001t0006g0109 others(2): Show |
5 | HG02559.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-6617C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441303 | |||||||
| chr4:82441360 | T | C | 6 | a0001c0001t0001g0140 a0001c0001t0001g0282 a0001c0001t0004g0138 others(3): Show |
6 | HG02132.hp2 HG02165.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-6560T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441360 | |||||||
| chr4:82441371 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.85-6549C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441371 | |||||||
| chr4:82441405 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.85-6515G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441405 | |||||||
| chr4:82441431 | T | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0232 a0001c0001t0001g0236 |
3 | HG01891.hp2 HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.85-6489T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441431 | |||||||
| chr4:82441432 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0232 a0001c0001t0001g0236 |
3 | HG01891.hp2 HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.85-6488T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441432 | |||||||
| chr4:82441549 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.85-6371A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441549 | |||||||
| chr4:82441591 | G | A | 1 | a0001c0001t0003g0168 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.85-6329G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441591 | |||||||
| chr4:82441637 | A | G | 30 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(27): Show |
36 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.85-6283A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441637 | |||||||
| chr4:82441653 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.85-6267T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441653 | |||||||
| chr4:82441715 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.85-6205G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441715 | |||||||
| chr4:82441764 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.85-6156A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441764 | |||||||
| chr4:82441776 | AAAAC | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0025 others(19): Show |
26 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.85-6141_85-6138del others(4): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82441776 | ||||||
| chr4:82441777 | A | AAAC | 6 | a0001c0001t0001g0040 a0001c0001t0001g0158 a0001c0001t0001g0230 others(3): Show |
6 | HG00140.hp1 HG01123.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-6125_85-6123dup others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82441777 | ||||||
| chr4:82441801 | T | C | 2 | a0001c0001t0005g0017 a0001c0001t0005g0083 |
3 | HG00609.hp1 NA18960.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.85-6119T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441801 | |||||||
| chr4:82441922 | T | A | 6 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-5998T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82441922 | |||||||
| chr4:82442137 | T | G | 4 | a0001c0001t0002g0080 a0001c0001t0002g0084 a0001c0001t0002g0086 others(1): Show |
4 | HG00438.hp2 HG00621.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-5783T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442137 | |||||||
| chr4:82442184 | A | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(25): Show |
33 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.85-5736A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442184 | |||||||
| chr4:82442268 | C | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(28): Show |
36 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.85-5652C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442268 | |||||||
| chr4:82442306 | G | C | 6 | a0001c0001t0001g0135 a0001c0001t0001g0143 a0001c0001t0004g0144 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-5614G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442306 | |||||||
| chr4:82442420 | C | T | 33 | a0001c0001t0001g0155 a0001c0001t0001g0270 a0001c0001t0002g0019 others(30): Show |
37 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-5500C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442420 | |||||||
| chr4:82442475 | G | A | 7 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0007g0016 others(4): Show |
8 | HG00323.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-5445G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442475 | |||||||
| chr4:82442531 | CAA | C | 8 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0006g0071 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-5382_85-5381del others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82442531 | ||||||
| chr4:82442547 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0062 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-5373G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442547 | |||||||
| chr4:82442558 | A | AT | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
14 | HG02572.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.85-5352dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82442558 | ||||||
| chr4:82442558 | AT | A | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-5352delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82442558 | ||||||
| chr4:82442629 | A | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(22): Show |
30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-5291A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442629 | |||||||
| chr4:82442734 | C | T | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
14 | HG02572.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.85-5186C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442734 | |||||||
| chr4:82442864 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
8 | HG02083.hp2 NA18945.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-5056G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442864 | |||||||
| chr4:82442931 | T | TCTCATGT others(3): Show |
1 | a0001c0001t0001g0237 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.85-4988_85-4979dup others(10): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82442931 | ||||||
| chr4:82442998 | G | T | 31 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0061 others(28): Show |
33 | HG00323.hp2 HG01167.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.85-4922G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82442998 | |||||||
| chr4:82443071 | G | A | 2 | a0001c0001t0004g0044 a0001c0001t0004g0045 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.85-4849G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443071 | |||||||
| chr4:82443094 | C | T | 1 | a0001c0001t0006g0111 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85-4826C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443094 | |||||||
| chr4:82443100 | C | T | 2 | a0001c0001t0004g0161 a0001c0001t0004g0162 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.85-4820C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443100 | |||||||
| chr4:82443243 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.85-4677C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443243 | |||||||
| chr4:82443369 | C | T | 1 | a0001c0001t0006g0110 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.85-4551C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443369 | |||||||
| chr4:82443410 | C | CA | 30 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0119 others(27): Show |
32 | HG00323.hp2 HG01167.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.85-4500dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443410 | ||||||
| chr4:82443525 | G | A | 1 | a0001c0001t0004g0138 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.85-4395G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443525 | |||||||
| chr4:82443528 | G | A | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4392G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443528 | |||||||
| chr4:82443538 | T | C | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4382T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443538 | |||||||
| chr4:82443544 | T | C | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4376T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443544 | |||||||
| chr4:82443570 | C | T | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4350C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443570 | |||||||
| chr4:82443581 | G | A | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4339G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443581 | |||||||
| chr4:82443588 | C | T | 6 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-4332C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443588 | |||||||
| chr4:82443594 | G | A | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4326G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443594 | |||||||
| chr4:82443596 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.85-4324C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443596 | |||||||
| chr4:82443606 | A | T | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4314A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443606 | |||||||
| chr4:82443618 | C | T | 1 | a0001c0001t0006g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.85-4302C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443618 | |||||||
| chr4:82443638 | A | G | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4282A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443638 | |||||||
| chr4:82443645 | A | G | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4275A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443645 | |||||||
| chr4:82443653 | A | G | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4267A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443653 | |||||||
| chr4:82443655 | C | G | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4265C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443655 | |||||||
| chr4:82443659 | T | C | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4261T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443659 | |||||||
| chr4:82443676 | T | C | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4244T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443676 | |||||||
| chr4:82443682 | T | C | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4238T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443682 | |||||||
| chr4:82443684 | T | C | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4236T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443684 | |||||||
| chr4:82443693 | C | A | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4227C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443693 | |||||||
| chr4:82443704 | G | GGC | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4215_85-4214ins others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443704 | ||||||
| chr4:82443712 | T | C | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4208T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443712 | |||||||
| chr4:82443718 | T | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0133 others(4): Show |
7 | HG01167.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-4202T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443718 | |||||||
| chr4:82443720 | CA | C | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-4199delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443720 | |||||||
| chr4:82443726 | C | CAAAAAAA others(7): Show |
24 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(21): Show |
27 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.85-4184_85-4183ins others(14): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443726 | ||||||
| chr4:82443726 | C | CAAAAAAA others(8): Show |
9 | a0001c0001t0002g0081 a0001c0001t0002g0091 a0001c0001t0002g0092 others(6): Show |
10 | HG01109.hp2 HG01175.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.85-4184_85-4183ins others(15): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443726 | ||||||
| chr4:82443771 | GTTTAA | G | 6 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(3): Show |
6 | NA18939.hp1 NA18939.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-4145_85-4141del others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82443771 | ||||||
| chr4:82443827 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.85-4093T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82443827 | |||||||
| chr4:82444007 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85-3913C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444007 | |||||||
| chr4:82444225 | C | CT | 43 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(40): Show |
47 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.85-3681dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82444225 | ||||||
| chr4:82444243 | A | G | 7 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0007g0016 others(4): Show |
8 | HG00323.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-3677A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444243 | |||||||
| chr4:82444335 | T | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(96): Show |
111 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.85-3585T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444335 | |||||||
| chr4:82444438 | C | T | 23 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0119 others(20): Show |
24 | HG01167.hp2 HG02055.hp1 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.85-3482C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444438 | |||||||
| chr4:82444447 | A | G | 9 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(6): Show |
9 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-3473A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444447 | |||||||
| chr4:82444501 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(63): Show |
75 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.85-3419C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444501 | |||||||
| chr4:82444563 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.85-3357G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444563 | |||||||
| chr4:82444602 | G | C | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-3318G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444602 | |||||||
| chr4:82444645 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85-3275A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444645 | |||||||
| chr4:82444833 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0269 |
6 | HG01255.hp2 HG01346.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-3087A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82444833 | |||||||
| chr4:82445155 | G | T | 7 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0007g0016 others(4): Show |
8 | HG00323.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-2765G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445155 | |||||||
| chr4:82445215 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.85-2705C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445215 | |||||||
| chr4:82445235 | GA | G | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-2675delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82445235 | ||||||
| chr4:82445307 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.85-2613T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445307 | |||||||
| chr4:82445485 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(63): Show |
75 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.85-2435C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445485 | |||||||
| chr4:82445520 | A | G | 1 | a0001c0001t0007g0069 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.85-2400A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445520 | |||||||
| chr4:82445678 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.85-2242A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445678 | |||||||
| chr4:82445876 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0273 |
2 | HG00408.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.85-2044A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445876 | |||||||
| chr4:82445930 | C | T | 41 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(38): Show |
45 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.85-1990C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82445930 | |||||||
| chr4:82446156 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(22): Show |
30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1764G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446156 | |||||||
| chr4:82446190 | G | A | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-1730G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446190 | |||||||
| chr4:82446413 | C | T | 9 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(6): Show |
9 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-1507C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446413 | |||||||
| chr4:82446421 | C | CA | 50 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(47): Show |
54 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.85-1487dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446421 | ||||||
| chr4:82446421 | C | CAA | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(22): Show |
30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1488_85-1487dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446421 | ||||||
| chr4:82446467 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.85-1453C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446467 | |||||||
| chr4:82446662 | C | CT | 69 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0119 others(66): Show |
74 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.85-1244dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446662 | ||||||
| chr4:82446662 | C | CTT | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(22): Show |
30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1245_85-1244dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446662 | ||||||
| chr4:82446673 | T | G | 4 | a0001c0001t0001g0215 a0001c0001t0001g0282 a0001c0001t0003g0042 others(1): Show |
5 | HG02027.hp2 NA18954.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.85-1247T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446673 | |||||||
| chr4:82446675 | T | G | 20 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(17): Show |
25 | HG00438.hp1 HG00735.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.85-1245T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446675 | |||||||
| chr4:82446676 | TG | T | 30 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0135 others(27): Show |
32 | HG00140.hp2 HG00597.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.85-1243delG | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446676 | |||||||
| chr4:82446677 | G | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.85-1243G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446677 | |||||||
| chr4:82446683 | C | G | 1 | a0001c0001t0004g0157 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.85-1237C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446683 | |||||||
| chr4:82446689 | C | CT | 68 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(65): Show |
82 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.85-1203dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | ||||||
| chr4:82446689 | CT | C | 11 | a0001c0001t0001g0289 a0001c0001t0002g0079 a0001c0001t0002g0080 others(8): Show |
11 | HG00438.hp2 HG00621.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-1203delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | ||||||
| chr4:82446689 | CTT | C | 22 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0082 others(19): Show |
26 | HG00558.hp1 HG00609.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.85-1204_85-1203del others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | ||||||
| chr4:82446689 | CTTTTTTT others(1): Show |
C | 29 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0119 others(26): Show |
31 | HG00323.hp2 HG01167.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.85-1210_85-1203del others(8): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | ||||||
| chr4:82446689 | CTTTTTTT others(7): Show |
C | 8 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0006g0071 others(5): Show |
8 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-1216_85-1203del others(14): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | ||||||
| chr4:82446689 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0057 |
3 | HG02809.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.85-1217_85-1203del others(15): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | ||||||
| chr4:82446689 | CTTTTTTT others(9): Show |
C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(20): Show |
27 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.85-1218_85-1203del others(16): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82446689 | ||||||
| chr4:82446721 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.85-1199A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446721 | |||||||
| chr4:82446722 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.85-1198C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446722 | |||||||
| chr4:82446747 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.85-1173C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446747 | |||||||
| chr4:82446778 | C | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(22): Show |
30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1142C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446778 | |||||||
| chr4:82446792 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.85-1128C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446792 | |||||||
| chr4:82446831 | C | T | 1 | a0001c0001t0005g0085 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.85-1089C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446831 | |||||||
| chr4:82446852 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.85-1068G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446852 | |||||||
| chr4:82446861 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(22): Show |
30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-1059C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446861 | |||||||
| chr4:82446868 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0253 |
3 | HG02896.hp2 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.85-1052G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446868 | |||||||
| chr4:82446875 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0253 |
3 | HG02896.hp2 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.85-1045T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446875 | |||||||
| chr4:82446928 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(22): Show |
30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-992G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446928 | |||||||
| chr4:82446969 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.85-951G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82446969 | |||||||
| chr4:82447237 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.85-683C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447237 | |||||||
| chr4:82447335 | A | G | 1 | a0001c0001t0007g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.85-585A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447335 | |||||||
| chr4:82447353 | GTTTGT | G | 7 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0133 others(4): Show |
7 | HG01167.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-558_85-554delGT others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 82447353 | ||||||
| chr4:82447464 | G | A | 33 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(30): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.85-456G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447464 | |||||||
| chr4:82447573 | C | T | 6 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-347C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447573 | |||||||
| chr4:82447827 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(22): Show |
30 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.85-93T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 1/5 | chr4 | 82447827 | |||||||
| chr4:82448134 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.186+113A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448134 | |||||||
| chr4:82448223 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.186+202T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448223 | |||||||
| chr4:82448236 | G | GT | 5 | a0001c0001t0001g0164 a0001c0001t0007g0016 a0001c0001t0007g0067 others(2): Show |
6 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+224dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82448236 | ||||||
| chr4:82448241 | TTTTTGTT others(3): Show |
T | 1 | a0001c0003t0005g0103 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.186+235_186+244del others(10): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82448241 | ||||||
| chr4:82448251 | GTTTTGTT others(7): Show |
G | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0002c0002t0001g0169 |
3 | HG00323.hp2 HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.186+240_186+253del others(14): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82448251 | ||||||
| chr4:82448260 | TG | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0056 |
7 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+240delG | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448260 | |||||||
| chr4:82448266 | T | G | 1 | a0002c0002t0001g0147 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.186+245T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448266 | |||||||
| chr4:82448270 | G | GT | 17 | a0001c0001t0001g0040 a0001c0001t0001g0132 a0001c0001t0001g0158 others(14): Show |
18 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.186+258dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82448270 | ||||||
| chr4:82448271 | T | G | 9 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(6): Show |
9 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.186+250T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448271 | |||||||
| chr4:82448346 | C | A | 6 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+325C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448346 | |||||||
| chr4:82448507 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.186+486C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448507 | |||||||
| chr4:82448545 | A | C | 3 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0063 |
3 | HG02895.hp1 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.186+524A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448545 | |||||||
| chr4:82448715 | A | G | 41 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0079 others(38): Show |
45 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.186+694A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448715 | |||||||
| chr4:82448728 | C | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(20): Show |
27 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.186+707C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448728 | |||||||
| chr4:82448860 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.186+839C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448860 | |||||||
| chr4:82448864 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.186+843T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82448864 | |||||||
| chr4:82449057 | C | CA | 9 | a0001c0001t0001g0223 a0001c0001t0002g0079 a0001c0001t0002g0080 others(6): Show |
9 | HG00621.hp1 HG01175.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+1060dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | ||||||
| chr4:82449057 | CA | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.186+1060delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | ||||||
| chr4:82449057 | CAA | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(66): Show |
75 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.186+1059_186+1060d others(4): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | ||||||
| chr4:82449057 | CAAA | C | 22 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0061 others(19): Show |
25 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.186+1058_186+1060d others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | ||||||
| chr4:82449057 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0057 |
3 | HG02809.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.186+1051_186+1060d others(12): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 82449057 | ||||||
| chr4:82449189 | G | A | 16 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0119 others(13): Show |
16 | HG01167.hp2 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.186+1168G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449189 | |||||||
| chr4:82449212 | C | T | 7 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0007g0016 others(4): Show |
8 | HG00323.hp2 HG01192.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+1191C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449212 | |||||||
| chr4:82449274 | A | G | 6 | a0001c0001t0006g0071 a0001c0001t0006g0072 a0001c0001t0006g0073 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+1253A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449274 | |||||||
| chr4:82449421 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG01257.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.186+1400C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449421 | |||||||
| chr4:82449478 | C | T | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0002c0002t0001g0169 |
3 | HG00323.hp2 HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.186+1457C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449478 | |||||||
| chr4:82449536 | T | C | 31 | a0001c0001t0001g0255 a0001c0001t0002g0019 a0001c0001t0002g0020 others(28): Show |
35 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.187-1507T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449536 | |||||||
| chr4:82449569 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.187-1474T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449569 | |||||||
| chr4:82449658 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0057 |
3 | HG02809.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.187-1385T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449658 | |||||||
| chr4:82449681 | A | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0046 others(26): Show |
34 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.187-1362A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449681 | |||||||
| chr4:82449763 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187-1280T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449763 | |||||||
| chr4:82449764 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187-1279C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449764 | |||||||
| chr4:82449788 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.187-1255C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449788 | |||||||
| chr4:82449942 | A | G | 38 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0135 others(35): Show |
40 | HG00140.hp2 HG00323.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.187-1101A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82449942 | |||||||
| chr4:82450144 | T | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0254 |
2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.187-899T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450144 | |||||||
| chr4:82450163 | G | A | 41 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(38): Show |
44 | HG00140.hp2 HG00597.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.187-880G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450163 | |||||||
| chr4:82450192 | G | T | 8 | a0001c0001t0001g0014 a0001c0001t0003g0264 a0001c0001t0004g0161 others(5): Show |
9 | HG02145.hp2 HG02559.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.187-851G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450192 | |||||||
| chr4:82450234 | T | C | 28 | a0001c0001t0001g0036 a0001c0001t0001g0133 a0001c0001t0001g0224 others(25): Show |
32 | HG00609.hp1 HG00621.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.187-809T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450234 | |||||||
| chr4:82450244 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.187-799C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450244 | |||||||
| chr4:82450323 | G | A | 6 | a0001c0001t0001g0154 a0001c0001t0001g0242 a0001c0001t0004g0138 others(3): Show |
6 | HG02132.hp2 HG02165.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-720G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450323 | |||||||
| chr4:82450431 | T | C | 1 | a0001c0001t0005g0096 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.187-612T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 2/5 | chr4 | 82450431 | |||||||
| chr4:82451318 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.389+73T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451318 | |||||||
| chr4:82451492 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.389+247G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451492 | |||||||
| chr4:82451812 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.389+567G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451812 | |||||||
| chr4:82451815 | C | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0036 others(17): Show |
24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+570C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451815 | |||||||
| chr4:82451903 | C | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0039 others(9): Show |
15 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.389+658C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82451903 | |||||||
| chr4:82451960 | TAGTAC | T | 20 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0036 others(17): Show |
24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+718_389+722del others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82451960 | ||||||
| chr4:82452015 | G | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0036 others(17): Show |
24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+770G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452015 | |||||||
| chr4:82452061 | G | A | 3 | a0001c0001t0007g0016 a0001c0001t0007g0069 a0001c0001t0007g0070 |
4 | HG01884.hp2 HG02717.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.389+816G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452061 | |||||||
| chr4:82452082 | AT | A | 20 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0036 others(17): Show |
24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+850delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82452082 | ||||||
| chr4:82452104 | G | T | 6 | a0001c0001t0004g0044 a0001c0001t0004g0045 a0001c0001t0004g0050 others(3): Show |
6 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.389+859G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452104 | |||||||
| chr4:82452334 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+1089G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452334 | |||||||
| chr4:82452383 | A | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0036 others(17): Show |
24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.389+1138A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452383 | |||||||
| chr4:82452479 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.389+1234A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452479 | |||||||
| chr4:82452516 | T | C | 33 | a0001c0001t0001g0051 a0001c0001t0002g0114 a0001c0001t0002g0116 others(30): Show |
38 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.389+1271T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452516 | |||||||
| chr4:82452594 | A | G | 65 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(62): Show |
76 | HG00323.hp2 HG01106.hp1 HG01123.hp1 others(73): Show |
intron_variant | MODIFIER | c.389+1349A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452594 | |||||||
| chr4:82452707 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.389+1462C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452707 | |||||||
| chr4:82452775 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0002g0102 |
2 | HG02015.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.389+1530C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452775 | |||||||
| chr4:82452869 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.389+1624T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452869 | |||||||
| chr4:82452877 | T | C | 104 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(101): Show |
117 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.389+1632T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452877 | |||||||
| chr4:82452885 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.389+1640G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452885 | |||||||
| chr4:82452900 | C | CT | 10 | a0001c0001t0001g0048 a0001c0001t0001g0066 a0001c0001t0001g0136 others(7): Show |
10 | HG01243.hp1 HG02015.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.389+1674dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82452900 | ||||||
| chr4:82452900 | CT | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0182 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+1674delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82452900 | ||||||
| chr4:82452918 | T | C | 29 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0036 others(26): Show |
34 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.389+1673T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452918 | |||||||
| chr4:82452918 | T | TC | 62 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0057 others(59): Show |
69 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.389+1673_389+1674i others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452918 | |||||||
| chr4:82452918 | T | TTC | 13 | a0001c0001t0003g0163 a0001c0001t0004g0044 a0001c0001t0004g0045 others(10): Show |
14 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.389+1674_389+1675i others(4): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82452918 | ||||||
| chr4:82452994 | T | C | 2 | a0001c0001t0005g0017 a0001c0001t0005g0083 |
3 | HG00609.hp1 NA18960.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.390-1728T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82452994 | |||||||
| chr4:82453059 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.390-1663G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453059 | |||||||
| chr4:82453059 | G | T | 6 | a0001c0001t0003g0029 a0001c0001t0003g0168 a0001c0001t0003g0186 others(3): Show |
7 | HG00423.hp1 HG01109.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.390-1663G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453059 | |||||||
| chr4:82453118 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.390-1604C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453118 | |||||||
| chr4:82453118 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.390-1604C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453118 | |||||||
| chr4:82453178 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0218 |
2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.390-1544A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453178 | |||||||
| chr4:82453316 | T | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(14): Show |
24 | HG01106.hp1 HG01123.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.390-1406T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453316 | |||||||
| chr4:82453320 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390-1402T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453320 | |||||||
| chr4:82453598 | T | C | 1 | a0001c0001t0006g0021 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.390-1124T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453598 | |||||||
| chr4:82453636 | A | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
5 | HG02809.hp2 HG03209.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.390-1086A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453636 | |||||||
| chr4:82453695 | T | A | 10 | a0001c0001t0001g0128 a0001c0001t0001g0143 a0001c0001t0001g0194 others(7): Show |
11 | HG00323.hp2 HG01884.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.390-1027T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453695 | |||||||
| chr4:82453732 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.390-990C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453732 | |||||||
| chr4:82453884 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.390-838A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82453884 | |||||||
| chr4:82454050 | TA | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.390-655delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82454050 | ||||||
| chr4:82454050 | TAA | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0135 others(4): Show |
7 | HG02280.hp1 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.390-656_390-655del others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr4 | 82454050 | ||||||
| chr4:82454178 | C | T | 10 | a0001c0001t0004g0044 a0001c0001t0004g0045 a0001c0001t0004g0049 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.390-544C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454178 | |||||||
| chr4:82454257 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-465C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454257 | |||||||
| chr4:82454258 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-464T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454258 | |||||||
| chr4:82454259 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-463T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454259 | |||||||
| chr4:82454260 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-462T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454260 | |||||||
| chr4:82454261 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-461G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454261 | |||||||
| chr4:82454262 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-460A>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454262 | |||||||
| chr4:82454263 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-459G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454263 | |||||||
| chr4:82454265 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-457C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454265 | |||||||
| chr4:82454266 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-456T>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454266 | |||||||
| chr4:82454270 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-452A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454270 | |||||||
| chr4:82454272 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.390-450C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454272 | |||||||
| chr4:82454273 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0117 others(4): Show |
8 | HG02886.hp1 HG03130.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-449T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454273 | |||||||
| chr4:82454291 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.390-431G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454291 | |||||||
| chr4:82454566 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.390-156T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454566 | |||||||
| chr4:82454593 | G | A | 20 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0036 others(17): Show |
24 | HG00735.hp1 HG01069.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.390-129G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 3/5 | chr4 | 82454593 | |||||||
| chr4:82454945 | CT | C | 36 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0003g0029 others(33): Show |
41 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.522+103delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82454945 | ||||||
| chr4:82454995 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.522+141T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82454995 | |||||||
| chr4:82455149 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.522+295C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455149 | |||||||
| chr4:82455503 | G | A | 10 | a0001c0001t0004g0044 a0001c0001t0004g0045 a0001c0001t0004g0049 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+649G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455503 | |||||||
| chr4:82455528 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.522+674T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455528 | |||||||
| chr4:82455556 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.522+702G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455556 | |||||||
| chr4:82455596 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.522+742T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455596 | |||||||
| chr4:82455608 | G | A | 1 | a0001c0001t0006g0021 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.522+754G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455608 | |||||||
| chr4:82455624 | CA | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.522+782delA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82455624 | ||||||
| chr4:82455626 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.522+772A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455626 | |||||||
| chr4:82455647 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.522+793G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455647 | |||||||
| chr4:82455741 | G | A | 6 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0063 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+887G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455741 | |||||||
| chr4:82455785 | C | CA | 7 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0216 others(4): Show |
10 | HG01123.hp1 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+944dupA | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82455785 | ||||||
| chr4:82455817 | C | A | 6 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0063 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.522+963C>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82455817 | |||||||
| chr4:82456054 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.523-861C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456054 | |||||||
| chr4:82456178 | A | AT | 9 | a0001c0001t0001g0143 a0001c0001t0001g0156 a0001c0001t0001g0194 others(6): Show |
10 | HG00323.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-736dupT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82456178 | ||||||
| chr4:82456215 | CT | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.523-684delT | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82456215 | ||||||
| chr4:82456215 | CTT | C | 8 | a0001c0001t0001g0051 a0001c0001t0001g0121 a0001c0001t0001g0126 others(5): Show |
9 | HG02145.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.523-685_523-684del others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 82456215 | ||||||
| chr4:82456257 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.523-658T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456257 | |||||||
| chr4:82456353 | A | T | 1 | a0001c0001t0001g0240 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.523-562A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456353 | |||||||
| chr4:82456527 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
8 | HG02809.hp2 HG02886.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.523-388C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456527 | |||||||
| chr4:82456528 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.523-387G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456528 | |||||||
| chr4:82456768 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.523-147A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456768 | |||||||
| chr4:82456866 | G | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0131 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-49G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 4/5 | chr4 | 82456866 | |||||||
| chr4:82457432 | T | G | 1 | a0001c0001t0001g0268 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.646+394T>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457432 | |||||||
| chr4:82457480 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(11): Show |
20 | HG01106.hp1 HG01123.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.646+442C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457480 | |||||||
| chr4:82457530 | T | C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0062 others(5): Show |
9 | HG01167.hp1 HG01515.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.646+492T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457530 | |||||||
| chr4:82457571 | C | T | 2 | a0001c0001t0004g0049 a0001c0001t0004g0063 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.646+533C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457571 | |||||||
| chr4:82457618 | T | TAC | 6 | a0001c0001t0004g0049 a0001c0001t0004g0050 a0001c0001t0004g0063 others(3): Show |
7 | HG02145.hp2 HG02559.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.646+595_646+596dup others(2): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 82457618 | ||||||
| chr4:82457618 | T | TACAC | 5 | a0001c0001t0004g0044 a0001c0001t0004g0045 a0001c0001t0004g0124 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.646+593_646+596dup others(4): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 82457618 | ||||||
| chr4:82457719 | G | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.646+681G>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457719 | |||||||
| chr4:82457755 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.646+717G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457755 | |||||||
| chr4:82457768 | T | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(14): Show |
24 | HG01106.hp1 HG01123.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.646+730T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457768 | |||||||
| chr4:82457777 | C | T | 4 | a0001c0001t0004g0044 a0001c0001t0004g0045 a0001c0001t0004g0124 others(1): Show |
4 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.646+739C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82457777 | |||||||
| chr4:82458009 | C | T | 6 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0131 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.646+971C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458009 | |||||||
| chr4:82458073 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.646+1035A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458073 | |||||||
| chr4:82458077 | A | AGGCGGTG others(1): Show |
177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.646+1042_646+1043i others(10): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 82458077 | ||||||
| chr4:82458249 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.646+1211A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458249 | |||||||
| chr4:82458380 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.646+1342G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458380 | |||||||
| chr4:82458489 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.646+1451G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458489 | |||||||
| chr4:82458650 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.647-1331G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458650 | |||||||
| chr4:82458659 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.647-1322C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458659 | |||||||
| chr4:82458673 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.647-1308T>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458673 | |||||||
| chr4:82458914 | TGAG | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
8 | HG02809.hp2 HG02886.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.647-1062_647-1060d others(5): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 82458914 | ||||||
| chr4:82458948 | C | T | 1 | a0001c0001t0003g0205 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.647-1033C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82458948 | |||||||
| chr4:82459061 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.647-920C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459061 | |||||||
| chr4:82459087 | A | G | 3 | a0001c0001t0001g0230 a0001c0001t0002g0094 a0001c0001t0002g0099 |
3 | HG01361.hp2 HG02055.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.647-894A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459087 | |||||||
| chr4:82459148 | C | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0183 others(4): Show |
10 | HG00597.hp2 HG02015.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.647-833C>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459148 | |||||||
| chr4:82459512 | C | T | 1 | a0001c0001t0006g0111 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.647-469C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459512 | |||||||
| chr4:82459655 | A | G | 11 | a0001c0001t0001g0128 a0001c0001t0001g0143 a0001c0001t0001g0156 others(8): Show |
12 | HG00323.hp2 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.647-326A>G | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459655 | |||||||
| chr4:82459728 | G | C | 1 | a0001c0001t0001g0283 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.647-253G>C | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459728 | |||||||
| chr4:82459757 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.647-224C>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459757 | |||||||
| chr4:82459803 | C | CTTT | 4 | a0001c0001t0001g0245 a0001c0001t0001g0266 a0001c0001t0001g0273 others(1): Show |
4 | HG00408.hp2 HG02015.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.647-178_647-177ins others(3): Show |
ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459803 | |||||||
| chr4:82459804 | A | T | 4 | a0001c0001t0001g0245 a0001c0001t0001g0266 a0001c0001t0001g0273 others(1): Show |
4 | HG00408.hp2 HG02015.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.647-177A>T | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459804 | |||||||
| chr4:82459916 | G | A | 1 | a0001c0001t0006g0073 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.647-65G>A | ENOPH1 | ENSG00000145293.17 | transcript | ENST00000273920.8 | protein_coding | 5/5 | chr4 | 82459916 |