Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2053 |
| ensemblid | ENSG00000120915.14 |
| hgncid | 3402 |
| symbol | EPHX2 |
| name | epoxide hydrolase 2 |
| refseq_nuc | NM_001979.6 |
| refseq_prot | NP_001970.2 |
| ensembl_nuc | ENST00000521400.6 |
| ensembl_prot | ENSP00000430269.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 27491143 |
| end | 27545564 |
| strand | + |
| ver | v1.2 |
| region | chr8:27491143-27545564 |
| region5000 | chr8:27486143-27550564 |
| regionname0 | EPHX2_chr8_27491143_27545564 |
| regionname5000 | EPHX2_chr8_27486143_27550564 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 555 | 244 | 56 | 36 | 117 | 6 | 27 | 87 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0002 | 0/0 | 555 | 62 | 5 | 5 | 43 | 3 | 6 | 38 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0003 | 0/0 | 555 | 26 | 17 | 5 | 0 | 0 | 4 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0004 | 0/0 | 555 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0005 | 0/0 | 555 | 7 | 0 | 0 | 7 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0006 | 0/0 | 555 | 6 | 1 | 3 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0007 | 0/0 | 556 | 4 | 0 | 2 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(551): Show |
chr8 | 27486143 | 27550564 |
| a0008 | 0/0 | 555 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0009 | 0/0 | 556 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(551): Show |
chr8 | 27486143 | 27550564 |
| a0010 | 0/0 | 555 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0011 | 0/0 | 555 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0012 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0013 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0014 | 0/0 | 555 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0015 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0016 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0017 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0018 | 0/0 | 555 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| a0019 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | MTLRA others(550): Show |
chr8 | 27486143 | 27550564 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1665 | 137 | 14 | 32 | 66 | 4 | 19 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0001c0002 | 0/0 | 1665 | 59 | 8 | 2 | 40 | 2 | 7 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0001c0004 | 0/0 | 1665 | 21 | 21 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0001c0005 | 0/0 | 1665 | 16 | 10 | 0 | 6 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0001c0013 | 0/0 | 1665 | 3 | 0 | 0 | 3 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0001c0014 | 0/0 | 1665 | 3 | 2 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0001c0017 | 0/0 | 1665 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0001c0025 | 0/0 | 1665 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0001c0031 | 0/0 | 1665 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0001c0032 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0002c0003 | 0/0 | 1665 | 49 | 5 | 4 | 33 | 1 | 6 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0002c0008 | 0/0 | 1665 | 9 | 0 | 1 | 8 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0002c0011 | 0/0 | 1665 | 4 | 0 | 0 | 2 | 2 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0003c0006 | 0/0 | 1665 | 13 | 5 | 4 | 0 | 0 | 4 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0003c0007 | 0/0 | 1665 | 12 | 11 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0003c0035 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0004c0010 | 0/0 | 1665 | 7 | 5 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0004c0015 | 0/0 | 1665 | 3 | 3 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0005c0009 | 0/0 | 1665 | 7 | 0 | 0 | 7 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0006c0016 | 0/0 | 1665 | 3 | 0 | 3 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0006c0020 | 0/0 | 1665 | 2 | 1 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0006c0021 | 0/0 | 1665 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0007c0012 | 0/0 | 1668 | 3 | 0 | 2 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1663): Show |
chr8 | 27486143 | 27550564 | ||
| a0007c0029 | 0/0 | 1668 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1663): Show |
chr8 | 27486143 | 27550564 | ||
| a0008c0019 | 0/0 | 1665 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0008c0034 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0009c0018 | 0/0 | 1668 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1663): Show |
chr8 | 27486143 | 27550564 | ||
| a0010c0033 | 0/0 | 1665 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0011c0027 | 0/0 | 1665 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0012c0023 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0013c0037 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0014c0030 | 0/0 | 1665 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0015c0036 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0016c0024 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0017c0022 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0018c0028 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 | ||
| a0019c0026 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | ATGAC others(1660): Show |
chr8 | 27486143 | 27550564 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2776 | 133 | 14 | 31 | 64 | 4 | 18 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0001t0006 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0001t0009 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0001t0010 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0001t0011 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0002t0002 | 0/0 | 2776 | 59 | 8 | 2 | 40 | 2 | 7 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0004t0003 | 0/0 | 2776 | 12 | 12 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0004t0004 | 0/0 | 2776 | 9 | 9 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0005t0002 | 0/0 | 2776 | 6 | 6 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0005t0003 | 0/0 | 2776 | 8 | 4 | 0 | 4 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0005t0005 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0005t0006 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0013t0002 | 0/0 | 2776 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0013t0006 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0014t0003 | 0/0 | 2776 | 3 | 2 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0017t0001 | 0/0 | 2776 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0025t0001 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0031t0001 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0001c0032t0003 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0002c0003t0002 | 0/0 | 2776 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0002c0003t0003 | 0/0 | 2776 | 44 | 5 | 4 | 28 | 1 | 6 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0002c0003t0005 | 0/0 | 2776 | 3 | 0 | 0 | 3 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0002c0008t0002 | 0/0 | 2776 | 9 | 0 | 1 | 8 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0002c0011t0001 | 0/0 | 2776 | 4 | 0 | 0 | 2 | 2 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0003c0006t0002 | 0/0 | 2776 | 13 | 5 | 4 | 0 | 0 | 4 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0003c0007t0004 | 0/0 | 2776 | 9 | 8 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0003c0007t0008 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0003c0007t0012 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0003c0035t0001 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0004c0010t0001 | 0/0 | 2776 | 5 | 3 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0004c0010t0007 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0004c0015t0002 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0004c0015t0004 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0005c0009t0001 | 0/0 | 2776 | 7 | 0 | 0 | 7 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0006c0016t0001 | 0/0 | 2776 | 3 | 0 | 3 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0006c0020t0001 | 0/0 | 2776 | 2 | 1 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0006c0021t0001 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0007c0012t0001 | 0/0 | 2779 | 3 | 0 | 2 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2774): Show |
chr8 | 27486143 | 27550564 |
| a0007c0029t0003 | 0/0 | 2779 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2774): Show |
chr8 | 27486143 | 27550564 |
| a0008c0019t0001 | 0/0 | 2776 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0008c0034t0003 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0009c0018t0001 | 0/0 | 2779 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2774): Show |
chr8 | 27486143 | 27550564 |
| a0010c0033t0004 | 0/0 | 2776 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0011c0027t0001 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0012c0023t0003 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0013c0037t0004 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0014c0030t0001 | 0/0 | 2776 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0015c0036t0002 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0016c0024t0002 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0017c0022t0002 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0018c0028t0001 | 0/0 | 2776 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| a0019c0026t0002 | 0/0 | 2776 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | GCCCT others(2771): Show |
chr8 | 27486143 | 27550564 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0009g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0010g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0001t0011g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0004t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0005t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0013t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0013t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0013t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0014t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0014t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0014t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0017t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0017t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0025t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0031t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0001c0032t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0003t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0008t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0008t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0008t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0008t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0008t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0008t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0008t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0008t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0011t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0011t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0011t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0002c0011t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0006t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0008g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0007t0012g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0003c0035t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0010t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0010t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0010t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0010t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0010t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0010t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0010t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0015t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0015t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0004c0015t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0005c0009t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0005c0009t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0005c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0005c0009t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0005c0009t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0005c0009t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0006c0016t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0006c0016t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0006c0020t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0006c0020t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0006c0021t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0007c0012t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0007c0012t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0007c0012t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0007c0029t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0008c0019t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0008c0034t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0009c0018t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0009c0018t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0010c0033t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0011c0027t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0012c0023t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0013c0037t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0014c0030t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0015c0036t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0016c0024t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0017c0022t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0018c0028t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| a0019c0026t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0003 | t0003 | g0049 | EUR | GBR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00323 | hp1 | a0006 | c0020 | t0001 | g0008 | EUR | FIN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00408 | hp2 | a0001 | c0005 | t0003 | g0137 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00544 | hp1 | a0002 | c0003 | t0003 | g0066 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00558 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00597 | hp2 | a0005 | c0009 | t0001 | g0016 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00621 | hp2 | a0005 | c0009 | t0001 | g0016 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00639 | hp1 | a0009 | c0018 | t0001 | g0269 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00639 | hp2 | a0004 | c0010 | t0001 | g0264 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00642 | hp1 | a0003 | c0006 | t0002 | g0306 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00673 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00733 | hp1 | a0003 | c0007 | t0004 | g0278 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00733 | hp2 | a0001 | c0031 | t0001 | g0147 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00738 | hp2 | a0010 | c0033 | t0004 | g0043 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01070 | hp1 | a0007 | c0012 | t0001 | g0266 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01106 | hp1 | a0003 | c0006 | t0002 | g0311 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01109 | hp1 | a0009 | c0018 | t0001 | g0267 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01167 | hp1 | a0003 | c0006 | t0002 | g0308 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01192 | hp1 | a0002 | c0003 | t0003 | g0065 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01192 | hp2 | a0004 | c0010 | t0001 | g0258 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01243 | hp2 | a0001 | c0014 | t0003 | g0298 | AMR | PUR | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01257 | hp1 | a0006 | c0016 | t0001 | g0008 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01258 | hp1 | a0006 | c0016 | t0001 | g0008 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01261 | hp2 | a0002 | c0003 | t0003 | g0207 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01361 | hp1 | a0006 | c0016 | t0001 | g0160 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0228 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01515 | hp2 | a0011 | c0027 | t0001 | g0170 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01516 | hp1 | a0002 | c0011 | t0001 | g0201 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0229 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01517 | hp2 | a0002 | c0011 | t0001 | g0202 | EUR | IBS | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01884 | hp2 | a0001 | c0004 | t0003 | g0293 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01891 | hp2 | a0003 | c0006 | t0002 | g0303 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01928 | hp2 | a0002 | c0008 | t0002 | g0079 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01943 | hp2 | a0001 | c0001 | t0011 | g0025 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01978 | hp1 | a0007 | c0012 | t0001 | g0268 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG01981 | hp2 | a0002 | c0003 | t0003 | g0063 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0247 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02015 | hp1 | a0001 | c0005 | t0005 | g0215 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02015 | hp2 | a0001 | c0005 | t0003 | g0071 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02027 | hp2 | a0001 | c0013 | t0002 | g0233 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02055 | hp2 | a0001 | c0004 | t0004 | g0296 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0106 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02080 | hp1 | a0005 | c0009 | t0001 | g0089 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02083 | hp1 | a0012 | c0023 | t0003 | g0001 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02129 | hp1 | a0005 | c0009 | t0001 | g0088 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02132 | hp2 | a0005 | c0009 | t0001 | g0087 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02145 | hp1 | a0013 | c0037 | t0004 | g0044 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | CDX | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02165 | hp2 | a0001 | c0005 | t0003 | g0301 | EAS | CDX | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02257 | hp1 | a0001 | c0004 | t0003 | g0035 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02257 | hp2 | a0003 | c0007 | t0004 | g0286 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02258 | hp1 | a0001 | c0032 | t0003 | g0039 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02258 | hp2 | a0001 | c0004 | t0004 | g0290 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02280 | hp2 | a0003 | c0006 | t0002 | g0309 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02293 | hp1 | a0003 | c0006 | t0002 | g0302 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02300 | hp2 | a0002 | c0003 | t0003 | g0005 | AMR | PEL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02451 | hp1 | a0002 | c0003 | t0003 | g0205 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02523 | hp1 | a0007 | c0029 | t0003 | g0300 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02523 | hp2 | a0007 | c0012 | t0001 | g0265 | EAS | KHV | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02572 | hp1 | a0001 | c0005 | t0003 | g0096 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02572 | hp2 | a0004 | c0015 | t0004 | g0255 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0231 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02615 | hp1 | a0003 | c0007 | t0004 | g0281 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02615 | hp2 | a0002 | c0003 | t0003 | g0028 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02622 | hp2 | a0004 | c0010 | t0001 | g0263 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02630 | hp1 | a0003 | c0006 | t0002 | g0304 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02630 | hp2 | a0003 | c0035 | t0001 | g0307 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02647 | hp1 | a0008 | c0019 | t0001 | g0036 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02647 | hp2 | a0003 | c0007 | t0004 | g0280 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02683 | hp1 | a0003 | c0006 | t0002 | g0310 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02683 | hp2 | a0002 | c0003 | t0003 | g0048 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0222 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02723 | hp1 | a0003 | c0007 | t0008 | g0272 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02723 | hp2 | a0004 | c0015 | t0002 | g0259 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02809 | hp1 | a0001 | c0004 | t0003 | g0294 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02809 | hp2 | a0001 | c0005 | t0002 | g0093 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02818 | hp1 | a0003 | c0007 | t0004 | g0282 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02818 | hp2 | a0003 | c0007 | t0004 | g0287 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02886 | hp2 | a0003 | c0007 | t0004 | g0283 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02895 | hp2 | a0001 | c0005 | t0002 | g0092 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02896 | hp1 | a0001 | c0005 | t0002 | g0094 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0203 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0204 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02922 | hp1 | a0003 | c0007 | t0012 | g0284 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02922 | hp2 | a0004 | c0010 | t0001 | g0262 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02970 | hp1 | a0001 | c0004 | t0003 | g0035 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02970 | hp2 | a0003 | c0007 | t0008 | g0273 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02976 | hp1 | a0004 | c0010 | t0007 | g0261 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02976 | hp2 | a0001 | c0004 | t0003 | g0010 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03041 | hp1 | a0001 | c0004 | t0003 | g0011 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03041 | hp2 | a0001 | c0005 | t0002 | g0017 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03098 | hp1 | a0001 | c0004 | t0004 | g0295 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03098 | hp2 | a0001 | c0014 | t0003 | g0297 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03130 | hp1 | a0001 | c0004 | t0004 | g0037 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0028 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03139 | hp1 | a0003 | c0006 | t0002 | g0277 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03195 | hp1 | a0001 | c0005 | t0002 | g0214 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0252 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03209 | hp1 | a0003 | c0006 | t0002 | g0276 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03225 | hp1 | a0001 | c0004 | t0004 | g0038 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03225 | hp2 | a0001 | c0005 | t0003 | g0097 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03453 | hp1 | a0001 | c0004 | t0003 | g0288 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03486 | hp2 | a0001 | c0004 | t0003 | g0011 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0012 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03516 | hp1 | a0004 | c0010 | t0007 | g0260 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03516 | hp2 | a0002 | c0003 | t0003 | g0206 | AFR | ESN | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03540 | hp1 | a0001 | c0004 | t0003 | g0010 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03540 | hp2 | a0001 | c0004 | t0004 | g0037 | AFR | GWD | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03579 | hp2 | a0008 | c0034 | t0003 | g0011 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03669 | hp1 | a0003 | c0006 | t0002 | g0312 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03669 | hp2 | a0002 | c0003 | t0003 | g0056 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03710 | hp1 | a0002 | c0003 | t0003 | g0068 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0237 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0221 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03942 | hp1 | a0002 | c0003 | t0003 | g0274 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG04115 | hp2 | a0003 | c0006 | t0002 | g0313 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0031 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG04199 | hp1 | a0001 | c0001 | t0010 | g0144 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG04199 | hp2 | a0001 | c0025 | t0001 | g0244 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG04228 | hp1 | a0014 | c0030 | t0001 | g0100 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG04228 | hp2 | a0002 | c0003 | t0003 | g0082 | SAS | STU | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18522 | hp1 | a0001 | c0014 | t0003 | g0299 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18522 | hp2 | a0001 | c0004 | t0003 | g0010 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18612 | hp1 | a0002 | c0003 | t0003 | g0073 | EAS | CHB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18612 | hp2 | a0005 | c0009 | t0001 | g0090 | EAS | CHB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18747 | hp1 | a0002 | c0011 | t0001 | g0072 | EAS | CHB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18747 | hp2 | a0001 | c0005 | t0003 | g0171 | EAS | CHB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18906 | hp1 | a0001 | c0004 | t0003 | g0039 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0209 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18941 | hp1 | a0002 | c0003 | t0003 | g0076 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18942 | hp2 | a0002 | c0008 | t0002 | g0057 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18943 | hp1 | a0005 | c0009 | t0001 | g0186 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18943 | hp2 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18944 | hp2 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18945 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18946 | hp2 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18949 | hp1 | a0001 | c0001 | t0009 | g0026 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18950 | hp1 | a0002 | c0003 | t0002 | g0083 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18950 | hp2 | a0015 | c0036 | t0002 | g0055 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18951 | hp1 | a0001 | c0017 | t0001 | g0193 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18952 | hp1 | a0002 | c0003 | t0003 | g0052 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18961 | hp1 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18969 | hp1 | a0002 | c0003 | t0005 | g0064 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18970 | hp1 | a0002 | c0003 | t0003 | g0084 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18972 | hp1 | a0002 | c0003 | t0005 | g0081 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18973 | hp1 | a0002 | c0003 | t0003 | g0074 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18978 | hp1 | a0016 | c0024 | t0002 | g0032 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18978 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18980 | hp2 | a0002 | c0003 | t0003 | g0067 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18983 | hp2 | a0002 | c0008 | t0002 | g0061 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18984 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18984 | hp2 | a0002 | c0008 | t0002 | g0062 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18985 | hp2 | a0002 | c0003 | t0003 | g0085 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18989 | hp2 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18991 | hp2 | a0002 | c0008 | t0002 | g0060 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18994 | hp1 | a0002 | c0003 | t0003 | g0080 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19000 | hp1 | a0002 | c0003 | t0003 | g0086 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19002 | hp2 | a0001 | c0013 | t0006 | g0046 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19030 | hp2 | a0001 | c0005 | t0003 | g0098 | AFR | LWK | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19054 | hp1 | a0002 | c0008 | t0002 | g0013 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19056 | hp1 | a0002 | c0003 | t0002 | g0070 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19058 | hp1 | a0017 | c0022 | t0002 | g0238 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19058 | hp2 | a0018 | c0028 | t0001 | g0178 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19062 | hp2 | a0002 | c0003 | t0003 | g0054 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19064 | hp2 | a0001 | c0017 | t0001 | g0190 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19065 | hp1 | a0001 | c0005 | t0006 | g0102 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19066 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19068 | hp2 | a0002 | c0008 | t0002 | g0013 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19072 | hp1 | a0002 | c0008 | t0002 | g0058 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19074 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19075 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19079 | hp1 | a0002 | c0003 | t0005 | g0059 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19081 | hp1 | a0002 | c0003 | t0003 | g0053 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19081 | hp2 | a0002 | c0003 | t0003 | g0077 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19083 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19083 | hp2 | a0002 | c0011 | t0001 | g0181 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19085 | hp1 | a0002 | c0003 | t0003 | g0075 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19087 | hp1 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19090 | hp2 | a0001 | c0013 | t0002 | g0045 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19240 | hp1 | a0001 | c0004 | t0004 | g0292 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0208 | AFR | YRI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA20129 | hp1 | a0001 | c0004 | t0004 | g0038 | AFR | ASW | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA20129 | hp2 | a0004 | c0015 | t0004 | g0254 | AFR | ASW | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA20752 | hp1 | a0006 | c0021 | t0001 | g0003 | EUR | TSI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA20905 | hp1 | a0002 | c0003 | t0003 | g0069 | SAS | GIH | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA20905 | hp2 | a0003 | c0006 | t0002 | g0305 | SAS | GIH | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02486 | hp1 | a0001 | c0005 | t0002 | g0017 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02486 | hp2 | a0001 | c0004 | t0004 | g0291 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG02559 | hp2 | a0003 | c0007 | t0004 | g0285 | AFR | ACB | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03471 | hp1 | a0003 | c0007 | t0004 | g0279 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG03471 | hp2 | a0001 | c0004 | t0003 | g0289 | AFR | MSL | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG06807 | hp1 | a0001 | c0005 | t0003 | g0095 | AFR | USA | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| HG06807 | hp2 | a0008 | c0019 | t0001 | g0036 | AFR | USA | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA18955 | hp2 | a0002 | c0008 | t0002 | g0078 | EAS | JPT | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | USA | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA20300 | hp2 | a0019 | c0026 | t0002 | g0256 | AFR | USA | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA21309 | hp1 | a0004 | c0010 | t0001 | g0257 | AFR | LWK | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| NA21309 | hp2 | a0006 | c0020 | t0001 | g0109 | AFR | LWK | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0271 | REF | REF | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0198 | REF | REF | EPHX2_chr8_27486143_27550564 | EPHX2 | chr8 | 27486143 | 27550564 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27500978 | C | T | 3 | a0006 a0013 a0015 |
7 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
missense_variant | MODERATE | c.154C>T | p.Arg52Trp | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/19 | 220/2776 | 154/1668 | 52/555 | chr8 | 27500978 | |||
| chr8:27500979 | G | A | 1 | a0006 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.155G>A | p.Arg52Gln | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/19 | 221/2776 | 155/1668 | 52/555 | chr8 | 27500979 | |||
| chr8:27500988 | A | G | 1 | a0003 | 26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
missense_variant | MODERATE | c.164A>G | p.Lys55Arg | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/19 | 230/2776 | 164/1668 | 55/555 | chr8 | 27500988 | |||
| chr8:27503683 | A | G | 1 | a0008 | 3 | HG02647.hp1 HG03579.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.266A>G | p.Lys89Arg | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/19 | 332/2776 | 266/1668 | 89/555 | chr8 | 27503683 | |||
| chr8:27503724 | C | T | 3 | a0004 a0010 a0013 |
12 | HG00639.hp2 HG00738.hp2 HG01192.hp2 others(9): Show |
missense_variant | MODERATE | c.307C>T | p.Arg103Cys | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/19 | 373/2776 | 307/1668 | 103/555 | chr8 | 27503724 | |||
| chr8:27504998 | G | A | 1 | a0010 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.389G>A | p.Arg130His | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/19 | 455/2776 | 389/1668 | 130/555 | chr8 | 27504998 | |||
| chr8:27505070 | G | A | 1 | a0005 | 7 | HG00597.hp2 HG00621.hp2 HG02080.hp1 others(4): Show |
missense_variant | MODERATE | c.461G>A | p.Cys154Tyr | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/19 | 527/2776 | 461/1668 | 154/555 | chr8 | 27505070 | |||
| chr8:27515778 | G | A | 1 | a0017 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.796G>A | p.Gly266Arg | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/19 | 862/2776 | 796/1668 | 266/555 | chr8 | 27515778 | |||
| chr8:27516348 | G | A | 3 | a0002 a0012 a0015 |
64 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
missense_variant | MODERATE | c.860G>A | p.Arg287Gln | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/19 | 926/2776 | 860/1668 | 287/555 | chr8 | 27516348 | |||
| chr8:27525384 | C | T | 1 | a0014 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1081C>T | p.Pro361Ser | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/19 | 1147/2776 | 1081/1668 | 361/555 | chr8 | 27525384 | |||
| chr8:27525432 | G | A | 1 | a0009 | 2 | HG00639.hp1 HG01109.hp1 |
missense_variant | MODERATE | c.1129G>A | p.Ala377Thr | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/19 | 1195/2776 | 1129/1668 | 377/555 | chr8 | 27525432 | |||
| chr8:27536817 | A | AGTC | 2 | a0007 a0009 |
6 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(3): Show |
disruptive_inframe_insertion | MODERATE | c.1206_1208dupTCG | p.Arg403dup | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/19 | 1275/2776 | 1209/1668 | 403/555 | INFO_REALIGN_3_PRIME | chr8 | 27536817 | ||
| chr8:27536833 | G | A | 1 | a0012 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.1220G>A | p.Ser407Asn | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/19 | 1286/2776 | 1220/1668 | 407/555 | chr8 | 27536833 | |||
| chr8:27536833 | G | T | 1 | a0018 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1220G>T | p.Ser407Ile | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/19 | 1286/2776 | 1220/1668 | 407/555 | chr8 | 27536833 | |||
| chr8:27540575 | C | T | 1 | a0011 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.1298C>T | p.Pro433Leu | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/19 | 1364/2776 | 1298/1668 | 433/555 | chr8 | 27540575 | |||
| chr8:27541502 | A | G | 1 | a0019 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1409A>G | p.Glu470Gly | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/19 | 1475/2776 | 1409/1668 | 470/555 | chr8 | 27541502 | |||
| chr8:27543777 | C | A | 1 | a0016 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.1478C>A | p.Ala493Glu | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/19 | 1544/2776 | 1478/1668 | 493/555 | chr8 | 27543777 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27505098 | T | A | 1 | a0001c0017 | 2 | NA18951.hp1 NA19064.hp2 |
synonymous_variant | LOW | c.489T>A | p.Pro163Pro | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/19 | 555/2776 | 489/1668 | 163/555 | chr8 | 27505098 | |||
| chr8:27506925 | A | C | 5 | a0001c0004 a0001c0014 a0001c0032 others(2): Show |
28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
synonymous_variant | LOW | c.591A>C | p.Gly197Gly | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/19 | 657/2776 | 591/1668 | 197/555 | chr8 | 27506925 | |||
| chr8:27511862 | G | A | 1 | a0001c0014 | 3 | HG01243.hp2 HG03098.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.687G>A | p.Pro229Pro | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/19 | 753/2776 | 687/1668 | 229/555 | chr8 | 27511862 | |||
| chr8:27515753 | C | T | 1 | a0006c0016 | 3 | HG01257.hp1 HG01258.hp1 HG01361.hp1 |
synonymous_variant | LOW | c.771C>T | p.Ser257Ser | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/19 | 837/2776 | 771/1668 | 257/555 | chr8 | 27515753 | |||
| chr8:27516337 | G | A | 1 | a0009c0018 | 2 | HG00639.hp1 HG01109.hp1 |
synonymous_variant | LOW | c.849G>A | p.Gln283Gln | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/19 | 915/2776 | 849/1668 | 283/555 | chr8 | 27516337 | |||
| chr8:27518048 | A | G | 1 | a0009c0018 | 2 | HG00639.hp1 HG01109.hp1 |
synonymous_variant | LOW | c.921A>G | p.Glu307Glu | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/19 | 987/2776 | 921/1668 | 307/555 | chr8 | 27518048 | |||
| chr8:27522443 | C | T | 1 | a0001c0013 | 3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
synonymous_variant | LOW | c.993C>T | p.Phe331Phe | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/19 | 1059/2776 | 993/1668 | 331/555 | chr8 | 27522443 | |||
| chr8:27522497 | C | T | 1 | a0001c0031 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.1047C>T | p.Pro349Pro | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/19 | 1113/2776 | 1047/1668 | 349/555 | chr8 | 27522497 | |||
| chr8:27525365 | G | A | 1 | a0001c0032 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1062G>A | p.Ala354Ala | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/19 | 1128/2776 | 1062/1668 | 354/555 | chr8 | 27525365 | |||
| chr8:27536849 | C | T | 1 | a0003c0006 | 13 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(10): Show |
synonymous_variant | LOW | c.1236C>T | p.Ser412Ser | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/19 | 1302/2776 | 1236/1668 | 412/555 | chr8 | 27536849 | |||
| chr8:27538691 | G | A | 7 | a0001c0002 a0001c0025 a0002c0008 others(4): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
splice_region_variant&synonymous_variant | LOW | c.1275G>A | p.Ala425Ala | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/19 | 1341/2776 | 1275/1668 | 425/555 | chr8 | 27538691 | |||
| chr8:27544447 | A | C | 20 | a0001c0002 a0001c0004 a0001c0005 others(17): Show |
198 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
synonymous_variant | LOW | c.1593A>C | p.Pro531Pro | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 1659/2776 | 1593/1668 | 531/555 | chr8 | 27544447 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27491156 | C | T | 1 | a0003c0007t0008 | 2 | HG02723.hp1 HG02970.hp2 |
5_prime_UTR_variant | MODIFIER | c.-53C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/19 | 53 | chr8 | 27491156 | ||||||
| chr8:27544557 | A | G | 31 | a0001c0001t0006 a0001c0002t0002 a0001c0004t0003 others(28): Show |
199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*35A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 35 | chr8 | 27544557 | ||||||
| chr8:27544615 | T | C | 26 | a0001c0002t0002 a0001c0004t0003 a0001c0004t0004 others(23): Show |
193 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*93T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 93 | chr8 | 27544615 | ||||||
| chr8:27544736 | G | A | 2 | a0003c0007t0008 a0003c0007t0012 |
3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*214G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 214 | chr8 | 27544736 | ||||||
| chr8:27544750 | G | A | 1 | a0001c0001t0009 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 228 | chr8 | 27544750 | ||||||
| chr8:27544802 | G | A | 1 | a0001c0001t0010 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 280 | chr8 | 27544802 | ||||||
| chr8:27544977 | C | T | 18 | a0001c0002t0002 a0001c0004t0004 a0001c0005t0002 others(15): Show |
121 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*455C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 455 | chr8 | 27544977 | ||||||
| chr8:27545014 | G | A | 5 | a0001c0004t0004 a0003c0007t0004 a0004c0015t0004 others(2): Show |
22 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 492 | chr8 | 27545014 | ||||||
| chr8:27545147 | G | A | 13 | a0001c0002t0002 a0001c0005t0002 a0001c0013t0002 others(10): Show |
99 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*625G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 625 | chr8 | 27545147 | ||||||
| chr8:27545260 | G | A | 8 | a0001c0004t0003 a0001c0005t0003 a0001c0014t0003 others(5): Show |
71 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*738G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 738 | chr8 | 27545260 | ||||||
| chr8:27545497 | G | T | 5 | a0001c0004t0004 a0003c0007t0004 a0004c0015t0004 others(2): Show |
22 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*975G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 975 | chr8 | 27545497 | ||||||
| chr8:27545512 | A | G | 1 | a0001c0001t0011 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*990A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 990 | chr8 | 27545512 | ||||||
| chr8:27545536 | G | C | 1 | a0004c0010t0007 | 2 | HG02976.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1014G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 19/19 | 1014 | chr8 | 27545536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:27491377 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.101+68A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491377 | |||||||
| chr8:27491447 | C | G | 12 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(9): Show |
12 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+138C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491447 | |||||||
| chr8:27491849 | A | T | 2 | a0001c0005t0003g0301 a0007c0029t0003g0300 |
2 | HG02165.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.101+540A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491849 | |||||||
| chr8:27491883 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.101+574T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491883 | |||||||
| chr8:27491920 | A | G | 21 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0035 others(18): Show |
28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.101+611A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491920 | |||||||
| chr8:27491952 | G | GT | 30 | a0001c0001t0001g0275 a0001c0004t0004g0296 a0001c0014t0003g0297 others(27): Show |
30 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.101+655dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27491952 | ||||||
| chr8:27491952 | GT | G | 10 | a0001c0001t0001g0042 a0001c0004t0003g0010 a0001c0004t0003g0035 others(7): Show |
13 | HG00738.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.101+655delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27491952 | ||||||
| chr8:27491966 | T | G | 1 | a0003c0006t0002g0302 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101+657T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27491966 | |||||||
| chr8:27492019 | G | A | 1 | a0001c0002t0002g0012 | 2 | HG03490.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.101+710G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492019 | |||||||
| chr8:27492189 | G | T | 1 | a0013c0037t0004g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101+880G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492189 | |||||||
| chr8:27492271 | A | G | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+962A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492271 | |||||||
| chr8:27492321 | T | C | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+1012T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492321 | |||||||
| chr8:27492561 | A | C | 2 | a0001c0004t0003g0039 a0001c0032t0003g0039 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.101+1252A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492561 | |||||||
| chr8:27492587 | C | T | 1 | a0003c0007t0004g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.101+1278C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492587 | |||||||
| chr8:27492597 | G | A | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+1288G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492597 | |||||||
| chr8:27492739 | G | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101+1430G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492739 | |||||||
| chr8:27492814 | G | A | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.101+1505G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27492814 | |||||||
| chr8:27493047 | G | A | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+1738G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493047 | |||||||
| chr8:27493089 | A | C | 1 | a0001c0001t0001g0270 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.101+1780A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493089 | |||||||
| chr8:27493117 | C | G | 5 | a0007c0012t0001g0265 a0007c0012t0001g0266 a0007c0012t0001g0268 others(2): Show |
5 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1808C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493117 | |||||||
| chr8:27493209 | G | A | 4 | a0001c0004t0003g0011 a0001c0004t0003g0293 a0008c0019t0001g0036 others(1): Show |
6 | HG01884.hp2 HG02647.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+1900G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493209 | |||||||
| chr8:27493464 | T | C | 2 | a0002c0003t0003g0048 a0002c0003t0003g0049 |
2 | HG00140.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.101+2155T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493464 | |||||||
| chr8:27493502 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.101+2193G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493502 | |||||||
| chr8:27493648 | G | C | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+2339G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493648 | |||||||
| chr8:27493702 | T | TG | 113 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0245 others(110): Show |
134 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.101+2396dupG | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27493702 | ||||||
| chr8:27493881 | G | A | 1 | a0002c0003t0003g0048 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.101+2572G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493881 | |||||||
| chr8:27493994 | C | T | 1 | a0001c0005t0002g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.101+2685C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27493994 | |||||||
| chr8:27494081 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.101+2772A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494081 | |||||||
| chr8:27494165 | T | A | 2 | a0003c0006t0002g0303 a0003c0006t0002g0304 |
2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.101+2856T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494165 | |||||||
| chr8:27494181 | T | C | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101+2872T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494181 | |||||||
| chr8:27494221 | G | A | 44 | a0001c0005t0003g0071 a0002c0003t0002g0070 a0002c0003t0002g0083 others(41): Show |
56 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.101+2912G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494221 | |||||||
| chr8:27494290 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.101+2981C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494290 | |||||||
| chr8:27494291 | G | T | 2 | a0001c0014t0003g0298 a0001c0014t0003g0299 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.101+2982G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494291 | |||||||
| chr8:27494420 | A | G | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+3111A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494420 | |||||||
| chr8:27494473 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.101+3164C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494473 | |||||||
| chr8:27494474 | T | G | 3 | a0002c0003t0003g0052 a0002c0003t0003g0053 a0002c0003t0003g0054 |
3 | NA18952.hp1 NA19062.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.101+3165T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494474 | |||||||
| chr8:27494506 | A | G | 2 | a0001c0005t0003g0301 a0007c0029t0003g0300 |
2 | HG02165.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.101+3197A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494506 | |||||||
| chr8:27494633 | T | C | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+3324T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494633 | |||||||
| chr8:27494714 | T | C | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+3405T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494714 | |||||||
| chr8:27494727 | G | A | 5 | a0005c0009t0001g0016 a0005c0009t0001g0087 a0005c0009t0001g0088 others(2): Show |
6 | HG00597.hp2 HG00621.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+3418G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494727 | |||||||
| chr8:27494741 | G | T | 1 | a0003c0007t0004g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.101+3432G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494741 | |||||||
| chr8:27494801 | A | T | 1 | a0001c0004t0004g0295 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.101+3492A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494801 | |||||||
| chr8:27494815 | G | A | 1 | a0003c0006t0002g0305 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101+3506G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494815 | |||||||
| chr8:27494944 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.101+3635G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27494944 | |||||||
| chr8:27495116 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.101+3807A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495116 | |||||||
| chr8:27495233 | A | G | 54 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0209 others(51): Show |
67 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.101+3924A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495233 | |||||||
| chr8:27495250 | T | A | 1 | a0010c0033t0004g0043 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.101+3941T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495250 | |||||||
| chr8:27495251 | C | T | 1 | a0010c0033t0004g0043 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.101+3942C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495251 | |||||||
| chr8:27495304 | A | T | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+3995A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495304 | |||||||
| chr8:27495326 | A | T | 5 | a0003c0007t0004g0282 a0003c0007t0004g0283 a0003c0007t0004g0285 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+4017A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495326 | |||||||
| chr8:27495373 | A | G | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.101+4064A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495373 | |||||||
| chr8:27495546 | A | G | 3 | a0003c0006t0002g0302 a0003c0006t0002g0312 a0003c0006t0002g0313 |
3 | HG02293.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.101+4237A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495546 | |||||||
| chr8:27495556 | G | A | 1 | a0002c0003t0003g0028 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.101+4247G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495556 | |||||||
| chr8:27495573 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.101+4264G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495573 | |||||||
| chr8:27495710 | A | G | 9 | a0001c0001t0001g0040 a0004c0010t0001g0257 a0004c0010t0001g0258 others(6): Show |
10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.101+4401A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495710 | |||||||
| chr8:27495802 | A | C | 1 | a0019c0026t0002g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.101+4493A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495802 | |||||||
| chr8:27495864 | G | C | 2 | a0003c0006t0002g0276 a0003c0006t0002g0277 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.101+4555G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495864 | |||||||
| chr8:27495998 | C | T | 1 | a0003c0006t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.101+4689C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27495998 | |||||||
| chr8:27496226 | C | A | 21 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0035 others(18): Show |
28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.102-4700C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496226 | |||||||
| chr8:27496346 | C | T | 10 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0003c0007t0004g0280 others(7): Show |
10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.102-4580C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496346 | |||||||
| chr8:27496620 | C | T | 1 | a0003c0007t0004g0286 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.102-4306C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496620 | |||||||
| chr8:27496862 | T | C | 50 | a0001c0001t0001g0245 a0001c0002t0002g0002 a0001c0002t0002g0004 others(47): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.102-4064T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496862 | |||||||
| chr8:27496901 | A | G | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.102-4025A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496901 | |||||||
| chr8:27496948 | G | T | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.102-3978G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496948 | |||||||
| chr8:27496954 | A | G | 113 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0245 others(110): Show |
134 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.102-3972A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496954 | |||||||
| chr8:27496983 | G | C | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.102-3943G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27496983 | |||||||
| chr8:27497072 | C | A | 4 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(1): Show |
6 | HG02055.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-3854C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497072 | |||||||
| chr8:27497094 | T | C | 122 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0245 others(119): Show |
144 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.102-3832T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497094 | |||||||
| chr8:27497184 | A | C | 1 | a0003c0006t0002g0305 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.102-3742A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497184 | |||||||
| chr8:27497234 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.102-3692T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497234 | |||||||
| chr8:27497404 | T | G | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.102-3522T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497404 | |||||||
| chr8:27497421 | C | G | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.102-3505C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497421 | |||||||
| chr8:27497518 | G | A | 4 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(1): Show |
7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-3408G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497518 | |||||||
| chr8:27497613 | T | C | 113 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0245 others(110): Show |
134 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.102-3313T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497613 | |||||||
| chr8:27497622 | T | C | 1 | a0014c0030t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102-3304T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497622 | |||||||
| chr8:27497899 | C | T | 1 | a0001c0002t0002g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.102-3027C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27497899 | |||||||
| chr8:27497948 | TCATTTAC others(13): Show |
T | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.102-2955_102-2936d others(22): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27497948 | ||||||
| chr8:27498051 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.102-2875A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498051 | |||||||
| chr8:27498251 | C | T | 1 | a0004c0010t0001g0264 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.102-2675C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498251 | |||||||
| chr8:27498255 | G | A | 1 | a0001c0005t0002g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.102-2671G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498255 | |||||||
| chr8:27498407 | C | T | 49 | a0001c0001t0001g0245 a0001c0002t0002g0002 a0001c0002t0002g0004 others(46): Show |
62 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.102-2519C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498407 | |||||||
| chr8:27498573 | G | T | 21 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0035 others(18): Show |
28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.102-2353G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498573 | |||||||
| chr8:27498960 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.102-1966G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498960 | |||||||
| chr8:27498974 | T | G | 318 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(315): Show |
371 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(368): Show |
intron_variant | MODIFIER | c.102-1952T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27498974 | |||||||
| chr8:27499188 | A | T | 4 | a0001c0005t0003g0095 a0001c0005t0003g0096 a0001c0005t0003g0097 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1738A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499188 | |||||||
| chr8:27499294 | C | A | 4 | a0001c0002t0002g0216 a0001c0002t0002g0217 a0001c0002t0002g0218 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-1632C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499294 | |||||||
| chr8:27499299 | G | C | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.102-1627G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499299 | |||||||
| chr8:27499322 | A | G | 1 | a0003c0006t0002g0313 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.102-1604A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499322 | |||||||
| chr8:27499502 | T | C | 10 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0003c0007t0004g0280 others(7): Show |
10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.102-1424T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499502 | |||||||
| chr8:27499762 | T | C | 14 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(11): Show |
14 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.102-1164T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499762 | |||||||
| chr8:27499793 | G | A | 1 | a0001c0004t0003g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.102-1133G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499793 | |||||||
| chr8:27499840 | G | GTTC | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.102-1084_102-1082d others(5): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | 27499840 | ||||||
| chr8:27499895 | C | A | 1 | a0019c0026t0002g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.102-1031C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27499895 | |||||||
| chr8:27500177 | C | T | 13 | a0001c0001t0001g0040 a0004c0010t0001g0257 a0004c0010t0001g0258 others(10): Show |
14 | HG00639.hp2 HG00738.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.102-749C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500177 | |||||||
| chr8:27500616 | G | A | 1 | a0003c0007t0008g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102-310G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500616 | |||||||
| chr8:27500768 | C | T | 1 | a0003c0007t0004g0285 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.102-158C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500768 | |||||||
| chr8:27500770 | C | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0027 others(10): Show |
16 | HG00423.hp1 HG01496.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.102-156C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500770 | |||||||
| chr8:27500852 | T | C | 3 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0220 |
5 | NA18946.hp1 NA18954.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-74T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 1/18 | chr8 | 27500852 | |||||||
| chr8:27501124 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.186+114C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501124 | |||||||
| chr8:27501277 | C | T | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.186+267C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501277 | |||||||
| chr8:27501280 | C | T | 1 | a0001c0005t0002g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.186+270C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501280 | |||||||
| chr8:27501324 | T | C | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.186+314T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501324 | |||||||
| chr8:27501324 | T | TTTC | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(38): Show |
41 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.186+383_186+385dup others(3): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | T | TTTCTTC | 26 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
29 | HG00597.hp1 HG00621.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.186+380_186+385dup others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | T | TTTCTTCT others(2): Show |
17 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0115 others(14): Show |
17 | HG00544.hp2 HG00735.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.186+377_186+385dup others(9): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | T | TTTCTTCT others(5): Show |
12 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0117 others(9): Show |
12 | HG01261.hp1 HG02280.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.186+374_186+385dup others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | T | TTTCTTCT others(8): Show |
7 | a0001c0001t0001g0025 a0001c0001t0001g0133 a0001c0001t0001g0141 others(4): Show |
7 | HG01106.hp2 HG02055.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+371_186+385dup others(15): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | T | TTTCTTCT others(11): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02083.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.186+368_186+385dup others(18): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | T | TTTCTTCT others(14): Show |
7 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0124 others(4): Show |
7 | HG02735.hp1 HG02735.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+365_186+385dup others(21): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | TTTC | T | 43 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0110 others(40): Show |
46 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.186+383_186+385del others(3): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | TTTCTTC | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0119 a0001c0001t0001g0152 others(34): Show |
39 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.186+380_186+385del others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | TTTCTTCT others(2): Show |
T | 45 | a0001c0001t0001g0042 a0001c0001t0001g0091 a0001c0001t0001g0101 others(42): Show |
47 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.186+377_186+385del others(9): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | TTTCTTCT others(5): Show |
T | 16 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0114 others(13): Show |
17 | HG00323.hp1 HG00609.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.186+374_186+385del others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | TTTCTTCT others(8): Show |
T | 5 | a0001c0002t0002g0002 a0001c0005t0003g0095 a0001c0031t0001g0147 others(2): Show |
6 | HG00408.hp1 HG00733.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+371_186+385del others(15): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | TTTCTTCT others(11): Show |
T | 3 | a0001c0001t0001g0135 a0001c0002t0002g0222 a0001c0025t0001g0244 |
3 | HG02698.hp1 HG03139.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.186+368_186+385del others(18): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | TTTCTTCT others(14): Show |
T | 3 | a0001c0001t0001g0151 a0001c0002t0002g0002 a0006c0020t0001g0109 |
3 | HG01891.hp1 NA18947.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.186+365_186+385del others(21): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501324 | TTTCTTCT others(17): Show |
T | 1 | a0004c0010t0001g0264 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.186+362_186+385del others(24): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501324 | ||||||
| chr8:27501331 | T | C | 1 | a0001c0005t0006g0102 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.186+321T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501331 | |||||||
| chr8:27501363 | C | T | 1 | a0001c0002t0002g0253 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.186+353C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501363 | |||||||
| chr8:27501380 | T | TC | 5 | a0003c0006t0002g0277 a0003c0006t0002g0303 a0003c0006t0002g0306 others(2): Show |
5 | HG00642.hp1 HG00733.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+371dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501380 | ||||||
| chr8:27501381 | C | CTTTCTTC others(99): Show |
1 | a0001c0001t0001g0188 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.186+373_186+374ins others(106): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501381 | ||||||
| chr8:27501382 | T | TTCTTCTT others(71): Show |
2 | a0001c0013t0002g0045 a0001c0013t0006g0046 |
2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.186+385_186+386ins others(78): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501382 | ||||||
| chr8:27501382 | T | TTCTTCTT others(76): Show |
1 | a0001c0001t0001g0047 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.186+385_186+386ins others(83): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501382 | ||||||
| chr8:27501383 | T | TC | 6 | a0003c0006t0002g0304 a0003c0006t0002g0308 a0003c0006t0002g0312 others(3): Show |
6 | HG01167.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+374dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501383 | ||||||
| chr8:27501387 | C | CCTTCT | 5 | a0003c0006t0002g0277 a0003c0006t0002g0302 a0003c0006t0002g0310 others(2): Show |
5 | HG00733.hp1 HG02257.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+377_186+378ins others(5): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501387 | |||||||
| chr8:27501387 | C | CCTTCTTC others(5): Show |
3 | a0003c0006t0002g0309 a0003c0007t0004g0279 a0003c0007t0004g0283 |
3 | HG02280.hp2 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.186+377_186+378ins others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501387 | |||||||
| chr8:27501387 | C | CT | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0007c0012t0001g0268 others(1): Show |
4 | HG00639.hp1 HG01978.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+379dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | ||||||
| chr8:27501387 | C | CTTCTCCT others(178): Show |
1 | a0001c0001t0001g0104 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.186+381_186+382ins others(185): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | ||||||
| chr8:27501387 | C | CTTCTTCT | 3 | a0001c0001t0001g0192 a0001c0002t0002g0216 a0001c0017t0001g0193 |
3 | HG02886.hp1 NA18951.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.186+401_186+407dup others(7): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | ||||||
| chr8:27501387 | C | CTTCTTCT others(174): Show |
1 | a0001c0001t0001g0105 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.186+384_186+385ins others(181): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | ||||||
| chr8:27501387 | C | CTTCTTCT others(3): Show |
1 | a0001c0001t0001g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.186+385_186+386ins others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | ||||||
| chr8:27501387 | C | CTTCTTCT others(6): Show |
2 | a0001c0005t0003g0301 a0001c0017t0001g0190 |
2 | HG02165.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.186+385_186+386ins others(13): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | ||||||
| chr8:27501387 | C | CTTCTTCT others(9): Show |
3 | a0001c0001t0001g0189 a0007c0012t0001g0265 a0007c0029t0003g0300 |
3 | HG02523.hp1 HG02523.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.186+385_186+386ins others(16): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | ||||||
| chr8:27501387 | C | CTTCTTCT others(179): Show |
1 | a0001c0001t0006g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.186+385_186+386ins others(186): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | ||||||
| chr8:27501387 | C | CTTCTTCT others(99): Show |
1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.186+385_186+386ins others(106): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501387 | ||||||
| chr8:27501389 | T | C | 8 | a0003c0006t0002g0277 a0003c0006t0002g0302 a0003c0006t0002g0309 others(5): Show |
8 | HG00733.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+379T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501389 | |||||||
| chr8:27501389 | T | TC | 6 | a0003c0006t0002g0304 a0003c0006t0002g0308 a0003c0006t0002g0312 others(3): Show |
6 | HG01167.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.186+380dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | ||||||
| chr8:27501389 | T | TCCTTCTT others(8): Show |
4 | a0003c0006t0002g0276 a0003c0007t0004g0280 a0003c0007t0004g0281 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+380_186+381ins others(15): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | ||||||
| chr8:27501389 | T | TCTCCTTC others(199): Show |
1 | a0001c0001t0001g0103 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.186+381_186+382ins others(206): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | ||||||
| chr8:27501389 | T | TCTTCTTC others(14): Show |
1 | a0003c0007t0012g0284 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.186+385_186+386ins others(21): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | ||||||
| chr8:27501389 | T | TCTTCTTC others(17): Show |
1 | a0003c0007t0004g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186+385_186+386ins others(24): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501389 | ||||||
| chr8:27501394 | T | C | 1 | a0003c0006t0002g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186+384T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501394 | |||||||
| chr8:27501394 | T | TGCTTCTG others(100): Show |
1 | a0001c0014t0003g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186+384_186+385ins others(107): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501394 | |||||||
| chr8:27501394 | T | TTCTGCTT others(103): Show |
1 | a0001c0014t0003g0299 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186+385_186+386ins others(110): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501394 | ||||||
| chr8:27501395 | T | TCTTCTTC others(6): Show |
1 | a0001c0002t0002g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.186+385_186+386ins others(13): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501395 | |||||||
| chr8:27501396 | T | C | 23 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(20): Show |
23 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.186+386T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501396 | |||||||
| chr8:27501401 | T | C | 1 | a0003c0006t0002g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186+391T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501401 | |||||||
| chr8:27501403 | T | C | 8 | a0003c0006t0002g0302 a0003c0006t0002g0305 a0003c0006t0002g0308 others(5): Show |
8 | HG01106.hp1 HG01167.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.186+393T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501403 | |||||||
| chr8:27501410 | T | C | 1 | a0003c0006t0002g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186+400T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501410 | |||||||
| chr8:27501411 | C | CTTCT | 21 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(18): Show |
21 | HG00733.hp1 HG01106.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.186+404_186+407dup others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501411 | ||||||
| chr8:27501411 | C | T | 1 | a0003c0006t0002g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186+401C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501411 | |||||||
| chr8:27501418 | T | C | 2 | a0001c0014t0003g0298 a0001c0014t0003g0299 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.186+408T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501418 | |||||||
| chr8:27501420 | C | T | 2 | a0001c0014t0003g0298 a0001c0014t0003g0299 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.186+410C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501420 | |||||||
| chr8:27501421 | T | C | 3 | a0001c0001t0001g0107 a0001c0014t0003g0298 a0001c0014t0003g0299 |
3 | HG01243.hp2 NA18522.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.186+411T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501421 | |||||||
| chr8:27501613 | G | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.186+603G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501613 | |||||||
| chr8:27501654 | A | T | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.186+644A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501654 | |||||||
| chr8:27501776 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.186+766G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501776 | |||||||
| chr8:27501849 | A | G | 1 | a0001c0014t0003g0297 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186+839A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501849 | |||||||
| chr8:27501869 | T | C | 1 | a0015c0036t0002g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.186+859T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501869 | |||||||
| chr8:27501906 | TA | T | 16 | a0001c0004t0004g0296 a0001c0005t0002g0017 a0001c0005t0002g0092 others(13): Show |
18 | HG00597.hp2 HG00621.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.186+906delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr8 | 27501906 | ||||||
| chr8:27501978 | A | C | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.186+968A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27501978 | |||||||
| chr8:27502084 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.186+1074C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502084 | |||||||
| chr8:27502090 | C | G | 2 | a0004c0010t0001g0263 a0004c0010t0001g0264 |
2 | HG00639.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.186+1080C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502090 | |||||||
| chr8:27502103 | C | T | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.186+1093C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502103 | |||||||
| chr8:27502197 | C | T | 1 | a0003c0006t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.186+1187C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502197 | |||||||
| chr8:27502239 | A | G | 8 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(5): Show |
9 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.186+1229A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502239 | |||||||
| chr8:27502247 | C | T | 2 | a0002c0003t0003g0207 a0002c0003t0003g0208 |
2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.186+1237C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502247 | |||||||
| chr8:27502268 | A | G | 1 | a0003c0007t0004g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186+1258A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502268 | |||||||
| chr8:27502455 | T | C | 21 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0035 others(18): Show |
28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.187-1149T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502455 | |||||||
| chr8:27502896 | G | A | 1 | a0006c0020t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187-708G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502896 | |||||||
| chr8:27502972 | C | T | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.187-632C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27502972 | |||||||
| chr8:27503051 | G | T | 21 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0035 others(18): Show |
28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.187-553G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503051 | |||||||
| chr8:27503073 | G | A | 2 | a0004c0015t0004g0254 a0004c0015t0004g0255 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.187-531G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503073 | |||||||
| chr8:27503147 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.187-457G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503147 | |||||||
| chr8:27503283 | T | G | 1 | a0019c0026t0002g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.187-321T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503283 | |||||||
| chr8:27503404 | G | T | 1 | a0001c0001t0006g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.187-200G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503404 | |||||||
| chr8:27503448 | A | C | 21 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0035 others(18): Show |
28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.187-156A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503448 | |||||||
| chr8:27503530 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.187-74G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 2/18 | chr8 | 27503530 | |||||||
| chr8:27503794 | C | T | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.346+31C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503794 | |||||||
| chr8:27503812 | C | T | 13 | a0001c0001t0001g0040 a0004c0010t0001g0257 a0004c0010t0001g0258 others(10): Show |
14 | HG00639.hp2 HG00738.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.346+49C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503812 | |||||||
| chr8:27503835 | T | C | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.346+72T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503835 | |||||||
| chr8:27503872 | C | T | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.346+109C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503872 | |||||||
| chr8:27503873 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.346+110G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503873 | |||||||
| chr8:27503899 | C | A | 2 | a0003c0006t0002g0276 a0003c0006t0002g0277 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.346+136C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503899 | |||||||
| chr8:27503998 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.346+235T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27503998 | |||||||
| chr8:27504117 | G | T | 1 | a0007c0012t0001g0265 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.346+354G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27504117 | |||||||
| chr8:27504245 | A | AC | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.346+482_346+483ins others(1): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27504245 | |||||||
| chr8:27504625 | T | C | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.347-331T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 3/18 | chr8 | 27504625 | |||||||
| chr8:27505171 | G | C | 21 | a0001c0004t0003g0010 a0001c0004t0003g0011 a0001c0004t0003g0035 others(18): Show |
28 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.537+25G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505171 | |||||||
| chr8:27505269 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | NA18954.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.537+123C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505269 | |||||||
| chr8:27505368 | A | C | 4 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(1): Show |
6 | HG02055.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+222A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505368 | |||||||
| chr8:27505512 | C | T | 1 | a0003c0006t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.537+366C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505512 | |||||||
| chr8:27505601 | G | A | 2 | a0002c0011t0001g0201 a0002c0011t0001g0202 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.537+455G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505601 | |||||||
| chr8:27505619 | A | G | 100 | a0001c0001t0001g0047 a0001c0001t0001g0245 a0001c0002t0002g0002 others(97): Show |
120 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.537+473A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505619 | |||||||
| chr8:27505630 | T | C | 1 | a0001c0002t0002g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.537+484T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505630 | |||||||
| chr8:27505721 | G | C | 2 | a0005c0009t0001g0087 a0005c0009t0001g0088 |
2 | HG02129.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.537+575G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505721 | |||||||
| chr8:27505874 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.537+728A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505874 | |||||||
| chr8:27505922 | A | G | 1 | a0001c0002t0002g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.537+776A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27505922 | |||||||
| chr8:27506051 | C | T | 10 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0003c0007t0004g0280 others(7): Show |
10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.538-821C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506051 | |||||||
| chr8:27506096 | G | C | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.538-776G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506096 | |||||||
| chr8:27506107 | G | A | 43 | a0001c0001t0001g0245 a0001c0002t0002g0002 a0001c0002t0002g0004 others(40): Show |
56 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.538-765G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506107 | |||||||
| chr8:27506330 | T | C | 1 | a0001c0001t0001g0006 | 3 | NA18960.hp1 NA18966.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.538-542T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506330 | |||||||
| chr8:27506353 | G | T | 1 | a0004c0010t0001g0262 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.538-519G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506353 | |||||||
| chr8:27506795 | T | C | 1 | a0003c0035t0001g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.538-77T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 4/18 | chr8 | 27506795 | |||||||
| chr8:27507270 | T | C | 284 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
335 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(332): Show |
intron_variant | MODIFIER | c.660+276T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507270 | |||||||
| chr8:27507358 | G | C | 1 | a0003c0007t0004g0282 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.660+364G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507358 | |||||||
| chr8:27507422 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.660+428C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507422 | |||||||
| chr8:27507440 | G | A | 53 | a0001c0001t0001g0245 a0001c0002t0002g0002 a0001c0002t0002g0004 others(50): Show |
66 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.660+446G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507440 | |||||||
| chr8:27507447 | A | G | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+453A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507447 | |||||||
| chr8:27507449 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.660+455C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507449 | |||||||
| chr8:27507471 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.660+477G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507471 | |||||||
| chr8:27507532 | G | A | 9 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0220 others(6): Show |
11 | HG00438.hp1 HG03927.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.660+538G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507532 | |||||||
| chr8:27507639 | A | G | 12 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(9): Show |
12 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.660+645A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507639 | |||||||
| chr8:27507695 | T | A | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.660+701T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507695 | |||||||
| chr8:27507751 | A | C | 40 | a0001c0001t0001g0245 a0001c0002t0002g0002 a0001c0002t0002g0004 others(37): Show |
53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.660+757A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507751 | |||||||
| chr8:27507897 | C | T | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+903C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507897 | |||||||
| chr8:27507913 | C | A | 125 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0245 others(122): Show |
147 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.660+919C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507913 | |||||||
| chr8:27507985 | G | A | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+991G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27507985 | |||||||
| chr8:27508013 | G | A | 1 | a0002c0003t0003g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.660+1019G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508013 | |||||||
| chr8:27508131 | G | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.660+1137G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508131 | |||||||
| chr8:27508195 | C | T | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.660+1201C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508195 | |||||||
| chr8:27508306 | A | AAAAC | 50 | a0001c0001t0001g0047 a0001c0004t0003g0010 a0001c0004t0003g0011 others(47): Show |
57 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.660+1324_660+1327d others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508306 | ||||||
| chr8:27508329 | T | G | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.660+1335T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508329 | |||||||
| chr8:27508371 | T | C | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+1377T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508371 | |||||||
| chr8:27508635 | T | G | 14 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(11): Show |
14 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.660+1641T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508635 | |||||||
| chr8:27508659 | G | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.660+1665G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508659 | |||||||
| chr8:27508668 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.660+1674G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508668 | |||||||
| chr8:27508699 | C | T | 1 | a0003c0006t0002g0304 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.660+1705C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508699 | |||||||
| chr8:27508735 | C | T | 2 | a0001c0013t0002g0045 a0001c0013t0006g0046 |
2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.660+1741C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508735 | |||||||
| chr8:27508769 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.660+1775C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508769 | |||||||
| chr8:27508770 | G | A | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+1776G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508770 | |||||||
| chr8:27508783 | T | C | 1 | a0003c0006t0002g0309 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.660+1789T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508783 | |||||||
| chr8:27508814 | G | C | 1 | a0001c0014t0003g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.660+1820G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508814 | |||||||
| chr8:27508819 | C | T | 50 | a0001c0001t0001g0047 a0001c0004t0003g0010 a0001c0004t0003g0011 others(47): Show |
57 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.660+1825C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508819 | |||||||
| chr8:27508884 | G | C | 175 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0245 others(172): Show |
210 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.660+1890G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508884 | |||||||
| chr8:27508890 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+1896C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27508890 | |||||||
| chr8:27508946 | C | CT | 62 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0047 others(59): Show |
65 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.660+1979dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | ||||||
| chr8:27508946 | C | CTT | 6 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0002c0011t0001g0202 others(3): Show |
6 | HG01361.hp1 HG01517.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.660+1978_660+1979d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | ||||||
| chr8:27508946 | C | CTTT | 7 | a0001c0013t0006g0046 a0003c0006t0002g0276 a0003c0006t0002g0277 others(4): Show |
7 | HG00733.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+1977_660+1979d others(5): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | ||||||
| chr8:27508946 | CT | C | 22 | a0001c0001t0001g0114 a0001c0002t0002g0034 a0001c0002t0002g0227 others(19): Show |
29 | HG00438.hp1 HG00609.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.660+1979delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | ||||||
| chr8:27508946 | CTT | C | 46 | a0001c0001t0001g0245 a0001c0002t0002g0002 a0001c0002t0002g0004 others(43): Show |
58 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.660+1978_660+1979d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr8 | 27508946 | ||||||
| chr8:27509020 | G | A | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.660+2026G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509020 | |||||||
| chr8:27509215 | G | T | 1 | a0003c0035t0001g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.660+2221G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509215 | |||||||
| chr8:27509399 | G | A | 10 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0003c0007t0004g0280 others(7): Show |
10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.660+2405G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509399 | |||||||
| chr8:27509452 | A | G | 10 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0003c0007t0004g0280 others(7): Show |
10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-2384A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509452 | |||||||
| chr8:27509576 | T | C | 4 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(1): Show |
7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.661-2260T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509576 | |||||||
| chr8:27509623 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.661-2213C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509623 | |||||||
| chr8:27509638 | C | G | 7 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(4): Show |
9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.661-2198C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509638 | |||||||
| chr8:27509659 | G | A | 1 | a0002c0003t0003g0274 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.661-2177G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509659 | |||||||
| chr8:27509755 | A | G | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.661-2081A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509755 | |||||||
| chr8:27509792 | G | C | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-2044G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509792 | |||||||
| chr8:27509972 | G | A | 1 | a0004c0010t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.661-1864G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509972 | |||||||
| chr8:27509984 | A | G | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-1852A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509984 | |||||||
| chr8:27509998 | G | A | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.661-1838G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27509998 | |||||||
| chr8:27510010 | G | C | 2 | a0001c0014t0003g0298 a0001c0014t0003g0299 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.661-1826G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510010 | |||||||
| chr8:27510085 | A | C | 52 | a0001c0001t0001g0245 a0001c0002t0002g0002 a0001c0002t0002g0004 others(49): Show |
65 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.661-1751A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510085 | |||||||
| chr8:27510124 | T | G | 24 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(21): Show |
24 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.661-1712T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510124 | |||||||
| chr8:27510147 | A | G | 10 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0003c0007t0004g0280 others(7): Show |
10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-1689A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510147 | |||||||
| chr8:27510224 | G | A | 9 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(6): Show |
10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-1612G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510224 | |||||||
| chr8:27510257 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.661-1579A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510257 | |||||||
| chr8:27510289 | G | A | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.661-1547G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510289 | |||||||
| chr8:27510322 | G | A | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-1514G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510322 | |||||||
| chr8:27510339 | C | G | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.661-1497C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510339 | |||||||
| chr8:27510560 | T | A | 1 | a0002c0008t0002g0058 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.661-1276T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510560 | |||||||
| chr8:27510766 | C | T | 5 | a0003c0006t0002g0305 a0003c0006t0002g0306 a0003c0006t0002g0308 others(2): Show |
5 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-1070C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510766 | |||||||
| chr8:27510770 | A | G | 4 | a0001c0005t0003g0095 a0001c0005t0003g0096 a0001c0005t0003g0097 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-1066A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510770 | |||||||
| chr8:27510851 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.661-985A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510851 | |||||||
| chr8:27510857 | G | A | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.661-979G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27510857 | |||||||
| chr8:27511061 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.661-775G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511061 | |||||||
| chr8:27511118 | C | T | 3 | a0001c0001t0001g0047 a0001c0013t0002g0045 a0001c0013t0006g0046 |
3 | HG04115.hp1 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.661-718C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511118 | |||||||
| chr8:27511228 | C | T | 1 | a0003c0007t0004g0281 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.661-608C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511228 | |||||||
| chr8:27511251 | G | A | 26 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-585G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511251 | |||||||
| chr8:27511323 | G | A | 1 | a0002c0003t0005g0059 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.661-513G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511323 | |||||||
| chr8:27511488 | A | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | NA18989.hp1 NA19000.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.661-348A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511488 | |||||||
| chr8:27511674 | T | C | 10 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0003c0007t0004g0280 others(7): Show |
10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-162T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511674 | |||||||
| chr8:27511817 | A | G | 231 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(228): Show |
274 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.661-19A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 5/18 | chr8 | 27511817 | |||||||
| chr8:27512065 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.735+155T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512065 | |||||||
| chr8:27512100 | G | GA | 51 | a0001c0001t0001g0108 a0001c0001t0001g0182 a0001c0001t0001g0245 others(48): Show |
64 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.735+208dupA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27512100 | ||||||
| chr8:27512100 | G | GAA | 6 | a0001c0001t0001g0047 a0001c0002t0002g0217 a0001c0002t0002g0228 others(3): Show |
6 | HG01515.hp1 HG01517.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.735+207_735+208dup others(2): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27512100 | ||||||
| chr8:27512216 | G | T | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.735+306G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512216 | |||||||
| chr8:27512272 | C | A | 1 | a0004c0010t0001g0262 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.735+362C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512272 | |||||||
| chr8:27512556 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.735+646C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512556 | |||||||
| chr8:27512572 | C | G | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.735+662C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512572 | |||||||
| chr8:27512785 | T | TTGGACAA others(324): Show |
1 | a0001c0002t0002g0217 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.735+889_735+890ins others(331): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27512785 | ||||||
| chr8:27512804 | C | T | 14 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(11): Show |
14 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.735+894C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512804 | |||||||
| chr8:27512829 | C | T | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.735+919C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27512829 | |||||||
| chr8:27513058 | C | T | 1 | a0003c0007t0008g0273 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.735+1148C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513058 | |||||||
| chr8:27513091 | G | A | 1 | a0003c0006t0002g0309 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.735+1181G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513091 | |||||||
| chr8:27513221 | T | G | 9 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(6): Show |
10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.735+1311T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513221 | |||||||
| chr8:27513261 | G | A | 1 | a0002c0003t0003g0028 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.735+1351G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513261 | |||||||
| chr8:27513323 | T | C | 10 | a0002c0003t0003g0080 a0002c0008t0002g0013 a0002c0008t0002g0057 others(7): Show |
11 | HG01928.hp2 NA18942.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+1413T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513323 | |||||||
| chr8:27513406 | G | T | 5 | a0003c0007t0004g0282 a0003c0007t0004g0283 a0003c0007t0004g0285 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+1496G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513406 | |||||||
| chr8:27513544 | A | C | 1 | a0001c0005t0003g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.735+1634A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513544 | |||||||
| chr8:27513566 | C | T | 4 | a0002c0003t0003g0052 a0002c0003t0003g0053 a0002c0003t0003g0054 others(1): Show |
4 | NA18952.hp1 NA19062.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+1656C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513566 | |||||||
| chr8:27513599 | C | T | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.735+1689C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513599 | |||||||
| chr8:27513655 | C | G | 2 | a0004c0015t0004g0254 a0004c0015t0004g0255 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.735+1745C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513655 | |||||||
| chr8:27513684 | A | T | 3 | a0001c0002t0002g0004 a0001c0002t0002g0246 a0001c0002t0002g0250 |
6 | NA18949.hp2 NA18956.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+1774A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513684 | |||||||
| chr8:27513829 | G | C | 10 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0003c0007t0004g0280 others(7): Show |
10 | HG00733.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.736-1889G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513829 | |||||||
| chr8:27513923 | A | G | 3 | a0001c0004t0003g0039 a0001c0004t0003g0294 a0001c0032t0003g0039 |
3 | HG02258.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.736-1795A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513923 | |||||||
| chr8:27513933 | C | G | 1 | a0001c0002t0002g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.736-1785C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27513933 | |||||||
| chr8:27514029 | T | C | 115 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0245 others(112): Show |
136 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.736-1689T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514029 | |||||||
| chr8:27514030 | C | T | 1 | a0003c0035t0001g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.736-1688C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514030 | |||||||
| chr8:27514060 | G | A | 65 | a0001c0001t0001g0040 a0001c0001t0001g0245 a0001c0002t0002g0002 others(62): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.736-1658G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514060 | |||||||
| chr8:27514091 | G | A | 65 | a0001c0001t0001g0040 a0001c0001t0001g0245 a0001c0002t0002g0002 others(62): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.736-1627G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514091 | |||||||
| chr8:27514095 | A | G | 65 | a0001c0001t0001g0040 a0001c0001t0001g0245 a0001c0002t0002g0002 others(62): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.736-1623A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514095 | |||||||
| chr8:27514142 | A | AC | 10 | a0001c0001t0001g0211 a0001c0005t0002g0017 a0001c0005t0002g0092 others(7): Show |
11 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.736-1570dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27514142 | ||||||
| chr8:27514167 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.736-1551G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514167 | |||||||
| chr8:27514222 | G | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.736-1496G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514222 | |||||||
| chr8:27514222 | G | T | 1 | a0001c0001t0001g0156 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.736-1496G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514222 | |||||||
| chr8:27514251 | G | A | 1 | a0002c0003t0003g0063 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.736-1467G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514251 | |||||||
| chr8:27514302 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0132 |
2 | NA18961.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.736-1416G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514302 | |||||||
| chr8:27514309 | A | G | 2 | a0001c0014t0003g0298 a0001c0014t0003g0299 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.736-1409A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514309 | |||||||
| chr8:27514412 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.736-1306A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514412 | |||||||
| chr8:27514629 | T | C | 2 | a0001c0002t0002g0203 a0001c0002t0002g0204 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.736-1089T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514629 | |||||||
| chr8:27514672 | G | A | 114 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0245 others(111): Show |
135 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.736-1046G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514672 | |||||||
| chr8:27514694 | A | G | 2 | a0001c0013t0002g0045 a0001c0013t0006g0046 |
2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.736-1024A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514694 | |||||||
| chr8:27514718 | C | T | 2 | a0003c0006t0002g0276 a0003c0006t0002g0277 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.736-1000C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27514718 | |||||||
| chr8:27515143 | G | A | 14 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(11): Show |
19 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.736-575G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515143 | |||||||
| chr8:27515189 | TC | T | 16 | a0001c0001t0001g0040 a0003c0006t0002g0309 a0003c0007t0004g0278 others(13): Show |
17 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.736-525delC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27515189 | ||||||
| chr8:27515194 | G | GT | 4 | a0001c0001t0001g0189 a0001c0002t0002g0220 a0001c0002t0002g0227 others(1): Show |
4 | HG00438.hp1 NA18941.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-517dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27515194 | ||||||
| chr8:27515201 | T | C | 16 | a0001c0001t0001g0040 a0003c0006t0002g0309 a0003c0007t0004g0278 others(13): Show |
17 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.736-517T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515201 | |||||||
| chr8:27515479 | AT | A | 14 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(11): Show |
19 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.736-238delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515479 | |||||||
| chr8:27515535 | TAGGTTGG others(15): Show |
T | 2 | a0002c0003t0003g0207 a0002c0003t0003g0208 |
2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.736-180_736-159del others(22): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr8 | 27515535 | ||||||
| chr8:27515568 | A | C | 2 | a0002c0003t0003g0205 a0002c0003t0003g0206 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.736-150A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515568 | |||||||
| chr8:27515652 | G | A | 3 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 |
3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.736-66G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515652 | |||||||
| chr8:27515689 | C | A | 1 | a0019c0026t0002g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.736-29C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 6/18 | chr8 | 27515689 | |||||||
| chr8:27515892 | G | A | 5 | a0001c0002t0002g0031 a0001c0002t0002g0234 a0001c0002t0002g0235 others(2): Show |
6 | HG00423.hp2 HG02040.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+79G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27515892 | |||||||
| chr8:27515960 | A | T | 1 | a0002c0008t0002g0058 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.831+147A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27515960 | |||||||
| chr8:27515963 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0129 |
5 | HG01074.hp1 HG01257.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+150C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27515963 | |||||||
| chr8:27516051 | G | A | 1 | a0003c0007t0004g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.831+238G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27516051 | |||||||
| chr8:27516191 | T | A | 1 | a0003c0006t0002g0310 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.832-129T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 7/18 | chr8 | 27516191 | |||||||
| chr8:27516406 | T | C | 113 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(110): Show |
134 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(131): Show |
splice_region_variant&intron_variant | LOW | c.910+8T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516406 | |||||||
| chr8:27516410 | GTCTTGCA others(17): Show |
G | 1 | a0001c0002t0002g0220 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.910+14_910+37delCT others(22): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516410 | ||||||
| chr8:27516462 | C | T | 7 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(4): Show |
10 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.910+64C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516462 | |||||||
| chr8:27516547 | C | T | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
8 | HG02083.hp2 NA18939.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+149C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516547 | |||||||
| chr8:27516663 | A | G | 1 | a0004c0010t0001g0262 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.910+265A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516663 | |||||||
| chr8:27516665 | A | G | 1 | a0001c0005t0002g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.910+267A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516665 | |||||||
| chr8:27516884 | C | T | 9 | a0001c0001t0001g0040 a0004c0010t0001g0257 a0004c0010t0001g0258 others(6): Show |
10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.910+486C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516884 | |||||||
| chr8:27516892 | T | G | 8 | a0003c0007t0004g0280 a0003c0007t0004g0281 a0003c0007t0004g0282 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.910+494T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516892 | |||||||
| chr8:27516917 | C | CTT | 26 | a0001c0002t0002g0029 a0001c0002t0002g0223 a0001c0002t0002g0246 others(23): Show |
32 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.910+520_910+521ins others(2): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516917 | ||||||
| chr8:27516917 | C | CTTT | 49 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(46): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.910+520_910+521ins others(3): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516917 | ||||||
| chr8:27516917 | C | CTTTT | 5 | a0001c0002t0002g0228 a0001c0002t0002g0229 a0001c0013t0002g0045 others(2): Show |
5 | HG01515.hp1 HG01517.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+520_910+521ins others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516917 | ||||||
| chr8:27516919 | A | AT | 27 | a0001c0001t0001g0040 a0001c0001t0001g0154 a0001c0001t0001g0155 others(24): Show |
29 | HG00639.hp2 HG01192.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.910+539dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516919 | ||||||
| chr8:27516919 | A | T | 80 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(77): Show |
98 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.910+521A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27516919 | |||||||
| chr8:27516919 | AT | A | 10 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0130 others(7): Show |
10 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.910+539delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27516919 | ||||||
| chr8:27517063 | G | A | 1 | a0001c0005t0003g0095 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.910+665G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517063 | |||||||
| chr8:27517169 | A | T | 42 | a0001c0005t0003g0071 a0002c0003t0002g0070 a0002c0003t0002g0083 others(39): Show |
54 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.910+771A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517169 | |||||||
| chr8:27517200 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG00738.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.910+802T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517200 | |||||||
| chr8:27517282 | ACTACCCA others(3): Show |
A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.911-755_911-746del others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517282 | |||||||
| chr8:27517315 | A | G | 2 | a0004c0015t0004g0254 a0004c0015t0004g0255 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.911-723A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517315 | |||||||
| chr8:27517381 | C | G | 3 | a0001c0004t0004g0290 a0001c0004t0004g0291 a0001c0004t0004g0292 |
3 | HG02258.hp2 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.911-657C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517381 | |||||||
| chr8:27517409 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.911-629C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517409 | |||||||
| chr8:27517418 | G | A | 7 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(4): Show |
9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.911-620G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517418 | |||||||
| chr8:27517636 | C | T | 3 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 |
3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.911-402C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517636 | |||||||
| chr8:27517795 | CAG | C | 8 | a0003c0007t0004g0280 a0003c0007t0004g0281 a0003c0007t0004g0282 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.911-242_911-241del others(2): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517795 | |||||||
| chr8:27517886 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.911-152G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | chr8 | 27517886 | |||||||
| chr8:27517928 | TTTG | T | 4 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(1): Show |
6 | HG02055.hp2 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.911-98_911-96delGT others(1): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr8 | 27517928 | ||||||
| chr8:27518189 | A | T | 7 | a0003c0006t0002g0309 a0003c0007t0004g0278 a0003c0007t0004g0279 others(4): Show |
7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.945+117A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518189 | |||||||
| chr8:27518232 | C | T | 1 | a0003c0006t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.945+160C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518232 | |||||||
| chr8:27518323 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.945+251G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518323 | |||||||
| chr8:27518343 | C | T | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.945+271C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518343 | |||||||
| chr8:27518382 | C | T | 7 | a0003c0006t0002g0309 a0003c0007t0004g0278 a0003c0007t0004g0279 others(4): Show |
7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.945+310C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518382 | |||||||
| chr8:27518462 | T | C | 9 | a0001c0001t0001g0040 a0004c0010t0001g0257 a0004c0010t0001g0258 others(6): Show |
10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.945+390T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518462 | |||||||
| chr8:27518726 | T | C | 3 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 |
3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.945+654T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518726 | |||||||
| chr8:27518787 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0141 |
3 | NA18981.hp1 NA18992.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.945+715T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27518787 | |||||||
| chr8:27519002 | T | C | 2 | a0003c0007t0004g0278 a0003c0007t0004g0279 |
2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.945+930T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519002 | |||||||
| chr8:27519125 | A | G | 1 | a0001c0002t0002g0225 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.945+1053A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519125 | |||||||
| chr8:27519133 | G | A | 1 | a0001c0013t0002g0045 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.945+1061G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519133 | |||||||
| chr8:27519338 | C | T | 2 | a0003c0007t0004g0278 a0003c0007t0004g0279 |
2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.945+1266C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519338 | |||||||
| chr8:27519440 | C | T | 2 | a0001c0002t0002g0222 a0001c0025t0001g0244 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.945+1368C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519440 | |||||||
| chr8:27519631 | TG | T | 3 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0209 |
3 | HG02896.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.946-1251delG | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519631 | |||||||
| chr8:27519645 | C | T | 51 | a0001c0001t0001g0113 a0001c0002t0002g0002 a0001c0002t0002g0004 others(48): Show |
64 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.946-1238C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519645 | |||||||
| chr8:27519646 | G | T | 1 | a0003c0006t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.946-1237G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519646 | |||||||
| chr8:27519716 | C | T | 1 | a0005c0009t0001g0088 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.946-1167C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519716 | |||||||
| chr8:27519772 | C | T | 1 | a0001c0002t0002g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.946-1111C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519772 | |||||||
| chr8:27519819 | A | C | 3 | a0003c0007t0004g0282 a0003c0007t0004g0283 a0003c0007t0004g0285 |
3 | HG02559.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.946-1064A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519819 | |||||||
| chr8:27519837 | A | G | 1 | a0001c0004t0004g0290 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.946-1046A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519837 | |||||||
| chr8:27519972 | G | A | 2 | a0004c0015t0004g0254 a0004c0015t0004g0255 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.946-911G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27519972 | |||||||
| chr8:27520005 | T | C | 1 | a0001c0002t0002g0220 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.946-878T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520005 | |||||||
| chr8:27520006 | C | CT | 17 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(14): Show |
20 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.946-863dupT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr8 | 27520006 | ||||||
| chr8:27520006 | C | T | 1 | a0001c0002t0002g0220 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.946-877C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520006 | |||||||
| chr8:27520021 | A | G | 1 | a0003c0035t0001g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.946-862A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520021 | |||||||
| chr8:27520119 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.946-764G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520119 | |||||||
| chr8:27520160 | T | A | 1 | a0001c0002t0002g0220 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.946-723T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520160 | |||||||
| chr8:27520162 | A | T | 1 | a0001c0002t0002g0220 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.946-721A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520162 | |||||||
| chr8:27520228 | C | A | 1 | a0001c0001t0001g0041 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.946-655C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520228 | |||||||
| chr8:27520286 | C | T | 17 | a0001c0001t0001g0040 a0003c0007t0004g0280 a0003c0007t0004g0281 others(14): Show |
18 | HG00639.hp2 HG01192.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.946-597C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520286 | |||||||
| chr8:27520365 | T | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.946-518T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520365 | |||||||
| chr8:27520427 | A | G | 1 | a0001c0002t0002g0217 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.946-456A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520427 | |||||||
| chr8:27520440 | G | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.946-443G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520440 | |||||||
| chr8:27520492 | G | A | 2 | a0004c0015t0004g0254 a0004c0015t0004g0255 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.946-391G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520492 | |||||||
| chr8:27520584 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.946-299T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520584 | |||||||
| chr8:27520592 | G | A | 1 | a0004c0010t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.946-291G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520592 | |||||||
| chr8:27520629 | G | T | 14 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(11): Show |
19 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.946-254G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520629 | |||||||
| chr8:27520640 | C | T | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.946-243C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520640 | |||||||
| chr8:27520641 | G | A | 1 | a0001c0014t0003g0297 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.946-242G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520641 | |||||||
| chr8:27520658 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0180 |
2 | HG02027.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.946-225T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520658 | |||||||
| chr8:27520742 | T | A | 3 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 |
3 | HG02027.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.946-141T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520742 | |||||||
| chr8:27520878 | C | T | 5 | a0003c0007t0004g0282 a0003c0007t0004g0283 a0003c0007t0004g0285 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.946-5C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 9/18 | chr8 | 27520878 | |||||||
| chr8:27520986 | C | T | 7 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(4): Show |
9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.972+77C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27520986 | |||||||
| chr8:27521000 | C | T | 2 | a0004c0010t0001g0263 a0004c0010t0001g0264 |
2 | HG00639.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.972+91C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521000 | |||||||
| chr8:27521032 | G | C | 2 | a0003c0006t0002g0276 a0003c0006t0002g0277 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.972+123G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521032 | |||||||
| chr8:27521087 | T | G | 4 | a0001c0005t0003g0095 a0001c0005t0003g0096 a0001c0005t0003g0097 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.972+178T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521087 | |||||||
| chr8:27521101 | G | T | 1 | a0001c0002t0002g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.972+192G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521101 | |||||||
| chr8:27521116 | T | C | 131 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(128): Show |
154 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.972+207T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521116 | |||||||
| chr8:27521213 | G | A | 1 | a0003c0007t0004g0278 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.972+304G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521213 | |||||||
| chr8:27521400 | G | A | 16 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(13): Show |
21 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.972+491G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521400 | |||||||
| chr8:27521515 | C | T | 1 | a0001c0005t0005g0215 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.972+606C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521515 | |||||||
| chr8:27521606 | C | A | 1 | a0002c0003t0003g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.972+697C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521606 | |||||||
| chr8:27521797 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.973-626G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521797 | |||||||
| chr8:27521804 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.973-619G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521804 | |||||||
| chr8:27521812 | C | T | 4 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(1): Show |
7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.973-611C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521812 | |||||||
| chr8:27521813 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0129 |
3 | HG01257.hp2 HG01361.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.973-610G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521813 | |||||||
| chr8:27521949 | G | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.973-474G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521949 | |||||||
| chr8:27521972 | C | T | 1 | a0001c0002t0002g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.973-451C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27521972 | |||||||
| chr8:27522082 | G | T | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.973-341G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27522082 | |||||||
| chr8:27522140 | A | AAGG | 244 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(241): Show |
287 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.973-281_973-280ins others(3): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr8 | 27522140 | ||||||
| chr8:27522303 | G | C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-120G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27522303 | |||||||
| chr8:27522304 | A | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-119A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 10/18 | chr8 | 27522304 | |||||||
| chr8:27522646 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1058+138A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522646 | |||||||
| chr8:27522681 | G | A | 1 | a0002c0003t0003g0074 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1058+173G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522681 | |||||||
| chr8:27522750 | A | G | 10 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1058+242A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522750 | |||||||
| chr8:27522845 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1058+337C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522845 | |||||||
| chr8:27522876 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0142 others(1): Show |
4 | HG01109.hp2 HG02602.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+368G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522876 | |||||||
| chr8:27522942 | C | T | 4 | a0001c0002t0002g0216 a0001c0002t0002g0217 a0001c0002t0002g0218 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+434C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27522942 | |||||||
| chr8:27522962 | C | CA | 27 | a0001c0001t0001g0047 a0001c0001t0001g0103 a0001c0001t0001g0105 others(24): Show |
27 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1058+479dupA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27522962 | ||||||
| chr8:27522962 | CA | C | 27 | a0001c0001t0001g0023 a0001c0001t0001g0165 a0001c0001t0001g0173 others(24): Show |
30 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1058+479delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27522962 | ||||||
| chr8:27522962 | CAA | C | 75 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(72): Show |
93 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.1058+478_1058+479d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27522962 | ||||||
| chr8:27522962 | CAAA | C | 14 | a0001c0001t0001g0040 a0001c0002t0002g0229 a0001c0002t0002g0243 others(11): Show |
16 | HG00639.hp2 HG01192.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1058+477_1058+479d others(5): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27522962 | ||||||
| chr8:27523036 | G | T | 3 | a0001c0002t0002g0004 a0001c0002t0002g0246 a0001c0002t0002g0250 |
6 | NA18949.hp2 NA18956.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058+528G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523036 | |||||||
| chr8:27523078 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1058+570A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523078 | |||||||
| chr8:27523246 | G | A | 5 | a0007c0012t0001g0265 a0007c0012t0001g0266 a0007c0012t0001g0268 others(2): Show |
5 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+738G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523246 | |||||||
| chr8:27523414 | C | T | 2 | a0003c0007t0004g0281 a0003c0007t0004g0287 |
2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1058+906C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523414 | |||||||
| chr8:27523650 | T | C | 9 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(6): Show |
10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1058+1142T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523650 | |||||||
| chr8:27523677 | G | C | 122 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(119): Show |
144 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.1058+1169G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523677 | |||||||
| chr8:27523690 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1058+1182C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523690 | |||||||
| chr8:27523715 | T | A | 7 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(4): Show |
9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1058+1207T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523715 | |||||||
| chr8:27523762 | C | G | 3 | a0001c0004t0003g0010 a0001c0004t0003g0288 a0013c0037t0004g0044 |
5 | HG02145.hp1 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+1254C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523762 | |||||||
| chr8:27523874 | C | T | 2 | a0009c0018t0001g0267 a0009c0018t0001g0269 |
2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1058+1366C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27523874 | |||||||
| chr8:27523935 | GT | G | 107 | a0001c0001t0001g0113 a0001c0001t0001g0148 a0001c0001t0001g0150 others(104): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1059-1412delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27523935 | ||||||
| chr8:27523935 | GTT | G | 10 | a0001c0001t0001g0040 a0003c0006t0002g0309 a0004c0010t0001g0257 others(7): Show |
11 | HG00639.hp2 HG01192.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1059-1413_1059-141 others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27523935 | ||||||
| chr8:27523955 | CAG | C | 3 | a0003c0007t0004g0280 a0003c0007t0004g0281 a0003c0007t0004g0287 |
3 | HG02615.hp1 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1059-1404_1059-140 others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27523955 | ||||||
| chr8:27524125 | G | A | 1 | a0001c0002t0002g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1059-1237G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524125 | |||||||
| chr8:27524241 | TATTCCTT others(8): Show |
T | 59 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(56): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1059-1118_1059-110 others(19): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27524241 | ||||||
| chr8:27524379 | G | C | 2 | a0002c0011t0001g0201 a0002c0011t0001g0202 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1059-983G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524379 | |||||||
| chr8:27524479 | C | G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(59): Show |
70 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1059-883C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524479 | |||||||
| chr8:27524683 | C | G | 4 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(1): Show |
7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-679C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524683 | |||||||
| chr8:27524896 | T | C | 1 | a0003c0006t0002g0313 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1059-466T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27524896 | |||||||
| chr8:27524987 | GA | G | 130 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(127): Show |
153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1059-367delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27524987 | ||||||
| chr8:27525068 | C | CTG | 28 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0110 others(25): Show |
37 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1059-255_1059-254d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | ||||||
| chr8:27525068 | C | CTGTG | 18 | a0001c0001t0001g0020 a0001c0001t0001g0153 a0001c0001t0001g0155 others(15): Show |
22 | HG00140.hp1 HG01255.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059-257_1059-254d others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | ||||||
| chr8:27525068 | C | CTGTGTG | 3 | a0001c0001t0001g0139 a0001c0005t0002g0214 a0002c0003t0003g0073 |
3 | HG02004.hp2 HG03195.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1059-259_1059-254d others(8): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | ||||||
| chr8:27525068 | CTG | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
93 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1059-255_1059-254d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | ||||||
| chr8:27525068 | CTGTG | C | 11 | a0001c0001t0001g0042 a0001c0001t0001g0154 a0001c0005t0002g0017 others(8): Show |
12 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1059-257_1059-254d others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | ||||||
| chr8:27525068 | CTGTGTG | C | 4 | a0001c0001t0001g0133 a0001c0005t0003g0095 a0001c0005t0003g0097 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059-259_1059-254d others(8): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | ||||||
| chr8:27525068 | CTGTGTGT others(1): Show |
C | 7 | a0001c0002t0002g0237 a0003c0007t0004g0282 a0003c0007t0004g0283 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059-261_1059-254d others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | ||||||
| chr8:27525068 | CTGTGTGT others(5): Show |
C | 3 | a0001c0002t0002g0203 a0001c0002t0002g0204 a0001c0002t0002g0209 |
3 | HG02896.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1059-265_1059-254d others(14): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | ||||||
| chr8:27525068 | CTGTGTGT others(9): Show |
C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0177 a0011c0027t0001g0170 |
3 | HG00323.hp2 HG01515.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1059-269_1059-254d others(18): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525068 | ||||||
| chr8:27525093 | TGTGTGTG others(19): Show |
T | 2 | a0001c0002t0002g0033 a0001c0002t0002g0236 |
3 | NA19012.hp1 NA19077.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1059-267_1059-242d others(28): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525093 | ||||||
| chr8:27525095 | TGTGTGTG others(7): Show |
T | 8 | a0001c0002t0002g0252 a0001c0004t0003g0011 a0001c0004t0003g0039 others(5): Show |
10 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059-265_1059-252d others(16): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525095 | ||||||
| chr8:27525095 | TGTGTGTG others(11): Show |
T | 1 | a0001c0013t0006g0046 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1059-265_1059-248d others(20): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525095 | ||||||
| chr8:27525095 | TGTGTGTG others(13): Show |
T | 3 | a0001c0002t0002g0004 a0001c0002t0002g0246 a0001c0002t0002g0250 |
6 | NA18949.hp2 NA18956.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059-265_1059-246d others(22): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525095 | ||||||
| chr8:27525097 | T | C | 5 | a0001c0002t0002g0002 a0001c0002t0002g0228 a0001c0002t0002g0229 others(2): Show |
5 | HG01515.hp1 HG01517.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059-265T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525097 | |||||||
| chr8:27525099 | T | C | 10 | a0001c0002t0002g0002 a0001c0002t0002g0228 a0001c0002t0002g0229 others(7): Show |
10 | HG01515.hp1 HG01517.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059-263T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525099 | |||||||
| chr8:27525099 | T | TGC | 23 | a0001c0002t0002g0002 a0001c0002t0002g0029 a0001c0002t0002g0030 others(20): Show |
25 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1059-262_1059-261i others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525099 | ||||||
| chr8:27525099 | T | TGCGC | 4 | a0001c0002t0002g0002 a0001c0002t0002g0222 a0001c0002t0002g0232 others(1): Show |
4 | HG02698.hp1 NA18941.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-262_1059-261i others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525099 | ||||||
| chr8:27525099 | TGTGTGTG others(3): Show |
T | 2 | a0001c0002t0002g0031 a0001c0002t0002g0235 |
2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1059-261_1059-252d others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525099 | ||||||
| chr8:27525101 | T | C | 46 | a0001c0002t0002g0002 a0001c0002t0002g0029 a0001c0002t0002g0030 others(43): Show |
53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1059-261T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525101 | |||||||
| chr8:27525101 | T | TGCGC | 4 | a0001c0002t0002g0032 a0001c0002t0002g0220 a0001c0004t0004g0037 others(1): Show |
4 | HG00621.hp1 HG03130.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-260_1059-259i others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525101 | ||||||
| chr8:27525103 | T | C | 54 | a0001c0002t0002g0002 a0001c0002t0002g0029 a0001c0002t0002g0030 others(51): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1059-259T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525103 | |||||||
| chr8:27525103 | T | TGCGCGC | 4 | a0001c0002t0002g0034 a0001c0002t0002g0251 a0001c0004t0004g0038 others(1): Show |
4 | HG00609.hp2 HG03098.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-258_1059-257i others(8): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525103 | ||||||
| chr8:27525105 | T | A | 1 | a0001c0002t0002g0248 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1059-257T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525105 | |||||||
| chr8:27525105 | T | C | 69 | a0001c0001t0001g0047 a0001c0002t0002g0002 a0001c0002t0002g0012 others(66): Show |
77 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1059-257T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525105 | |||||||
| chr8:27525105 | T | TGCGCGCG others(3): Show |
1 | a0001c0002t0002g0218 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1059-256_1059-255i others(12): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525105 | ||||||
| chr8:27525107 | T | C | 96 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0047 others(93): Show |
109 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1059-255T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525107 | |||||||
| chr8:27525107 | T | TGC | 10 | a0001c0001t0001g0041 a0001c0001t0001g0118 a0001c0001t0001g0158 others(7): Show |
10 | HG02602.hp1 HG03139.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059-240_1059-239d others(4): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | ||||||
| chr8:27525107 | T | TGCGC | 3 | a0001c0001t0001g0123 a0001c0004t0004g0291 a0002c0003t0003g0066 |
3 | HG00544.hp1 HG02486.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1059-242_1059-239d others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | ||||||
| chr8:27525107 | T | TGTGC | 7 | a0001c0004t0004g0290 a0001c0004t0004g0292 a0001c0014t0003g0298 others(4): Show |
7 | HG01243.hp2 HG02258.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059-254_1059-253i others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | ||||||
| chr8:27525107 | T | TGTGCGCG others(5): Show |
2 | a0001c0004t0004g0037 a0001c0004t0004g0038 |
2 | HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1059-254_1059-253i others(14): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | ||||||
| chr8:27525107 | T | TGTGCGCG others(11): Show |
1 | a0001c0013t0002g0045 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1059-254_1059-253i others(20): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | ||||||
| chr8:27525107 | T | TGTGTGCG others(9): Show |
1 | a0001c0002t0002g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1059-254_1059-253i others(18): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | ||||||
| chr8:27525107 | T | TGTGTGTG others(1): Show |
3 | a0001c0014t0003g0297 a0002c0003t0003g0065 a0002c0003t0003g0208 |
3 | HG01192.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1059-254_1059-253i others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | 27525107 | ||||||
| chr8:27525109 | C | T | 5 | a0001c0001t0001g0270 a0001c0013t0002g0233 a0003c0007t0004g0278 others(2): Show |
5 | HG00733.hp1 HG00738.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059-253C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525109 | |||||||
| chr8:27525111 | C | T | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG00558.hp1 HG02027.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-251C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525111 | |||||||
| chr8:27525114 | G | A | 1 | a0001c0014t0003g0297 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1059-248G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525114 | |||||||
| chr8:27525116 | G | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1059-246G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 11/18 | chr8 | 27525116 | |||||||
| chr8:27525498 | A | G | 1 | a0001c0005t0006g0102 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1170+25A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525498 | |||||||
| chr8:27525706 | T | A | 9 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(6): Show |
10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+233T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525706 | |||||||
| chr8:27525712 | G | GA | 9 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(6): Show |
10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+240dupA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27525712 | ||||||
| chr8:27525845 | A | G | 1 | a0003c0006t0002g0305 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1170+372A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525845 | |||||||
| chr8:27525913 | G | T | 2 | a0002c0011t0001g0201 a0002c0011t0001g0202 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1170+440G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525913 | |||||||
| chr8:27525999 | C | T | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1170+526C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27525999 | |||||||
| chr8:27526019 | C | T | 1 | a0004c0010t0001g0262 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1170+546C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526019 | |||||||
| chr8:27526187 | C | T | 7 | a0003c0006t0002g0309 a0003c0007t0004g0278 a0003c0007t0004g0279 others(4): Show |
7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+714C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526187 | |||||||
| chr8:27526250 | C | T | 7 | a0003c0006t0002g0309 a0003c0007t0004g0278 a0003c0007t0004g0279 others(4): Show |
7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+777C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526250 | |||||||
| chr8:27526384 | G | T | 59 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(56): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1170+911G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526384 | |||||||
| chr8:27526896 | G | T | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1170+1423G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526896 | |||||||
| chr8:27526989 | G | A | 33 | a0001c0001t0001g0040 a0001c0004t0003g0011 a0001c0004t0003g0039 others(30): Show |
36 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1170+1516G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27526989 | |||||||
| chr8:27527002 | G | T | 1 | a0001c0002t0002g0242 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1170+1529G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527002 | |||||||
| chr8:27527315 | C | T | 6 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0220 others(3): Show |
8 | HG02723.hp1 HG02970.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170+1842C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527315 | |||||||
| chr8:27527359 | T | C | 10 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+1886T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527359 | |||||||
| chr8:27527414 | T | C | 7 | a0003c0006t0002g0309 a0003c0007t0004g0278 a0003c0007t0004g0279 others(4): Show |
7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+1941T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527414 | |||||||
| chr8:27527760 | G | A | 1 | a0003c0007t0004g0282 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1170+2287G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527760 | |||||||
| chr8:27527898 | C | T | 128 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(125): Show |
151 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1170+2425C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527898 | |||||||
| chr8:27527933 | A | G | 95 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(92): Show |
115 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1170+2460A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527933 | |||||||
| chr8:27527948 | G | A | 7 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(4): Show |
10 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+2475G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27527948 | |||||||
| chr8:27528035 | G | A | 2 | a0003c0006t0002g0303 a0003c0006t0002g0304 |
2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1170+2562G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528035 | |||||||
| chr8:27528185 | T | C | 1 | a0003c0006t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1170+2712T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528185 | |||||||
| chr8:27528349 | T | A | 17 | a0001c0001t0001g0040 a0003c0007t0004g0280 a0003c0007t0004g0281 others(14): Show |
18 | HG00639.hp2 HG01192.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1170+2876T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528349 | |||||||
| chr8:27528400 | G | T | 7 | a0003c0006t0002g0309 a0003c0007t0004g0278 a0003c0007t0004g0279 others(4): Show |
7 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+2927G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528400 | |||||||
| chr8:27528449 | C | T | 1 | a0001c0002t0002g0242 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1170+2976C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528449 | |||||||
| chr8:27528516 | T | C | 1 | a0002c0003t0003g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1170+3043T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528516 | |||||||
| chr8:27528522 | T | G | 2 | a0002c0008t0002g0058 a0002c0008t0002g0078 |
2 | NA18955.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1170+3049T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528522 | |||||||
| chr8:27528523 | G | T | 9 | a0001c0001t0001g0040 a0004c0010t0001g0257 a0004c0010t0001g0258 others(6): Show |
10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+3050G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528523 | |||||||
| chr8:27528592 | A | G | 2 | a0002c0003t0003g0053 a0002c0003t0003g0054 |
2 | NA19062.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1170+3119A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528592 | |||||||
| chr8:27528736 | T | A | 1 | a0005c0009t0001g0186 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1170+3263T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528736 | |||||||
| chr8:27528878 | C | T | 2 | a0003c0006t0002g0276 a0003c0006t0002g0277 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1170+3405C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528878 | |||||||
| chr8:27528920 | C | T | 3 | a0003c0007t0004g0280 a0003c0007t0004g0281 a0003c0007t0004g0287 |
3 | HG02615.hp1 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1170+3447C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528920 | |||||||
| chr8:27528921 | G | A | 10 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+3448G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27528921 | |||||||
| chr8:27529078 | G | A | 9 | a0001c0001t0001g0040 a0004c0010t0001g0257 a0004c0010t0001g0258 others(6): Show |
10 | HG00639.hp2 HG01192.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+3605G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529078 | |||||||
| chr8:27529115 | C | T | 1 | a0002c0003t0003g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1170+3642C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529115 | |||||||
| chr8:27529253 | T | C | 2 | a0010c0033t0004g0043 a0013c0037t0004g0044 |
2 | HG00738.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1170+3780T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529253 | |||||||
| chr8:27529408 | ACTTGGCC others(6): Show |
A | 1 | a0017c0022t0002g0238 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1170+3936_1170+394 others(17): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529408 | |||||||
| chr8:27529457 | G | T | 24 | a0001c0001t0001g0040 a0001c0004t0003g0011 a0001c0004t0003g0039 others(21): Show |
27 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1170+3984G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529457 | |||||||
| chr8:27529498 | C | T | 10 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+4025C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529498 | |||||||
| chr8:27529499 | G | A | 1 | a0003c0007t0004g0286 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1170+4026G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529499 | |||||||
| chr8:27529653 | G | A | 1 | a0001c0002t0002g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1170+4180G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529653 | |||||||
| chr8:27529713 | C | G | 130 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(127): Show |
153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1170+4240C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529713 | |||||||
| chr8:27529791 | A | G | 61 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(58): Show |
75 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1170+4318A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529791 | |||||||
| chr8:27529875 | C | T | 98 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(95): Show |
118 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1170+4402C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529875 | |||||||
| chr8:27529885 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0136 |
2 | NA18972.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1170+4412T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529885 | |||||||
| chr8:27529888 | GC | G | 4 | a0007c0012t0001g0266 a0007c0012t0001g0268 a0009c0018t0001g0267 others(1): Show |
4 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170+4416delC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27529888 | |||||||
| chr8:27529889 | CA | C | 130 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(127): Show |
153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1170+4430delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27529889 | ||||||
| chr8:27530067 | CT | C | 130 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(127): Show |
153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1170+4607delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27530067 | ||||||
| chr8:27530075 | T | C | 1 | a0003c0006t0002g0309 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1170+4602T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530075 | |||||||
| chr8:27530117 | G | A | 7 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(4): Show |
9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+4644G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530117 | |||||||
| chr8:27530192 | G | A | 1 | a0001c0002t0002g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1170+4719G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530192 | |||||||
| chr8:27530227 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0001g0138 others(1): Show |
4 | HG01891.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4754C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530227 | |||||||
| chr8:27530250 | G | A | 6 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0004c0015t0004g0254 others(3): Show |
6 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+4777G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530250 | |||||||
| chr8:27530269 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1170+4796A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530269 | |||||||
| chr8:27530328 | A | C | 20 | a0001c0005t0003g0071 a0002c0003t0002g0070 a0002c0003t0002g0083 others(17): Show |
28 | HG00140.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1170+4855A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530328 | |||||||
| chr8:27530331 | G | T | 6 | a0003c0007t0004g0278 a0003c0007t0004g0279 a0004c0015t0004g0254 others(3): Show |
6 | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+4858G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530331 | |||||||
| chr8:27530355 | G | A | 20 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(17): Show |
21 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1170+4882G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530355 | |||||||
| chr8:27530446 | A | G | 1 | a0002c0003t0003g0069 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1170+4973A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530446 | |||||||
| chr8:27530642 | C | A | 2 | a0001c0014t0003g0298 a0001c0014t0003g0299 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1170+5169C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530642 | |||||||
| chr8:27530659 | T | TATTTTGA others(15): Show |
1 | a0001c0002t0002g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1170+5187_1170+520 others(26): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27530659 | ||||||
| chr8:27530682 | G | A | 106 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(103): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1170+5209G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530682 | |||||||
| chr8:27530762 | CT | C | 94 | a0001c0001t0001g0211 a0001c0001t0001g0245 a0001c0002t0002g0002 others(91): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1170+5307delT | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27530762 | ||||||
| chr8:27530762 | CTT | C | 16 | a0001c0001t0001g0040 a0001c0002t0002g0216 a0001c0002t0002g0217 others(13): Show |
17 | HG00639.hp2 HG01192.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1170+5306_1170+530 others(6): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27530762 | ||||||
| chr8:27530803 | C | G | 130 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(127): Show |
153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1170+5330C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530803 | |||||||
| chr8:27530828 | A | T | 106 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(103): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1170+5355A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530828 | |||||||
| chr8:27530891 | G | A | 10 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1170+5418G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530891 | |||||||
| chr8:27530965 | G | A | 1 | a0005c0009t0001g0186 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1170+5492G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27530965 | |||||||
| chr8:27531015 | G | A | 9 | a0002c0008t0002g0061 a0003c0007t0004g0280 a0003c0007t0004g0281 others(6): Show |
9 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+5542G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531015 | |||||||
| chr8:27531059 | G | T | 2 | a0003c0006t0002g0276 a0003c0006t0002g0277 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1170+5586G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531059 | |||||||
| chr8:27531276 | C | T | 1 | a0002c0008t0002g0062 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1171-5508C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531276 | |||||||
| chr8:27531435 | G | A | 9 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(6): Show |
10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1171-5349G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531435 | |||||||
| chr8:27531538 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1171-5246A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531538 | |||||||
| chr8:27531570 | C | T | 1 | a0003c0006t0002g0309 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1171-5214C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531570 | |||||||
| chr8:27531575 | C | T | 1 | a0001c0002t0002g0231 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1171-5209C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531575 | |||||||
| chr8:27531604 | T | C | 10 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(7): Show |
12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-5180T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531604 | |||||||
| chr8:27531650 | G | A | 28 | a0001c0001t0001g0040 a0001c0004t0003g0011 a0001c0004t0003g0039 others(25): Show |
33 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1171-5134G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531650 | |||||||
| chr8:27531688 | G | A | 2 | a0001c0002t0002g0228 a0001c0002t0002g0229 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1171-5096G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531688 | |||||||
| chr8:27531710 | A | G | 1 | a0001c0005t0003g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1171-5074A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531710 | |||||||
| chr8:27531743 | T | C | 2 | a0010c0033t0004g0043 a0013c0037t0004g0044 |
2 | HG00738.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1171-5041T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531743 | |||||||
| chr8:27531782 | C | T | 10 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(7): Show |
13 | HG01243.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1171-5002C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531782 | |||||||
| chr8:27531917 | C | G | 2 | a0003c0007t0004g0283 a0003c0007t0004g0285 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1171-4867C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531917 | |||||||
| chr8:27531918 | A | G | 1 | a0001c0005t0003g0071 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1171-4866A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531918 | |||||||
| chr8:27531939 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0130 others(3): Show |
9 | HG00642.hp2 HG00741.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1171-4845C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531939 | |||||||
| chr8:27531940 | G | A | 128 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(125): Show |
151 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1171-4844G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531940 | |||||||
| chr8:27531941 | C | A | 1 | a0001c0002t0002g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1171-4843C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27531941 | |||||||
| chr8:27532006 | G | A | 60 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(57): Show |
74 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1171-4778G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532006 | |||||||
| chr8:27532021 | A | G | 1 | a0001c0002t0002g0240 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1171-4763A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532021 | |||||||
| chr8:27532025 | T | C | 131 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(128): Show |
154 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.1171-4759T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532025 | |||||||
| chr8:27532101 | A | T | 7 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(4): Show |
9 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1171-4683A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532101 | |||||||
| chr8:27532114 | G | A | 12 | a0001c0001t0001g0091 a0001c0001t0001g0113 a0001c0001t0001g0148 others(9): Show |
13 | HG00323.hp1 HG00733.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1171-4670G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532114 | |||||||
| chr8:27532185 | C | T | 12 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(9): Show |
12 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1171-4599C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532185 | |||||||
| chr8:27532258 | G | A | 1 | a0001c0014t0003g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1171-4526G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532258 | |||||||
| chr8:27532511 | G | A | 10 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1171-4273G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532511 | |||||||
| chr8:27532552 | T | C | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1171-4232T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532552 | |||||||
| chr8:27532615 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1171-4169G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532615 | |||||||
| chr8:27532675 | G | A | 134 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(131): Show |
157 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1171-4109G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532675 | |||||||
| chr8:27532729 | T | G | 59 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(56): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1171-4055T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532729 | |||||||
| chr8:27532799 | C | T | 1 | a0001c0005t0002g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1171-3985C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532799 | |||||||
| chr8:27532858 | A | G | 9 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(6): Show |
10 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1171-3926A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532858 | |||||||
| chr8:27532977 | T | G | 3 | a0003c0006t0002g0302 a0003c0006t0002g0312 a0003c0006t0002g0313 |
3 | HG02293.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1171-3807T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27532977 | |||||||
| chr8:27533080 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1171-3704A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533080 | |||||||
| chr8:27533101 | C | A | 2 | a0002c0003t0003g0068 a0002c0003t0003g0069 |
2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1171-3683C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533101 | |||||||
| chr8:27533203 | A | G | 1 | a0003c0007t0008g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1171-3581A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533203 | |||||||
| chr8:27533293 | C | G | 1 | a0001c0001t0001g0041 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1171-3491C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533293 | |||||||
| chr8:27533423 | A | G | 1 | a0015c0036t0002g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1171-3361A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533423 | |||||||
| chr8:27533438 | G | A | 7 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(4): Show |
10 | HG02257.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1171-3346G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533438 | |||||||
| chr8:27533603 | TA | T | 6 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0196 others(3): Show |
6 | HG00423.hp1 NA18951.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-3179delA | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27533603 | ||||||
| chr8:27533674 | A | C | 102 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(99): Show |
120 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1171-3110A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533674 | |||||||
| chr8:27533842 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1171-2942C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533842 | |||||||
| chr8:27533843 | C | A | 11 | a0001c0001t0001g0040 a0002c0011t0001g0201 a0002c0011t0001g0202 others(8): Show |
12 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1171-2941C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533843 | |||||||
| chr8:27533848 | G | A | 59 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(56): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1171-2936G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533848 | |||||||
| chr8:27533919 | C | T | 10 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(7): Show |
12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-2865C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27533919 | |||||||
| chr8:27534063 | G | A | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1171-2721G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534063 | |||||||
| chr8:27534103 | G | C | 133 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(130): Show |
156 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1171-2681G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534103 | |||||||
| chr8:27534139 | T | C | 2 | a0003c0006t0002g0276 a0003c0006t0002g0277 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1171-2645T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534139 | |||||||
| chr8:27534143 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1171-2641G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534143 | |||||||
| chr8:27534272 | C | T | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-2512C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534272 | |||||||
| chr8:27534286 | T | C | 3 | a0002c0003t0003g0052 a0002c0003t0003g0053 a0002c0003t0003g0054 |
3 | NA18952.hp1 NA19062.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1171-2498T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534286 | |||||||
| chr8:27534288 | T | A | 5 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 others(2): Show |
5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1171-2496T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534288 | |||||||
| chr8:27534323 | G | A | 2 | a0002c0008t0002g0058 a0002c0008t0002g0078 |
2 | NA18955.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1171-2461G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534323 | |||||||
| chr8:27534407 | T | C | 10 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(7): Show |
12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-2377T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534407 | |||||||
| chr8:27534408 | T | C | 8 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(5): Show |
9 | HG01884.hp2 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1171-2376T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534408 | |||||||
| chr8:27534424 | G | A | 1 | a0003c0007t0004g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1171-2360G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534424 | |||||||
| chr8:27534601 | G | A | 1 | a0003c0007t0004g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1171-2183G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534601 | |||||||
| chr8:27534645 | AAAAAAT | A | 11 | a0001c0001t0001g0040 a0002c0011t0001g0201 a0002c0011t0001g0202 others(8): Show |
12 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1171-2127_1171-212 others(10): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27534645 | ||||||
| chr8:27534705 | G | A | 1 | a0002c0003t0003g0075 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1171-2079G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534705 | |||||||
| chr8:27534740 | T | A | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-2044T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534740 | |||||||
| chr8:27534873 | C | T | 1 | a0002c0008t0002g0057 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1171-1911C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534873 | |||||||
| chr8:27534878 | T | C | 59 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(56): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1171-1906T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534878 | |||||||
| chr8:27534922 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG00558.hp1 HG02080.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1171-1862C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27534922 | |||||||
| chr8:27535026 | C | G | 10 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(7): Show |
12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-1758C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535026 | |||||||
| chr8:27535158 | C | T | 2 | a0003c0007t0004g0278 a0003c0007t0004g0279 |
2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1171-1626C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535158 | |||||||
| chr8:27535163 | A | ATATTT | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-1600_1171-159 others(9): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27535163 | ||||||
| chr8:27535163 | ATATTTTA others(8): Show |
A | 10 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1171-1610_1171-159 others(19): Show |
EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | 27535163 | ||||||
| chr8:27535427 | G | A | 3 | a0003c0006t0002g0302 a0003c0006t0002g0312 a0003c0006t0002g0313 |
3 | HG02293.hp1 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1171-1357G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535427 | |||||||
| chr8:27535469 | C | T | 107 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(104): Show |
126 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1171-1315C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535469 | |||||||
| chr8:27535470 | G | T | 1 | a0001c0002t0002g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1171-1314G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535470 | |||||||
| chr8:27535536 | T | C | 10 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1171-1248T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535536 | |||||||
| chr8:27535549 | G | A | 102 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(99): Show |
120 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1171-1235G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535549 | |||||||
| chr8:27535593 | C | T | 1 | a0001c0002t0002g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1171-1191C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535593 | |||||||
| chr8:27535634 | C | A | 1 | a0003c0035t0001g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1171-1150C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535634 | |||||||
| chr8:27535703 | T | G | 131 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(128): Show |
153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1171-1081T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535703 | |||||||
| chr8:27535939 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1171-845T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27535939 | |||||||
| chr8:27536015 | C | T | 4 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(1): Show |
7 | HG02257.hp1 HG02970.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1171-769C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536015 | |||||||
| chr8:27536063 | G | C | 1 | a0002c0003t0003g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1171-721G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536063 | |||||||
| chr8:27536186 | A | C | 1 | a0001c0001t0001g0027 | 2 | NA18939.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1171-598A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536186 | |||||||
| chr8:27536205 | G | A | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1171-579G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536205 | |||||||
| chr8:27536347 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1171-437G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536347 | |||||||
| chr8:27536436 | C | T | 10 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(7): Show |
12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-348C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536436 | |||||||
| chr8:27536501 | A | G | 11 | a0001c0001t0001g0040 a0002c0011t0001g0201 a0002c0011t0001g0202 others(8): Show |
12 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1171-283A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536501 | |||||||
| chr8:27536542 | A | G | 1 | a0002c0003t0003g0076 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1171-242A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536542 | |||||||
| chr8:27536547 | G | C | 2 | a0003c0007t0008g0272 a0003c0007t0008g0273 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1171-237G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536547 | |||||||
| chr8:27536575 | G | A | 1 | a0003c0006t0002g0309 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1171-209G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536575 | |||||||
| chr8:27536582 | A | G | 10 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(7): Show |
12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1171-202A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536582 | |||||||
| chr8:27536740 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0130 others(3): Show |
9 | HG00642.hp2 HG00741.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1171-44C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 12/18 | chr8 | 27536740 | |||||||
| chr8:27536870 | T | C | 29 | a0001c0001t0001g0040 a0001c0004t0003g0011 a0001c0004t0003g0039 others(26): Show |
33 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1242+15T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27536870 | |||||||
| chr8:27536917 | C | A | 1 | a0019c0026t0002g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1242+62C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27536917 | |||||||
| chr8:27536999 | C | G | 5 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 others(2): Show |
5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+144C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27536999 | |||||||
| chr8:27537022 | G | A | 13 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(10): Show |
13 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1242+167G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537022 | |||||||
| chr8:27537207 | G | C | 133 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(130): Show |
155 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1242+352G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537207 | |||||||
| chr8:27537210 | G | A | 11 | a0001c0001t0001g0040 a0002c0011t0001g0201 a0002c0011t0001g0202 others(8): Show |
12 | HG00639.hp2 HG01192.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.1242+355G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537210 | |||||||
| chr8:27537354 | C | T | 5 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 others(2): Show |
5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+499C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537354 | |||||||
| chr8:27537440 | C | A | 104 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(101): Show |
122 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1242+585C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537440 | |||||||
| chr8:27537465 | G | A | 1 | a0001c0002t0002g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1242+610G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537465 | |||||||
| chr8:27537485 | T | C | 5 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 others(2): Show |
5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+630T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537485 | |||||||
| chr8:27537581 | A | G | 2 | a0002c0003t0003g0048 a0002c0003t0003g0049 |
2 | HG00140.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1242+726A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537581 | |||||||
| chr8:27537691 | T | A | 1 | a0001c0002t0002g0232 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1242+836T>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537691 | |||||||
| chr8:27537732 | T | C | 104 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(101): Show |
122 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1242+877T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537732 | |||||||
| chr8:27537751 | A | G | 5 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 others(2): Show |
5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242+896A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537751 | |||||||
| chr8:27537937 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1243-722A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537937 | |||||||
| chr8:27537943 | C | T | 8 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(5): Show |
9 | HG02486.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1243-716C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537943 | |||||||
| chr8:27537999 | G | A | 2 | a0004c0015t0004g0254 a0004c0015t0004g0255 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1243-660G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27537999 | |||||||
| chr8:27538147 | G | T | 10 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(7): Show |
13 | HG01243.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1243-512G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538147 | |||||||
| chr8:27538394 | C | T | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1243-265C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538394 | |||||||
| chr8:27538472 | C | T | 2 | a0001c0002t0002g0223 a0001c0002t0002g0227 |
2 | HG00438.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1243-187C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538472 | |||||||
| chr8:27538594 | G | T | 104 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(101): Show |
122 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1243-65G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538594 | |||||||
| chr8:27538599 | G | A | 8 | a0003c0007t0004g0280 a0003c0007t0004g0281 a0003c0007t0004g0282 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243-60G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 13/18 | chr8 | 27538599 | |||||||
| chr8:27538746 | A | G | 1 | a0011c0027t0001g0170 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1276+54A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538746 | |||||||
| chr8:27538827 | C | T | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276+135C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538827 | |||||||
| chr8:27538852 | C | G | 3 | a0003c0007t0004g0280 a0003c0007t0004g0281 a0003c0007t0004g0287 |
3 | HG02615.hp1 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1276+160C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538852 | |||||||
| chr8:27538858 | C | G | 1 | a0003c0006t0002g0309 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1276+166C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538858 | |||||||
| chr8:27538935 | G | C | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276+243G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27538935 | |||||||
| chr8:27539006 | T | C | 133 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(130): Show |
155 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1276+314T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539006 | |||||||
| chr8:27539030 | T | C | 29 | a0001c0001t0001g0040 a0001c0004t0003g0011 a0001c0004t0003g0039 others(26): Show |
33 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1276+338T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539030 | |||||||
| chr8:27539096 | C | T | 10 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0295 others(7): Show |
12 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1276+404C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539096 | |||||||
| chr8:27539350 | C | T | 3 | a0001c0014t0003g0297 a0001c0014t0003g0298 a0001c0014t0003g0299 |
3 | HG01243.hp2 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1276+658C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539350 | |||||||
| chr8:27539384 | C | G | 2 | a0004c0010t0007g0260 a0004c0010t0007g0261 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1276+692C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539384 | |||||||
| chr8:27539511 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1276+819C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539511 | |||||||
| chr8:27539570 | C | T | 33 | a0001c0005t0003g0137 a0001c0005t0003g0171 a0002c0003t0003g0001 others(30): Show |
45 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1276+878C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539570 | |||||||
| chr8:27539640 | T | C | 133 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(130): Show |
155 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1277-914T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539640 | |||||||
| chr8:27539652 | C | G | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-902C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539652 | |||||||
| chr8:27539709 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1277-845C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539709 | |||||||
| chr8:27539734 | C | T | 7 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(4): Show |
8 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1277-820C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539734 | |||||||
| chr8:27539846 | C | T | 11 | a0003c0006t0002g0276 a0003c0006t0002g0277 a0003c0006t0002g0302 others(8): Show |
11 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1277-708C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539846 | |||||||
| chr8:27539852 | C | G | 16 | a0001c0002t0002g0216 a0001c0002t0002g0217 a0001c0002t0002g0218 others(13): Show |
17 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1277-702C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539852 | |||||||
| chr8:27539881 | G | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG02083.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1277-673G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539881 | |||||||
| chr8:27539902 | C | T | 3 | a0003c0007t0008g0272 a0003c0007t0008g0273 a0003c0007t0012g0284 |
3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1277-652C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539902 | |||||||
| chr8:27539976 | G | T | 3 | a0003c0007t0008g0272 a0003c0007t0008g0273 a0003c0007t0012g0284 |
3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1277-578G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539976 | |||||||
| chr8:27539982 | A | G | 1 | a0002c0003t0003g0080 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1277-572A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27539982 | |||||||
| chr8:27540069 | G | T | 2 | a0004c0015t0004g0254 a0004c0015t0004g0255 |
2 | HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1277-485G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540069 | |||||||
| chr8:27540153 | C | T | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-401C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540153 | |||||||
| chr8:27540166 | C | T | 10 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(7): Show |
10 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1277-388C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540166 | |||||||
| chr8:27540213 | C | T | 2 | a0003c0007t0004g0278 a0003c0007t0004g0279 |
2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1277-341C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540213 | |||||||
| chr8:27540317 | C | T | 13 | a0001c0004t0004g0037 a0001c0004t0004g0038 a0001c0004t0004g0290 others(10): Show |
15 | HG00733.hp1 HG00738.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1277-237C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540317 | |||||||
| chr8:27540364 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | NA18989.hp1 NA19000.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1277-190C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540364 | |||||||
| chr8:27540369 | G | A | 7 | a0003c0007t0004g0280 a0003c0007t0004g0281 a0003c0007t0004g0282 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-185G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540369 | |||||||
| chr8:27540373 | A | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0050 others(9): Show |
14 | HG01891.hp1 HG02451.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1277-181A>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540373 | |||||||
| chr8:27540454 | C | T | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-100C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540454 | |||||||
| chr8:27540552 | A | G | 1 | a0001c0004t0004g0292 | 1 | NA19240.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1277-2A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 14/18 | chr8 | 27540552 | |||||||
| chr8:27540915 | T | C | 176 | a0001c0001t0001g0040 a0001c0001t0001g0122 a0001c0002t0002g0002 others(173): Show |
210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1379+259T>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/18 | chr8 | 27540915 | |||||||
| chr8:27541103 | C | T | 47 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(44): Show |
62 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1380-370C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/18 | chr8 | 27541103 | |||||||
| chr8:27541159 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1380-314C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/18 | chr8 | 27541159 | |||||||
| chr8:27541296 | G | A | 32 | a0001c0001t0001g0040 a0001c0004t0003g0011 a0001c0004t0003g0039 others(29): Show |
36 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1380-177G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 15/18 | chr8 | 27541296 | |||||||
| chr8:27541594 | G | A | 7 | a0003c0007t0004g0280 a0003c0007t0004g0281 a0003c0007t0004g0282 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1449+52G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27541594 | |||||||
| chr8:27541656 | G | A | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1449+114G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27541656 | |||||||
| chr8:27541909 | A | G | 1 | a0001c0002t0002g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1449+367A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27541909 | |||||||
| chr8:27541957 | C | A | 2 | a0003c0007t0004g0278 a0003c0007t0004g0279 |
2 | HG00733.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1449+415C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27541957 | |||||||
| chr8:27542001 | G | C | 41 | a0001c0005t0003g0071 a0001c0005t0003g0137 a0001c0005t0003g0171 others(38): Show |
53 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.1449+459G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542001 | |||||||
| chr8:27542187 | A | G | 175 | a0001c0001t0001g0040 a0001c0002t0002g0002 a0001c0002t0002g0004 others(172): Show |
209 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1449+645A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542187 | |||||||
| chr8:27542314 | A | C | 5 | a0001c0013t0002g0045 a0001c0013t0002g0233 a0001c0013t0006g0046 others(2): Show |
5 | HG02027.hp2 NA18950.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1449+772A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542314 | |||||||
| chr8:27542494 | A | G | 1 | a0003c0006t0002g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1449+952A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542494 | |||||||
| chr8:27542527 | G | A | 49 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(46): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1449+985G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542527 | |||||||
| chr8:27542527 | G | C | 5 | a0007c0012t0001g0265 a0007c0012t0001g0266 a0007c0012t0001g0268 others(2): Show |
5 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+985G>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542527 | |||||||
| chr8:27542551 | G | A | 22 | a0001c0001t0001g0040 a0001c0001t0001g0091 a0001c0001t0001g0113 others(19): Show |
24 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.1449+1009G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542551 | |||||||
| chr8:27542574 | G | A | 3 | a0003c0007t0008g0272 a0003c0007t0008g0273 a0003c0007t0012g0284 |
3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1449+1032G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542574 | |||||||
| chr8:27542711 | G | T | 2 | a0003c0006t0002g0276 a0003c0006t0002g0277 |
2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1450-1038G>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542711 | |||||||
| chr8:27542849 | G | A | 3 | a0003c0007t0008g0272 a0003c0007t0008g0273 a0003c0007t0012g0284 |
3 | HG02723.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1450-900G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27542849 | |||||||
| chr8:27543006 | T | TC | 32 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0091 others(29): Show |
33 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1450-734dupC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 27543006 | ||||||
| chr8:27543006 | TC | T | 143 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(140): Show |
175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1450-734delC | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr8 | 27543006 | ||||||
| chr8:27543012 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1450-737C>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543012 | |||||||
| chr8:27543013 | C | A | 7 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(4): Show |
8 | HG01516.hp1 HG01517.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1450-736C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543013 | |||||||
| chr8:27543015 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1450-734C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543015 | |||||||
| chr8:27543023 | G | A | 59 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0012 others(56): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1450-726G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543023 | |||||||
| chr8:27543075 | A | C | 70 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(67): Show |
85 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1450-674A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543075 | |||||||
| chr8:27543087 | C | T | 70 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(67): Show |
85 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1450-662C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543087 | |||||||
| chr8:27543142 | G | A | 1 | a0006c0020t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1450-607G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543142 | |||||||
| chr8:27543165 | A | G | 45 | a0001c0005t0003g0071 a0001c0005t0003g0095 a0001c0005t0003g0096 others(42): Show |
57 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1450-584A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543165 | |||||||
| chr8:27543324 | A | C | 1 | a0001c0001t0006g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1450-425A>C | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543324 | |||||||
| chr8:27543386 | T | G | 11 | a0003c0006t0002g0302 a0003c0006t0002g0303 a0003c0006t0002g0304 others(8): Show |
11 | HG00642.hp1 HG00733.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1450-363T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543386 | |||||||
| chr8:27543441 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1450-308G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543441 | |||||||
| chr8:27543490 | A | G | 1 | a0002c0003t0003g0084 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1450-259A>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543490 | |||||||
| chr8:27543506 | T | G | 1 | a0018c0028t0001g0178 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1450-243T>G | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543506 | |||||||
| chr8:27543616 | G | A | 3 | a0003c0007t0004g0280 a0003c0007t0004g0281 a0003c0007t0004g0287 |
3 | HG02615.hp1 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1450-133G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543616 | |||||||
| chr8:27543625 | G | A | 51 | a0001c0004t0003g0010 a0001c0004t0003g0035 a0001c0004t0003g0288 others(48): Show |
66 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1450-124G>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 16/18 | chr8 | 27543625 | |||||||
| chr8:27543849 | C | T | 2 | a0001c0013t0002g0045 a0001c0013t0006g0046 |
2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1530+20C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27543849 | |||||||
| chr8:27543864 | C | T | 2 | a0001c0005t0003g0137 a0002c0003t0003g0080 |
2 | HG00408.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1530+35C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27543864 | |||||||
| chr8:27543900 | C | T | 2 | a0001c0002t0002g0237 a0001c0002t0002g0239 |
2 | HG02129.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1530+71C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27543900 | |||||||
| chr8:27544087 | C | A | 6 | a0001c0005t0002g0017 a0001c0005t0002g0092 a0001c0005t0002g0093 others(3): Show |
7 | HG02486.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1531-99C>A | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27544087 | |||||||
| chr8:27544105 | C | T | 6 | a0001c0004t0003g0011 a0001c0004t0003g0039 a0001c0004t0003g0293 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-81C>T | EPHX2 | ENSG00000120915.14 | transcript | ENST00000521400.6 | protein_coding | 17/18 | chr8 | 27544105 |