Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 387712 |
| ensemblid | ENSG00000188316.16 |
| hgncid | 31670 |
| symbol | ENO4 |
| name | enolase 4 |
| refseq_nuc | NM_001242699.2 |
| refseq_prot | NP_001229628.1 |
| ensembl_nuc | ENST00000341276.11 |
| ensembl_prot | ENSP00000345555.6 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 116849499 |
| end | 116882601 |
| strand | + |
| ver | v1.2 |
| region | chr10:116849499-116882601 |
| region5000 | chr10:116844499-116887601 |
| regionname0 | ENO4_chr10_116849499_116882601 |
| regionname5000 | ENO4_chr10_116844499_116887601 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 625 | 382 | 82 | 72 | 176 | 14 | 38 | 134 | ENO4_chr10_116844499_116887601 | ENO4 | MEEEG others(620): Show |
chr10 | 116844499 | 116887601 |
| a0002 | 0/0 | 625 | 9 | 0 | 0 | 9 | 0 | 0 | 6 | ENO4_chr10_116844499_116887601 | ENO4 | MEEEG others(620): Show |
chr10 | 116844499 | 116887601 |
| a0003 | 0/0 | 625 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | MEEEG others(620): Show |
chr10 | 116844499 | 116887601 |
| a0004 | 0/0 | 625 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | MEEEG others(620): Show |
chr10 | 116844499 | 116887601 |
| a0005 | 0/0 | 363 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | MEEEG others(358): Show |
chr10 | 116844499 | 116887601 |
| a0006 | 0/0 | 625 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | MEEEG others(620): Show |
chr10 | 116844499 | 116887601 |
| a0007 | 0/0 | 625 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | MEEEG others(620): Show |
chr10 | 116844499 | 116887601 |
| a0008 | 0/0 | 410 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | MEEEG others(405): Show |
chr10 | 116844499 | 116887601 |
| a0009 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | MEEEG others(356): Show |
chr10 | 116844499 | 116887601 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1875 | 162 | 46 | 15 | 83 | 4 | 14 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0001c0002 | 0/0 | 1875 | 151 | 30 | 30 | 74 | 2 | 15 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0001c0003 | 0/0 | 1875 | 65 | 6 | 26 | 17 | 8 | 8 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0001c0006 | 0/0 | 1875 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0001c0009 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0001c0011 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0001c0014 | 0/0 | 1875 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0002c0004 | 0/0 | 1875 | 9 | 0 | 0 | 9 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0003c0013 | 0/0 | 1875 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0004c0015 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0005c0010 | 0/0 | 1873 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1868): Show |
chr10 | 116844499 | 116887601 | ||
| a0006c0008 | 0/0 | 1875 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0007c0005 | 0/0 | 1875 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1870): Show |
chr10 | 116844499 | 116887601 | ||
| a0008c0012 | 0/0 | 1877 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1872): Show |
chr10 | 116844499 | 116887601 | ||
| a0009c0007 | 0/0 | 1873 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | ATGGA others(1868): Show |
chr10 | 116844499 | 116887601 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2878 | 84 | 18 | 12 | 38 | 2 | 14 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0002 | 0/0 | 2879 | 32 | 8 | 1 | 23 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0003 | 0/0 | 2880 | 4 | 0 | 0 | 4 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0004 | 0/0 | 2880 | 3 | 1 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0005 | 0/0 | 2877 | 23 | 8 | 0 | 15 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2872): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0008 | 0/0 | 2879 | 2 | 0 | 0 | 0 | 2 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0009 | 0/0 | 2873 | 6 | 6 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2868): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0011 | 0/0 | 2879 | 2 | 2 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0013 | 0/0 | 2880 | 2 | 2 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0017 | 0/0 | 2878 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0019 | 0/0 | 2878 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0022 | 0/0 | 2878 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0001c0001t0023 | 0/0 | 2872 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2867): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0001 | 0/0 | 2878 | 18 | 1 | 1 | 15 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0002 | 0/0 | 2879 | 24 | 3 | 7 | 11 | 0 | 3 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0003 | 0/0 | 2880 | 41 | 5 | 14 | 15 | 2 | 5 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0004 | 0/0 | 2880 | 35 | 10 | 6 | 16 | 0 | 3 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0005 | 0/0 | 2877 | 4 | 3 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2872): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0007 | 0/0 | 2880 | 9 | 0 | 2 | 7 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0008 | 0/0 | 2879 | 5 | 0 | 0 | 4 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0010 | 0/0 | 2879 | 5 | 5 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0011 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0012 | 0/0 | 2879 | 3 | 0 | 0 | 3 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0014 | 0/0 | 2879 | 2 | 2 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0020 | 0/0 | 2880 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0021 | 0/0 | 2879 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0024 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0002t0025 | 0/0 | 2880 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0003t0001 | 0/0 | 2878 | 35 | 4 | 13 | 11 | 4 | 3 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0001c0003t0002 | 0/0 | 2879 | 8 | 1 | 1 | 5 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0003t0003 | 0/0 | 2880 | 2 | 0 | 2 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0003t0005 | 0/0 | 2877 | 2 | 0 | 0 | 1 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2872): Show |
chr10 | 116844499 | 116887601 |
| a0001c0003t0006 | 0/0 | 2878 | 16 | 1 | 10 | 0 | 3 | 2 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0001c0003t0015 | 0/0 | 2878 | 2 | 0 | 0 | 0 | 1 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0001c0006t0016 | 0/0 | 2878 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0001c0009t0002 | 0/0 | 2879 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0001c0011t0003 | 0/0 | 2880 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0001c0014t0003 | 0/0 | 2880 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0002c0004t0001 | 0/0 | 2878 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0002c0004t0003 | 0/0 | 2880 | 8 | 0 | 0 | 8 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0003c0013t0007 | 0/0 | 2880 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2875): Show |
chr10 | 116844499 | 116887601 |
| a0004c0015t0002 | 0/0 | 2879 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2874): Show |
chr10 | 116844499 | 116887601 |
| a0005c0010t0002 | 0/0 | 2877 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2872): Show |
chr10 | 116844499 | 116887601 |
| a0006c0008t0001 | 0/0 | 2878 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0007c0005t0001 | 0/0 | 2878 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2873): Show |
chr10 | 116844499 | 116887601 |
| a0008c0012t0004 | 0/0 | 2882 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2877): Show |
chr10 | 116844499 | 116887601 |
| a0009c0007t0002 | 0/0 | 2877 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | GCCTA others(2872): Show |
chr10 | 116844499 | 116887601 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0008g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0009g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0009g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0009g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0009g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0009g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0013g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0013g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0017g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0019g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0022g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0001t0023g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0007g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0008g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0008g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0010g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0010g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0010g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0012g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0012g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0014g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0014g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0020g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0021g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0024g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0002t0025g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0015 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0015g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0003t0015g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0006t0016g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0009t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0011t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0001c0014t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0002c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0002c0004t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0002c0004t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0002c0004t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0002c0004t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0002c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0003c0013t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0004c0015t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0005c0010t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0006c0008t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0007c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0008c0012t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| a0009c0007t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0274 | EUR | GBR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0078 | EUR | GBR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0095 | EUR | GBR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00280 | hp1 | a0001 | c0003 | t0006 | g0195 | EUR | FIN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00323 | hp1 | a0001 | c0003 | t0006 | g0127 | EUR | FIN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00323 | hp2 | a0001 | c0003 | t0006 | g0277 | EUR | FIN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00408 | hp2 | a0002 | c0004 | t0001 | g0110 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00423 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00438 | hp2 | a0001 | c0002 | t0007 | g0101 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00544 | hp2 | a0002 | c0004 | t0003 | g0021 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00558 | hp1 | a0001 | c0003 | t0005 | g0293 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00597 | hp1 | a0001 | c0002 | t0007 | g0001 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0112 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00621 | hp1 | a0002 | c0004 | t0003 | g0021 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0146 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00639 | hp1 | a0001 | c0003 | t0006 | g0126 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00642 | hp2 | a0001 | c0003 | t0006 | g0054 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00673 | hp2 | a0001 | c0002 | t0007 | g0001 | EAS | CHS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00735 | hp2 | a0001 | c0001 | t0023 | g0304 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00738 | hp1 | a0001 | c0002 | t0004 | g0001 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00738 | hp2 | a0001 | c0003 | t0006 | g0279 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0178 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0272 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0287 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01071 | hp1 | a0001 | c0003 | t0003 | g0276 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01071 | hp2 | a0001 | c0014 | t0003 | g0089 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0105 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0086 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0325 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0314 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0278 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01168 | hp1 | a0001 | c0003 | t0006 | g0124 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0254 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0202 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01175 | hp2 | a0001 | c0002 | t0004 | g0074 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0030 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0209 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0177 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0115 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0211 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0131 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01257 | hp1 | a0001 | c0003 | t0006 | g0055 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01257 | hp2 | a0001 | c0003 | t0006 | g0006 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01258 | hp2 | a0001 | c0003 | t0006 | g0053 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0104 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01346 | hp2 | a0001 | c0003 | t0006 | g0006 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0263 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0069 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0083 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0098 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0047 | EUR | IBS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01516 | hp2 | a0001 | c0003 | t0015 | g0275 | EUR | IBS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0048 | EUR | IBS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0251 | EUR | IBS | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0114 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0037 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0312 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0244 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0144 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0324 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01943 | hp1 | a0001 | c0003 | t0006 | g0291 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0142 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01952 | hp1 | a0001 | c0003 | t0006 | g0253 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01978 | hp1 | a0001 | c0002 | t0003 | g0087 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0064 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0143 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0116 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02015 | hp1 | a0003 | c0013 | t0007 | g0099 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02015 | hp2 | a0001 | c0002 | t0004 | g0138 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02027 | hp1 | a0001 | c0003 | t0001 | g0172 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0100 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02040 | hp2 | a0001 | c0001 | t0017 | g0013 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0068 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0057 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0250 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0221 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0050 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0230 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | KHV | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CDX | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CDX | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CDX | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0240 | EAS | CDX | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02257 | hp2 | a0004 | c0015 | t0002 | g0184 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0051 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0176 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02273 | hp1 | a0001 | c0002 | t0004 | g0085 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0141 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02280 | hp2 | a0001 | c0001 | t0019 | g0196 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02293 | hp2 | a0001 | c0002 | t0007 | g0139 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02300 | hp1 | a0001 | c0001 | t0022 | g0215 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0165 | AMR | PEL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0094 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02451 | hp2 | a0001 | c0002 | t0011 | g0130 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02615 | hp1 | a0001 | c0002 | t0014 | g0123 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0315 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0270 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02622 | hp2 | a0001 | c0002 | t0010 | g0134 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0308 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0300 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0088 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0052 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0264 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0045 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0271 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0121 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0303 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0019 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | ESN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0311 | AFR | ESN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03017 | hp1 | a0001 | c0003 | t0015 | g0260 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0259 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0128 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0075 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0280 | AFR | ESN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0037 | AFR | ESN | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0070 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03239 | hp1 | a0001 | c0003 | t0006 | g0258 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03239 | hp2 | a0001 | c0002 | t0021 | g0148 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0307 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03453 | hp2 | a0001 | c0002 | t0004 | g0001 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03486 | hp2 | a0001 | c0002 | t0010 | g0132 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0001 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0310 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0001 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03654 | hp1 | a0001 | c0003 | t0005 | g0229 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03669 | hp1 | a0001 | c0003 | t0006 | g0125 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0210 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | STU | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0152 | SAS | STU | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0067 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0120 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03710 | hp1 | a0005 | c0010 | t0002 | g0072 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0174 | SAS | PJL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0153 | SAS | BEB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0084 | SAS | BEB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0154 | SAS | BEB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03927 | hp2 | a0006 | c0008 | t0001 | g0010 | SAS | BEB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03942 | hp1 | a0001 | c0002 | t0008 | g0056 | SAS | BEB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG04115 | hp1 | a0001 | c0006 | t0016 | g0040 | SAS | STU | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG04115 | hp2 | a0001 | c0002 | t0020 | g0041 | SAS | STU | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0103 | SAS | BEB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0092 | SAS | BEB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG04228 | hp1 | a0001 | c0002 | t0004 | g0071 | SAS | STU | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | CHB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18612 | hp2 | a0001 | c0002 | t0007 | g0022 | EAS | CHB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | CHB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18906 | hp1 | a0001 | c0002 | t0010 | g0133 | AFR | YRI | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | YRI | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0220 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18942 | hp1 | a0001 | c0009 | t0002 | g0241 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18942 | hp2 | a0001 | c0002 | t0004 | g0137 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18945 | hp1 | a0002 | c0004 | t0003 | g0022 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18949 | hp2 | a0001 | c0002 | t0007 | g0066 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0036 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18951 | hp2 | a0001 | c0002 | t0012 | g0001 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18952 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0294 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18959 | hp2 | a0001 | c0002 | t0024 | g0111 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18960 | hp2 | a0001 | c0002 | t0007 | g0102 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18961 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18962 | hp2 | a0001 | c0002 | t0008 | g0002 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18964 | hp1 | a0001 | c0002 | t0012 | g0065 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0296 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0036 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18974 | hp1 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18979 | hp2 | a0001 | c0002 | t0004 | g0136 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18981 | hp1 | a0001 | c0002 | t0008 | g0001 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18984 | hp2 | a0001 | c0002 | t0004 | g0122 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18986 | hp2 | a0001 | c0002 | t0012 | g0001 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18989 | hp2 | a0001 | c0002 | t0025 | g0059 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0205 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18993 | hp1 | a0001 | c0002 | t0005 | g0024 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18994 | hp2 | a0001 | c0002 | t0008 | g0001 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18995 | hp1 | a0002 | c0004 | t0003 | g0119 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18997 | hp2 | a0002 | c0004 | t0003 | g0076 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18998 | hp1 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19004 | hp1 | a0002 | c0004 | t0003 | g0001 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19007 | hp1 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19011 | hp1 | a0001 | c0002 | t0007 | g0108 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19012 | hp2 | a0001 | c0002 | t0004 | g0113 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19030 | hp1 | a0007 | c0005 | t0001 | g0208 | AFR | LWK | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0206 | AFR | LWK | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0109 | AFR | LWK | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19057 | hp1 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19058 | hp1 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19062 | hp2 | a0001 | c0002 | t0008 | g0001 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19063 | hp2 | a0008 | c0012 | t0004 | g0090 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19064 | hp2 | a0001 | c0002 | t0004 | g0149 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19067 | hp2 | a0002 | c0004 | t0003 | g0001 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19072 | hp2 | a0001 | c0003 | t0002 | g0297 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19075 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19075 | hp2 | a0009 | c0007 | t0002 | g0295 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19077 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19079 | hp1 | a0001 | c0011 | t0003 | g0106 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0058 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19083 | hp1 | a0001 | c0002 | t0004 | g0049 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19083 | hp2 | a0002 | c0004 | t0003 | g0001 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0223 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0282 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19089 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19240 | hp1 | a0001 | c0002 | t0014 | g0060 | AFR | YRI | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA19240 | hp2 | a0001 | c0002 | t0010 | g0117 | AFR | YRI | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | ASW | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0269 | EUR | TSI | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0015 | EUR | TSI | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01123 | hp1 | a0001 | c0002 | t0007 | g0001 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0019 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0034 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02559 | hp1 | a0001 | c0002 | t0010 | g0135 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0313 | AFR | ACB | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0034 | AFR | USA | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0212 | AFR | USA | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | USA | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA20300 | hp2 | a0001 | c0003 | t0006 | g0292 | AFR | USA | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | LWK | ENO4_chr10_116844499_116887601 | ENO4 | chr10 | 116844499 | 116887601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:116855645 | C | G | 1 | a0004 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.188C>G | p.Ala63Gly | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 2/14 | 256/2878 | 188/1878 | 63/625 | chr10 | 116855645 | |||
| chr10:116860803 | A | C | 1 | a0006 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.644A>C | p.Asp215Ala | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 5/14 | 712/2878 | 644/1878 | 215/625 | chr10 | 116860803 | |||
| chr10:116860844 | G | A | 1 | a0007 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.685G>A | p.Glu229Lys | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 5/14 | 753/2878 | 685/1878 | 229/625 | chr10 | 116860844 | |||
| chr10:116868666 | CAG | C | 1 | a0005 | 1 | HG03710.hp1 | frameshift_variant | HIGH | c.1011_1012delGA | p.Glu337fs | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/14 | 1079/2878 | 1011/1878 | 337/625 | INFO_REALIGN_3_PRIME | chr10 | 116868666 | ||
| chr10:116871136 | TG | T | 1 | a0009 | 1 | NA19075.hp2 | frameshift_variant | HIGH | c.1061delG | p.Gly354fs | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/14 | 1129/2878 | 1061/1878 | 354/625 | INFO_REALIGN_3_PRIME | chr10 | 116871136 | ||
| chr10:116871164 | AC | A | 1 | a0009 | 1 | NA19075.hp2 | frameshift_variant | HIGH | c.1089delC | p.Ile364fs | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/14 | 1157/2878 | 1089/1878 | 363/625 | INFO_REALIGN_3_PRIME | chr10 | 116871164 | ||
| chr10:116874083 | G | GA | 1 | a0008 | 1 | NA19063.hp2 | frameshift_variant | HIGH | c.1226dupA | p.Tyr410fs | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/14 | 1295/2878 | 1227/1878 | 409/625 | INFO_REALIGN_3_PRIME | chr10 | 116874083 | ||
| chr10:116876094 | C | G | 1 | a0002 | 9 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(6): Show |
missense_variant | MODERATE | c.1371C>G | p.His457Gln | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/14 | 1439/2878 | 1371/1878 | 457/625 | chr10 | 116876094 | |||
| chr10:116876177 | T | TC | 1 | a0008 | 1 | NA19063.hp2 | frameshift_variant | HIGH | c.1458dupC | p.Lys487fs | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/14 | 1527/2878 | 1459/1878 | 487/625 | INFO_REALIGN_3_PRIME | chr10 | 116876177 | ||
| chr10:116879974 | A | G | 1 | a0003 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1711A>G | p.Asn571Asp | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 13/14 | 1779/2878 | 1711/1878 | 571/625 | chr10 | 116879974 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:116856599 | C | T | 7 | a0001c0002 a0001c0011 a0001c0014 others(4): Show |
166 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(163): Show |
synonymous_variant | LOW | c.402C>T | p.Ala134Ala | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/14 | 470/2878 | 402/1878 | 134/625 | chr10 | 116856599 | |||
| chr10:116859092 | A | G | 1 | a0001c0009 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.588A>G | p.Pro196Pro | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/14 | 656/2878 | 588/1878 | 196/625 | chr10 | 116859092 | |||
| chr10:116860948 | A | C | 2 | a0001c0003 a0009c0007 |
66 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
synonymous_variant | LOW | c.789A>C | p.Leu263Leu | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 5/14 | 857/2878 | 789/1878 | 263/625 | chr10 | 116860948 | |||
| chr10:116871196 | G | A | 1 | a0001c0011 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.1119G>A | p.Leu373Leu | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/14 | 1187/2878 | 1119/1878 | 373/625 | chr10 | 116871196 | |||
| chr10:116876094 | C | T | 1 | a0001c0014 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.1371C>T | p.His457His | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/14 | 1439/2878 | 1371/1878 | 457/625 | chr10 | 116876094 | |||
| chr10:116876178 | C | T | 1 | a0001c0006 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.1455C>T | p.Ile485Ile | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/14 | 1523/2878 | 1455/1878 | 485/625 | chr10 | 116876178 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:116849513 | G | A | 1 | a0001c0006t0016 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/14 | 54 | chr10 | 116849513 | ||||||
| chr10:116881885 | G | T | 12 | a0001c0001t0003 a0001c0001t0008 a0001c0002t0003 others(9): Show |
76 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*216G>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 216 | chr10 | 116881885 | ||||||
| chr10:116882154 | A | G | 1 | a0001c0003t0006 | 16 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*485A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 485 | chr10 | 116882154 | ||||||
| chr10:116882214 | CCCTCT | C | 2 | a0001c0001t0009 a0001c0001t0023 |
7 | HG00735.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*549_*553delCTCCT | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 549 | INFO_REALIGN_3_PRIME | chr10 | 116882214 | |||||
| chr10:116882275 | A | T | 1 | a0001c0002t0025 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*606A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 606 | chr10 | 116882275 | ||||||
| chr10:116882365 | T | C | 1 | a0001c0001t0017 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*696T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 696 | chr10 | 116882365 | ||||||
| chr10:116882368 | C | T | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(41): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*699C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 699 | chr10 | 116882368 | ||||||
| chr10:116882397 | A | AT | 2 | a0001c0002t0007 a0003c0013t0007 |
10 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*729dupT | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 730 | INFO_REALIGN_3_PRIME | chr10 | 116882397 | |||||
| chr10:116882398 | T | TA | 12 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0013 others(9): Show |
100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*747dupA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 748 | INFO_REALIGN_3_PRIME | chr10 | 116882398 | |||||
| chr10:116882398 | TA | T | 13 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0017 others(10): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*747delA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 747 | INFO_REALIGN_3_PRIME | chr10 | 116882398 | |||||
| chr10:116882398 | TAA | T | 4 | a0001c0001t0005 a0001c0001t0023 a0001c0002t0005 others(1): Show |
30 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*746_*747delAA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 746 | INFO_REALIGN_3_PRIME | chr10 | 116882398 | |||||
| chr10:116882399 | A | T | 1 | a0001c0002t0024 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*730A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 730 | chr10 | 116882399 | ||||||
| chr10:116882400 | A | T | 1 | a0001c0001t0022 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*731A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 731 | chr10 | 116882400 | ||||||
| chr10:116882417 | T | A | 1 | a0001c0002t0012 | 3 | NA18951.hp2 NA18964.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*748T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 748 | chr10 | 116882417 | ||||||
| chr10:116882444 | G | GC | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(44): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
3_prime_UTR_variant | MODIFIER | c.*776dupC | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 777 | INFO_REALIGN_3_PRIME | chr10 | 116882444 | |||||
| chr10:116882480 | G | A | 1 | a0001c0003t0015 | 2 | HG01516.hp2 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*811G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 811 | chr10 | 116882480 | ||||||
| chr10:116882480 | G | T | 1 | a0001c0002t0014 | 2 | HG02615.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*811G>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 811 | chr10 | 116882480 | ||||||
| chr10:116882483 | T | C | 1 | a0001c0002t0014 | 2 | HG02615.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*814T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 814 | chr10 | 116882483 | ||||||
| chr10:116882545 | T | A | 2 | a0001c0002t0020 a0001c0002t0021 |
2 | HG03239.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*876T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 876 | chr10 | 116882545 | ||||||
| chr10:116882566 | T | G | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(38): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*897T>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 14/14 | 897 | chr10 | 116882566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:116849778 | C | T | 2 | a0001c0002t0003g0324 a0001c0002t0003g0325 |
2 | HG01099.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.165+47C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116849778 | |||||||
| chr10:116849846 | G | A | 1 | a0001c0002t0004g0039 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.165+115G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116849846 | |||||||
| chr10:116849872 | G | A | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+141G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116849872 | |||||||
| chr10:116849874 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.165+143C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116849874 | |||||||
| chr10:116849996 | C | G | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | HG00741.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.165+265C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116849996 | |||||||
| chr10:116850026 | G | C | 1 | a0001c0002t0020g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.165+295G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116850026 | |||||||
| chr10:116850502 | C | T | 2 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.165+771C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116850502 | |||||||
| chr10:116850754 | A | G | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+1023A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116850754 | |||||||
| chr10:116850837 | A | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0316 a0001c0001t0001g0317 others(1): Show |
5 | HG00544.hp1 NA18979.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+1106A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116850837 | |||||||
| chr10:116850859 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.165+1128G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116850859 | |||||||
| chr10:116851103 | C | T | 1 | a0001c0002t0002g0315 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.165+1372C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851103 | |||||||
| chr10:116851148 | C | T | 1 | a0001c0003t0001g0314 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.165+1417C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851148 | |||||||
| chr10:116851282 | G | A | 322 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(319): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.165+1551G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851282 | |||||||
| chr10:116851303 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.165+1572A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851303 | |||||||
| chr10:116851489 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.165+1758G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851489 | |||||||
| chr10:116851507 | G | A | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+1776G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851507 | |||||||
| chr10:116851650 | C | T | 6 | a0001c0003t0002g0036 a0001c0003t0002g0294 a0001c0003t0002g0296 others(3): Show |
7 | HG00558.hp1 NA18951.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+1919C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851650 | |||||||
| chr10:116851682 | G | T | 2 | a0001c0003t0006g0291 a0001c0003t0006g0292 |
2 | HG01943.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.165+1951G>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851682 | |||||||
| chr10:116851824 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0008g0047 a0001c0001t0008g0048 others(1): Show |
4 | HG00099.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+2093T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851824 | |||||||
| chr10:116851886 | T | C | 2 | a0001c0002t0004g0049 a0001c0002t0004g0050 |
2 | HG02129.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.165+2155T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851886 | |||||||
| chr10:116851892 | A | G | 170 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(167): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.165+2161A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851892 | |||||||
| chr10:116851960 | G | C | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+2229G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116851960 | |||||||
| chr10:116852035 | G | A | 1 | a0001c0003t0001g0165 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.165+2304G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116852035 | |||||||
| chr10:116852144 | C | T | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+2413C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116852144 | |||||||
| chr10:116852325 | C | T | 28 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0024 others(25): Show |
34 | HG00609.hp2 HG00621.hp2 HG02083.hp2 others(31): Show |
intron_variant | MODIFIER | c.165+2594C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116852325 | |||||||
| chr10:116852586 | A | G | 8 | a0001c0002t0002g0007 a0001c0002t0002g0141 a0001c0002t0002g0142 others(5): Show |
10 | HG01928.hp1 HG01943.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+2855A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116852586 | |||||||
| chr10:116852720 | A | G | 1 | a0001c0001t0005g0290 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.166-2903A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116852720 | |||||||
| chr10:116852883 | A | C | 2 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.166-2740A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116852883 | |||||||
| chr10:116853021 | C | T | 1 | a0001c0002t0002g0144 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.166-2602C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853021 | |||||||
| chr10:116853023 | C | T | 3 | a0001c0002t0004g0039 a0001c0002t0004g0136 a0001c0002t0004g0137 |
3 | NA18942.hp2 NA18974.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.166-2600C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853023 | |||||||
| chr10:116853080 | G | C | 6 | a0001c0001t0002g0299 a0001c0001t0002g0302 a0001c0001t0005g0298 others(3): Show |
6 | HG01109.hp2 HG02647.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-2543G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853080 | |||||||
| chr10:116853146 | T | A | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.166-2477T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853146 | |||||||
| chr10:116853211 | C | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0035 a0001c0001t0002g0289 |
6 | HG00438.hp1 NA18940.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-2412C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853211 | |||||||
| chr10:116853263 | C | G | 1 | a0001c0001t0004g0288 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.166-2360C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853263 | |||||||
| chr10:116853290 | G | A | 2 | a0001c0002t0005g0051 a0001c0002t0005g0052 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.166-2333G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853290 | |||||||
| chr10:116853294 | C | CA | 161 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(158): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.166-2309dupA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 116853294 | ||||||
| chr10:116853294 | C | CAA | 22 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0002g0166 others(19): Show |
22 | HG00642.hp2 HG00741.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.166-2310_166-2309d others(4): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 116853294 | ||||||
| chr10:116853294 | CA | C | 12 | a0001c0002t0001g0129 a0001c0002t0002g0142 a0001c0002t0002g0143 others(9): Show |
12 | HG01256.hp2 HG01943.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-2309delA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 116853294 | ||||||
| chr10:116853313 | A | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.166-2310A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853313 | |||||||
| chr10:116853511 | A | G | 1 | a0001c0003t0006g0279 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.166-2112A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853511 | |||||||
| chr10:116853764 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.166-1859C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116853764 | |||||||
| chr10:116854244 | G | A | 19 | a0001c0001t0001g0179 a0001c0001t0002g0017 a0001c0001t0002g0026 others(16): Show |
23 | HG00408.hp1 HG00438.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.166-1379G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116854244 | |||||||
| chr10:116854419 | C | T | 178 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(175): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.166-1204C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116854419 | |||||||
| chr10:116854420 | C | T | 137 | a0001c0001t0001g0082 a0001c0001t0002g0319 a0001c0001t0002g0320 others(134): Show |
166 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.166-1203C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116854420 | |||||||
| chr10:116854529 | C | T | 2 | a0001c0003t0001g0178 a0001c0003t0001g0278 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-1094C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116854529 | |||||||
| chr10:116854559 | T | TA | 8 | a0001c0001t0001g0027 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
9 | HG00735.hp1 HG03017.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-1045dupA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 116854559 | ||||||
| chr10:116854559 | TA | T | 183 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0061 others(180): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.166-1045delA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 116854559 | ||||||
| chr10:116854613 | G | A | 1 | a0001c0003t0006g0195 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.166-1010G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116854613 | |||||||
| chr10:116854635 | T | C | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.166-988T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116854635 | |||||||
| chr10:116854748 | G | A | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.166-875G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116854748 | |||||||
| chr10:116854833 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.166-790C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116854833 | |||||||
| chr10:116854940 | C | CA | 19 | a0001c0001t0001g0191 a0001c0001t0001g0197 a0001c0001t0002g0183 others(16): Show |
20 | HG00558.hp1 HG00735.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.166-655dupA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 116854940 | ||||||
| chr10:116854940 | C | CAA | 9 | a0001c0001t0001g0179 a0001c0001t0002g0180 a0001c0001t0002g0181 others(6): Show |
9 | HG01256.hp1 HG01433.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-656_166-655dup others(2): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 116854940 | ||||||
| chr10:116854940 | CA | C | 174 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(171): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.166-655delA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 116854940 | ||||||
| chr10:116854940 | CAA | C | 12 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(9): Show |
12 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-656_166-655del others(2): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | 116854940 | ||||||
| chr10:116855017 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0002g0042 others(1): Show |
4 | HG01109.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-606A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855017 | |||||||
| chr10:116855043 | C | T | 2 | a0001c0003t0001g0015 a0001c0003t0001g0177 |
4 | HG00642.hp1 HG01243.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-580C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855043 | |||||||
| chr10:116855208 | G | T | 1 | a0001c0002t0005g0280 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.166-415G>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855208 | |||||||
| chr10:116855317 | C | A | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.166-306C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855317 | |||||||
| chr10:116855346 | C | A | 9 | a0001c0003t0001g0015 a0001c0003t0001g0165 a0001c0003t0001g0177 others(6): Show |
11 | HG00642.hp1 HG01070.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-277C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855346 | |||||||
| chr10:116855387 | C | T | 337 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(334): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.166-236C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855387 | |||||||
| chr10:116855493 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0193 a0001c0001t0001g0213 others(3): Show |
8 | HG01346.hp1 HG01361.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-130G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855493 | |||||||
| chr10:116855495 | A | G | 1 | a0001c0002t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.166-128A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855495 | |||||||
| chr10:116855511 | C | G | 1 | a0001c0003t0001g0263 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.166-112C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855511 | |||||||
| chr10:116855555 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.166-68T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 1/13 | chr10 | 116855555 | |||||||
| chr10:116855782 | G | A | 1 | a0001c0002t0004g0077 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.294+31G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 2/13 | chr10 | 116855782 | |||||||
| chr10:116855823 | T | C | 1 | a0001c0002t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.294+72T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 2/13 | chr10 | 116855823 | |||||||
| chr10:116855867 | T | G | 1 | a0001c0002t0011g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.294+116T>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 2/13 | chr10 | 116855867 | |||||||
| chr10:116856014 | T | G | 1 | a0001c0001t0002g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.294+263T>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 2/13 | chr10 | 116856014 | |||||||
| chr10:116856056 | G | C | 1 | a0001c0002t0003g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.294+305G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 2/13 | chr10 | 116856056 | |||||||
| chr10:116856193 | A | G | 1 | a0001c0003t0001g0209 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.295-299A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 2/13 | chr10 | 116856193 | |||||||
| chr10:116856697 | T | C | 1 | a0001c0002t0007g0139 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.485+15T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116856697 | |||||||
| chr10:116856724 | G | A | 1 | a0001c0002t0002g0008 | 3 | NA19007.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.485+42G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116856724 | |||||||
| chr10:116856767 | C | T | 1 | a0001c0002t0003g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.485+85C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116856767 | |||||||
| chr10:116856793 | A | C | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.485+111A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116856793 | |||||||
| chr10:116856882 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0218 others(3): Show |
9 | HG00280.hp2 HG01099.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.485+200G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116856882 | |||||||
| chr10:116856968 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.485+286G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116856968 | |||||||
| chr10:116856988 | C | CA | 7 | a0001c0001t0001g0222 a0001c0001t0001g0281 a0001c0001t0003g0198 others(4): Show |
7 | HG00735.hp1 HG02027.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+322dupA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 116856988 | ||||||
| chr10:116856988 | CA | C | 142 | a0001c0001t0009g0037 a0001c0001t0009g0310 a0001c0001t0009g0311 others(139): Show |
173 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.485+322delA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 116856988 | ||||||
| chr10:116856991 | A | G | 136 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0024 others(133): Show |
166 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.485+309A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116856991 | |||||||
| chr10:116857003 | A | T | 1 | a0002c0004t0003g0119 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.485+321A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857003 | |||||||
| chr10:116857026 | G | A | 136 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0024 others(133): Show |
166 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.485+344G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857026 | |||||||
| chr10:116857103 | C | T | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.485+421C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857103 | |||||||
| chr10:116857152 | A | T | 36 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(33): Show |
42 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+470A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857152 | |||||||
| chr10:116857217 | G | C | 1 | a0001c0002t0007g0139 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.485+535G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857217 | |||||||
| chr10:116857426 | A | G | 1 | a0001c0001t0004g0189 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.485+744A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857426 | |||||||
| chr10:116857642 | C | CT | 152 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(149): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.485+974dupT | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 116857642 | ||||||
| chr10:116857675 | G | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG04228.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.485+993G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857675 | |||||||
| chr10:116857750 | T | C | 139 | a0001c0001t0003g0171 a0001c0001t0003g0198 a0001c0001t0005g0201 others(136): Show |
169 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.485+1068T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857750 | |||||||
| chr10:116857806 | T | C | 10 | a0001c0001t0001g0061 a0001c0001t0002g0042 a0001c0001t0002g0319 others(7): Show |
11 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.485+1124T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857806 | |||||||
| chr10:116857928 | C | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0035 a0001c0001t0002g0289 |
6 | HG00438.hp1 NA18940.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-1062C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116857928 | |||||||
| chr10:116858155 | A | G | 2 | a0001c0003t0003g0276 a0001c0003t0003g0287 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.486-835A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116858155 | |||||||
| chr10:116858464 | GT | G | 83 | a0001c0002t0001g0093 a0001c0002t0002g0075 a0001c0002t0002g0088 others(80): Show |
105 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.486-520delT | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | 116858464 | ||||||
| chr10:116858466 | T | A | 2 | a0001c0001t0002g0299 a0001c0001t0002g0302 |
2 | HG01109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.486-524T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116858466 | |||||||
| chr10:116858652 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0227 a0001c0001t0002g0028 others(1): Show |
4 | NA18948.hp2 NA18983.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-338G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116858652 | |||||||
| chr10:116858733 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0005g0200 a0007c0005t0001g0208 |
3 | HG02145.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.486-257C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116858733 | |||||||
| chr10:116858826 | G | A | 1 | a0001c0001t0013g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.486-164G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 3/13 | chr10 | 116858826 | |||||||
| chr10:116859297 | T | C | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.634+159T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116859297 | |||||||
| chr10:116859300 | C | T | 1 | a0001c0002t0021g0148 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.634+162C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116859300 | |||||||
| chr10:116859657 | G | A | 1 | a0001c0002t0003g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.634+519G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116859657 | |||||||
| chr10:116859824 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.634+686A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116859824 | |||||||
| chr10:116860018 | G | A | 148 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(145): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.635-776G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860018 | |||||||
| chr10:116860148 | A | C | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.635-646A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860148 | |||||||
| chr10:116860151 | C | T | 6 | a0001c0001t0009g0037 a0001c0001t0009g0310 a0001c0001t0009g0311 others(3): Show |
7 | HG00735.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-643C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860151 | |||||||
| chr10:116860207 | C | A | 2 | a0001c0002t0004g0049 a0001c0002t0004g0050 |
2 | HG02129.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.635-587C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860207 | |||||||
| chr10:116860272 | A | G | 136 | a0001c0001t0003g0171 a0001c0001t0003g0198 a0001c0001t0005g0201 others(133): Show |
165 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.635-522A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860272 | |||||||
| chr10:116860317 | G | A | 1 | a0001c0001t0002g0183 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.635-477G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860317 | |||||||
| chr10:116860423 | G | A | 84 | a0001c0001t0003g0171 a0001c0001t0003g0198 a0001c0002t0001g0093 others(81): Show |
106 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.635-371G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860423 | |||||||
| chr10:116860446 | C | A | 327 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(324): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.635-348C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860446 | |||||||
| chr10:116860617 | A | G | 2 | a0001c0003t0015g0260 a0001c0003t0015g0275 |
2 | HG01516.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.635-177A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860617 | |||||||
| chr10:116860651 | G | C | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.635-143G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 4/13 | chr10 | 116860651 | |||||||
| chr10:116861221 | TA | T | 27 | a0001c0001t0001g0179 a0001c0001t0001g0322 a0001c0001t0002g0017 others(24): Show |
32 | HG00408.hp1 HG00438.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.936+47delA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 116861221 | ||||||
| chr10:116861221 | TAA | T | 138 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(135): Show |
159 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.936+46_936+47delAA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 116861221 | ||||||
| chr10:116861221 | TAAA | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0005g0284 others(5): Show |
10 | HG02145.hp2 HG02258.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.936+45_936+47delAA others(1): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 116861221 | ||||||
| chr10:116861234 | A | T | 4 | a0001c0001t0002g0167 a0001c0002t0003g0078 a0001c0002t0003g0116 others(1): Show |
4 | HG00140.hp1 HG01993.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+44A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861234 | |||||||
| chr10:116861235 | AAAT | A | 15 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0062 others(12): Show |
17 | HG00639.hp2 HG01258.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.936+47_936+49delAT others(1): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 116861235 | ||||||
| chr10:116861236 | A | AAT | 68 | a0001c0001t0003g0171 a0001c0001t0003g0198 a0001c0001t0009g0312 others(65): Show |
93 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.936+66_936+67dupTA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 116861236 | ||||||
| chr10:116861236 | A | AATAT | 7 | a0001c0002t0003g0104 a0001c0002t0003g0105 a0001c0002t0003g0107 others(4): Show |
7 | HG01081.hp1 HG01175.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.936+64_936+67dupTA others(2): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 116861236 | ||||||
| chr10:116861236 | A | AT | 4 | a0001c0002t0004g0109 a0001c0002t0024g0111 a0002c0004t0001g0110 others(1): Show |
5 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.936+46_936+47insT | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861236 | |||||||
| chr10:116861236 | A | ATAT | 4 | a0001c0002t0002g0075 a0001c0002t0003g0083 a0001c0002t0003g0112 others(1): Show |
4 | HG00609.hp1 HG01433.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+46_936+47insTA others(1): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861236 | |||||||
| chr10:116861236 | A | T | 40 | a0001c0001t0001g0046 a0001c0001t0001g0179 a0001c0001t0001g0256 others(37): Show |
45 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.936+46A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861236 | |||||||
| chr10:116861237 | AT | A | 15 | a0001c0001t0004g0309 a0001c0002t0001g0063 a0001c0002t0001g0129 others(12): Show |
15 | HG01109.hp1 HG02258.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.936+48delT | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861237 | |||||||
| chr10:116861238 | T | A | 5 | a0001c0001t0009g0310 a0001c0002t0002g0150 a0001c0002t0002g0151 others(2): Show |
5 | HG01433.hp1 HG02055.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.936+48T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861238 | |||||||
| chr10:116861240 | T | A | 2 | a0001c0002t0010g0117 a0001c0002t0010g0132 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.936+50T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861240 | |||||||
| chr10:116861242 | T | A | 1 | a0001c0002t0010g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.936+52T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861242 | |||||||
| chr10:116861266 | T | C | 137 | a0001c0001t0003g0171 a0001c0001t0003g0198 a0001c0002t0001g0004 others(134): Show |
167 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.936+76T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861266 | |||||||
| chr10:116861362 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.936+172C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861362 | |||||||
| chr10:116861485 | G | A | 137 | a0001c0001t0003g0171 a0001c0001t0003g0198 a0001c0002t0001g0004 others(134): Show |
167 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.936+295G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861485 | |||||||
| chr10:116861738 | A | G | 1 | a0001c0002t0002g0008 | 3 | NA19007.hp2 NA19012.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.936+548A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861738 | |||||||
| chr10:116861769 | G | A | 1 | a0001c0002t0002g0141 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.936+579G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861769 | |||||||
| chr10:116861886 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0005g0201 |
2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.936+696T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861886 | |||||||
| chr10:116861953 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0281 a0001c0001t0001g0283 others(1): Show |
4 | HG00639.hp2 HG00735.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+763G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116861953 | |||||||
| chr10:116862023 | G | A | 3 | a0001c0002t0003g0086 a0001c0002t0003g0087 a0001c0002t0003g0104 |
3 | HG01081.hp2 HG01261.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.937-776G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862023 | |||||||
| chr10:116862158 | T | C | 1 | a0001c0003t0006g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.937-641T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862158 | |||||||
| chr10:116862250 | G | A | 3 | a0001c0002t0003g0034 a0001c0002t0003g0270 a0001c0002t0003g0271 |
4 | HG02109.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.937-549G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862250 | |||||||
| chr10:116862262 | G | A | 1 | a0001c0002t0002g0118 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.937-537G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862262 | |||||||
| chr10:116862263 | A | C | 1 | a0001c0001t0001g0062 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.937-536A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862263 | |||||||
| chr10:116862399 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.937-400G>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862399 | |||||||
| chr10:116862428 | G | T | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.937-371G>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862428 | |||||||
| chr10:116862460 | CA | C | 34 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0061 others(31): Show |
39 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.937-328delA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr10 | 116862460 | ||||||
| chr10:116862466 | A | T | 1 | a0001c0002t0010g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.937-333A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862466 | |||||||
| chr10:116862617 | A | T | 156 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(153): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.937-182A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862617 | |||||||
| chr10:116862640 | C | A | 1 | a0001c0003t0005g0229 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.937-159C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862640 | |||||||
| chr10:116862728 | C | A | 1 | a0001c0003t0001g0314 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.937-71C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862728 | |||||||
| chr10:116862729 | G | A | 4 | a0001c0001t0005g0298 a0001c0001t0005g0300 a0001c0001t0005g0301 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-70G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862729 | |||||||
| chr10:116862785 | T | G | 1 | a0001c0003t0001g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.937-14T>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 6/13 | chr10 | 116862785 | |||||||
| chr10:116863057 | A | C | 5 | a0001c0002t0007g0066 a0001c0002t0007g0101 a0001c0002t0007g0102 others(2): Show |
5 | HG00438.hp2 NA18949.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.990+205A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863057 | |||||||
| chr10:116863058 | A | G | 1 | a0001c0001t0004g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.990+206A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863058 | |||||||
| chr10:116863164 | G | C | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.990+312G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863164 | |||||||
| chr10:116863170 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.990+318C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863170 | |||||||
| chr10:116863176 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.990+324C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863176 | |||||||
| chr10:116863356 | T | TCA | 33 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0179 others(30): Show |
38 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.990+534_990+535dup others(2): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116863356 | ||||||
| chr10:116863356 | T | TCACA | 118 | a0001c0001t0001g0038 a0001c0001t0001g0062 a0001c0001t0001g0316 others(115): Show |
147 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.990+532_990+535dup others(4): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116863356 | ||||||
| chr10:116863356 | T | TCACACA | 118 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(115): Show |
136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.990+530_990+535dup others(6): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116863356 | ||||||
| chr10:116863356 | T | TCACACAC others(1): Show |
29 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0082 others(26): Show |
36 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.990+528_990+535dup others(8): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116863356 | ||||||
| chr10:116863356 | T | TCACACAC others(3): Show |
16 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0005g0169 others(13): Show |
16 | HG00639.hp2 HG01106.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.990+526_990+535dup others(10): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116863356 | ||||||
| chr10:116863356 | T | TCACACAC others(5): Show |
3 | a0001c0002t0003g0087 a0001c0002t0003g0104 a0001c0002t0004g0085 |
3 | HG01261.hp2 HG01978.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.990+524_990+535dup others(12): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116863356 | ||||||
| chr10:116863356 | T | TCACACAC others(7): Show |
1 | a0001c0001t0001g0266 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.990+522_990+535dup others(14): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116863356 | ||||||
| chr10:116863356 | TCA | T | 4 | a0001c0001t0013g0307 a0001c0001t0013g0308 a0001c0002t0003g0020 others(1): Show |
5 | HG02040.hp1 HG02647.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.990+534_990+535del others(2): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116863356 | ||||||
| chr10:116863376 | A | G | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.990+524A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863376 | |||||||
| chr10:116863637 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.990+785G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863637 | |||||||
| chr10:116863643 | G | A | 34 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0024 others(31): Show |
42 | HG00609.hp2 HG00621.hp2 HG01928.hp1 others(39): Show |
intron_variant | MODIFIER | c.990+791G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863643 | |||||||
| chr10:116863756 | C | T | 1 | a0001c0002t0002g0144 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.990+904C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863756 | |||||||
| chr10:116863811 | C | T | 134 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0024 others(131): Show |
164 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.990+959C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863811 | |||||||
| chr10:116863911 | GCTCTGAT others(6): Show |
G | 2 | a0001c0001t0001g0061 a0001c0001t0002g0042 |
2 | HG01243.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.990+1065_990+1077d others(15): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116863911 | ||||||
| chr10:116863953 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.990+1101C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116863953 | |||||||
| chr10:116864068 | C | T | 2 | a0001c0001t0011g0176 a0001c0001t0011g0206 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.990+1216C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864068 | |||||||
| chr10:116864069 | G | A | 2 | a0001c0001t0013g0307 a0001c0001t0013g0308 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.990+1217G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864069 | |||||||
| chr10:116864488 | A | T | 1 | a0001c0003t0001g0254 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.990+1636A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864488 | |||||||
| chr10:116864489 | A | T | 325 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(322): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.990+1637A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864489 | |||||||
| chr10:116864548 | T | C | 2 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.990+1696T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864548 | |||||||
| chr10:116864682 | C | A | 1 | a0001c0002t0001g0158 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.990+1830C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864682 | |||||||
| chr10:116864683 | C | T | 1 | a0007c0005t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.990+1831C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864683 | |||||||
| chr10:116864717 | A | T | 135 | a0001c0001t0003g0171 a0001c0001t0003g0198 a0001c0002t0001g0004 others(132): Show |
165 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.990+1865A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864717 | |||||||
| chr10:116864718 | A | T | 1 | a0008c0012t0004g0090 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.990+1866A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864718 | |||||||
| chr10:116864768 | C | T | 4 | a0001c0002t0003g0128 a0001c0002t0005g0051 a0001c0002t0005g0052 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+1916C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864768 | |||||||
| chr10:116864790 | C | T | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.990+1938C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864790 | |||||||
| chr10:116864803 | T | G | 4 | a0001c0002t0003g0086 a0001c0002t0003g0087 a0001c0002t0003g0104 others(1): Show |
4 | HG01081.hp2 HG01261.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+1951T>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864803 | |||||||
| chr10:116864912 | C | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0035 a0001c0001t0002g0289 |
6 | HG00438.hp1 NA18940.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.990+2060C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116864912 | |||||||
| chr10:116865052 | A | G | 1 | a0001c0002t0003g0107 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.990+2200A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116865052 | |||||||
| chr10:116865115 | GC | G | 10 | a0001c0001t0001g0061 a0001c0001t0002g0042 a0001c0001t0002g0319 others(7): Show |
11 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.990+2266delC | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116865115 | ||||||
| chr10:116865256 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.990+2404C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116865256 | |||||||
| chr10:116865265 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.990+2413G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116865265 | |||||||
| chr10:116865437 | G | A | 1 | a0001c0001t0005g0230 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.990+2585G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116865437 | |||||||
| chr10:116865513 | C | A | 1 | a0001c0002t0004g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.990+2661C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116865513 | |||||||
| chr10:116865572 | T | A | 1 | a0009c0007t0002g0295 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.990+2720T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116865572 | |||||||
| chr10:116865681 | T | C | 337 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(334): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.990+2829T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116865681 | |||||||
| chr10:116865707 | C | T | 5 | a0001c0001t0001g0197 a0001c0001t0002g0319 a0001c0001t0002g0320 others(2): Show |
5 | HG02145.hp1 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.990+2855C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116865707 | |||||||
| chr10:116865860 | G | C | 1 | a0001c0003t0001g0269 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.991-2790G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116865860 | |||||||
| chr10:116866068 | A | T | 1 | a0001c0001t0004g0288 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.991-2582A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116866068 | |||||||
| chr10:116866143 | A | G | 139 | a0001c0001t0003g0171 a0001c0001t0003g0198 a0001c0001t0005g0201 others(136): Show |
169 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.991-2507A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116866143 | |||||||
| chr10:116866230 | C | T | 1 | a0001c0002t0014g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.991-2420C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116866230 | |||||||
| chr10:116866365 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0004g0309 |
3 | HG02809.hp2 HG02965.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.991-2285A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116866365 | |||||||
| chr10:116866563 | C | T | 1 | a0001c0001t0005g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.991-2087C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116866563 | |||||||
| chr10:116866722 | T | C | 1 | a0001c0002t0002g0118 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.991-1928T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116866722 | |||||||
| chr10:116867059 | A | T | 1 | a0001c0003t0006g0253 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.991-1591A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867059 | |||||||
| chr10:116867184 | G | A | 3 | a0001c0002t0003g0140 a0001c0002t0003g0324 a0001c0002t0003g0325 |
3 | HG01099.hp2 HG01928.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.991-1466G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867184 | |||||||
| chr10:116867224 | C | G | 4 | a0001c0001t0005g0298 a0001c0001t0005g0300 a0001c0001t0005g0301 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-1426C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867224 | |||||||
| chr10:116867264 | C | G | 1 | a0001c0002t0014g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.991-1386C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867264 | |||||||
| chr10:116867421 | C | CA | 113 | a0001c0001t0001g0216 a0001c0001t0002g0017 a0001c0001t0002g0035 others(110): Show |
138 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.991-1211dupA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116867421 | ||||||
| chr10:116867421 | C | CAA | 156 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(153): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.991-1212_991-1211d others(4): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr10 | 116867421 | ||||||
| chr10:116867440 | T | A | 1 | a0008c0012t0004g0090 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.991-1210T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867440 | |||||||
| chr10:116867657 | A | G | 1 | a0001c0003t0001g0251 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.991-993A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867657 | |||||||
| chr10:116867660 | T | C | 3 | a0001c0002t0001g0129 a0001c0002t0014g0060 a0001c0002t0014g0123 |
3 | HG02615.hp1 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.991-990T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867660 | |||||||
| chr10:116867695 | G | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0190 |
2 | NA18948.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.991-955G>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867695 | |||||||
| chr10:116867947 | T | C | 1 | a0001c0002t0004g0146 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.991-703T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867947 | |||||||
| chr10:116867996 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.991-654A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116867996 | |||||||
| chr10:116868138 | A | T | 1 | a0008c0012t0004g0090 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.991-512A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116868138 | |||||||
| chr10:116868221 | G | A | 1 | a0001c0003t0001g0211 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.991-429G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116868221 | |||||||
| chr10:116868244 | C | T | 1 | a0001c0002t0014g0123 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.991-406C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116868244 | |||||||
| chr10:116868282 | T | G | 1 | a0001c0003t0001g0231 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.991-368T>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116868282 | |||||||
| chr10:116868515 | G | A | 4 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(1): Show |
4 | HG01433.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.991-135G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116868515 | |||||||
| chr10:116868525 | G | A | 154 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(151): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.991-125G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116868525 | |||||||
| chr10:116868541 | G | A | 1 | a0001c0002t0002g0118 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.991-109G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116868541 | |||||||
| chr10:116868636 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.991-14C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 7/13 | chr10 | 116868636 | |||||||
| chr10:116868857 | C | G | 1 | a0001c0002t0004g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1047+151C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116868857 | |||||||
| chr10:116868874 | C | A | 154 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(151): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1047+168C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116868874 | |||||||
| chr10:116869284 | G | T | 332 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(329): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1047+578G>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116869284 | |||||||
| chr10:116869411 | C | T | 5 | a0001c0002t0010g0132 a0001c0002t0010g0133 a0001c0002t0010g0134 others(2): Show |
5 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047+705C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116869411 | |||||||
| chr10:116869536 | C | G | 1 | a0003c0013t0007g0099 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1047+830C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116869536 | |||||||
| chr10:116869646 | G | A | 3 | a0001c0001t0005g0298 a0001c0001t0005g0301 a0001c0001t0005g0303 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1047+940G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116869646 | |||||||
| chr10:116869765 | AC | A | 99 | a0001c0002t0001g0093 a0001c0002t0001g0129 a0001c0002t0002g0075 others(96): Show |
121 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1047+1060delC | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116869765 | |||||||
| chr10:116869894 | G | A | 1 | a0007c0005t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1047+1188G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116869894 | |||||||
| chr10:116869907 | C | CATA | 337 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(334): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.1047+1205_1047+120 others(7): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 116869907 | ||||||
| chr10:116869938 | T | C | 58 | a0001c0001t0002g0017 a0001c0001t0002g0026 a0001c0001t0002g0033 others(55): Show |
71 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1048-1187T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116869938 | |||||||
| chr10:116870104 | A | C | 1 | a0001c0003t0005g0229 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1048-1021A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116870104 | |||||||
| chr10:116870582 | C | A | 1 | a0001c0002t0014g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1048-543C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116870582 | |||||||
| chr10:116870610 | A | G | 3 | a0001c0001t0013g0307 a0001c0001t0013g0308 a0001c0006t0016g0040 |
3 | HG02647.hp1 HG03453.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1048-515A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116870610 | |||||||
| chr10:116870663 | TCTC | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0218 |
4 | HG00280.hp2 HG01099.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048-459_1048-457d others(5): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr10 | 116870663 | ||||||
| chr10:116870980 | A | G | 1 | a0001c0002t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1048-145A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116870980 | |||||||
| chr10:116871007 | G | C | 1 | a0001c0003t0005g0293 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1048-118G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116871007 | |||||||
| chr10:116871066 | A | G | 1 | a0001c0002t0003g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1048-59A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 8/13 | chr10 | 116871066 | |||||||
| chr10:116871318 | C | A | 4 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(1): Show |
4 | HG02257.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+26C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116871318 | |||||||
| chr10:116871594 | A | C | 7 | a0001c0002t0002g0007 a0001c0002t0002g0141 a0001c0002t0002g0142 others(4): Show |
9 | HG01928.hp1 HG01943.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215+302A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116871594 | |||||||
| chr10:116871831 | C | T | 336 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(333): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.1215+539C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116871831 | |||||||
| chr10:116871883 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1215+591G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116871883 | |||||||
| chr10:116871970 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1215+678G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116871970 | |||||||
| chr10:116872049 | T | C | 8 | a0001c0001t0001g0173 a0001c0001t0001g0194 a0001c0001t0001g0281 others(5): Show |
8 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1215+757T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872049 | |||||||
| chr10:116872058 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1215+766G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872058 | |||||||
| chr10:116872061 | G | A | 2 | a0001c0001t0003g0187 a0001c0001t0003g0262 |
2 | HG00673.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1215+769G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872061 | |||||||
| chr10:116872197 | C | G | 1 | a0001c0003t0001g0254 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1215+905C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872197 | |||||||
| chr10:116872353 | A | T | 1 | a0009c0007t0002g0295 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1215+1061A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872353 | |||||||
| chr10:116872364 | G | C | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1215+1072G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872364 | |||||||
| chr10:116872533 | T | C | 6 | a0001c0002t0010g0117 a0001c0002t0010g0132 a0001c0002t0010g0133 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+1241T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872533 | |||||||
| chr10:116872596 | A | T | 1 | a0001c0001t0001g0032 | 2 | HG02083.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1215+1304A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872596 | |||||||
| chr10:116872628 | C | A | 2 | a0001c0001t0013g0307 a0001c0001t0013g0308 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1215+1336C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872628 | |||||||
| chr10:116872696 | C | A | 1 | a0001c0003t0001g0240 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1216-1380C>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872696 | |||||||
| chr10:116872730 | A | G | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1216-1346A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872730 | |||||||
| chr10:116872769 | G | A | 1 | a0001c0002t0003g0091 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1216-1307G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872769 | |||||||
| chr10:116872905 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0193 others(9): Show |
15 | HG01346.hp1 HG01361.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1216-1171C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116872905 | |||||||
| chr10:116872976 | TA | T | 5 | a0001c0001t0002g0180 a0001c0003t0001g0031 a0001c0003t0001g0205 others(2): Show |
6 | HG02818.hp2 HG04115.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216-1090delA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr10 | 116872976 | ||||||
| chr10:116873107 | T | G | 1 | a0001c0003t0001g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1216-969T>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116873107 | |||||||
| chr10:116873139 | G | A | 1 | a0001c0002t0004g0109 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1216-937G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116873139 | |||||||
| chr10:116873303 | C | T | 5 | a0001c0001t0001g0173 a0001c0001t0001g0194 a0001c0001t0001g0281 others(2): Show |
5 | HG00639.hp2 HG00735.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-773C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116873303 | |||||||
| chr10:116873401 | T | A | 1 | a0009c0007t0002g0295 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1216-675T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116873401 | |||||||
| chr10:116873634 | G | T | 337 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(334): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.1216-442G>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116873634 | |||||||
| chr10:116873723 | C | G | 1 | a0001c0002t0001g0129 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1216-353C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116873723 | |||||||
| chr10:116873857 | C | T | 5 | a0001c0003t0001g0031 a0001c0003t0001g0205 a0001c0003t0001g0223 others(2): Show |
6 | HG02071.hp2 HG02165.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1216-219C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116873857 | |||||||
| chr10:116873966 | G | A | 1 | a0001c0002t0003g0092 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1216-110G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116873966 | |||||||
| chr10:116874010 | G | A | 2 | a0001c0003t0001g0202 a0001c0006t0016g0040 |
2 | HG01175.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1216-66G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116874010 | |||||||
| chr10:116874037 | A | G | 337 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(334): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.1216-39A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 9/13 | chr10 | 116874037 | |||||||
| chr10:116874614 | T | C | 2 | a0001c0001t0013g0307 a0001c0001t0013g0308 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1341+413T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116874614 | |||||||
| chr10:116874846 | G | A | 1 | a0001c0001t0013g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1341+645G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116874846 | |||||||
| chr10:116874871 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1341+670G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116874871 | |||||||
| chr10:116875185 | A | G | 1 | a0001c0002t0010g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1342-880A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116875185 | |||||||
| chr10:116875208 | G | A | 2 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1342-857G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116875208 | |||||||
| chr10:116875223 | T | G | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1342-842T>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116875223 | |||||||
| chr10:116875561 | T | TCACACAC others(1): Show |
13 | a0001c0001t0001g0218 a0001c0001t0001g0239 a0001c0001t0001g0323 others(10): Show |
14 | HG00735.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1342-485_1342-478d others(10): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0199 a0001c0001t0001g0249 a0001c0003t0001g0205 |
3 | NA18988.hp2 NA18992.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1342-487_1342-478d others(12): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | T | TCACACAC others(5): Show |
147 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(144): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1342-489_1342-478d others(14): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | T | TCACACAC others(7): Show |
25 | a0001c0001t0001g0173 a0001c0001t0001g0179 a0001c0001t0001g0256 others(22): Show |
26 | HG00642.hp2 HG00735.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1342-491_1342-478d others(16): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | T | TCACACAC others(9): Show |
12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0285 others(9): Show |
12 | HG00639.hp2 HG01123.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1342-493_1342-478d others(18): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | T | TCACACAC others(11): Show |
30 | a0001c0001t0001g0283 a0001c0001t0001g0316 a0001c0001t0002g0042 others(27): Show |
36 | HG00609.hp2 HG00621.hp2 HG01928.hp1 others(33): Show |
intron_variant | MODIFIER | c.1342-495_1342-478d others(20): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | T | TCACACAC others(13): Show |
3 | a0001c0002t0001g0160 a0001c0002t0010g0117 a0001c0002t0010g0132 |
3 | HG03486.hp2 NA18945.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1342-497_1342-478d others(22): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | T | TCACACAC others(15): Show |
3 | a0001c0002t0002g0008 a0001c0002t0002g0157 a0001c0002t0010g0133 |
5 | NA18906.hp1 NA18944.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1342-499_1342-478d others(24): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | T | TCTCACAC others(7): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1342-503_1342-502i others(16): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | TCA | T | 91 | a0001c0001t0003g0171 a0001c0001t0003g0198 a0001c0002t0001g0093 others(88): Show |
113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1342-479_1342-478d others(4): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875561 | TCACACAC others(7): Show |
T | 1 | a0001c0001t0001g0016 | 3 | HG02602.hp2 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1342-491_1342-478d others(16): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr10 | 116875561 | ||||||
| chr10:116875588 | T | C | 17 | a0001c0001t0001g0237 a0001c0001t0001g0243 a0001c0001t0001g0267 others(14): Show |
17 | HG02074.hp2 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1342-477T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116875588 | |||||||
| chr10:116875697 | T | C | 2 | a0001c0002t0001g0024 a0001c0002t0005g0024 |
2 | NA18985.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1342-368T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116875697 | |||||||
| chr10:116875935 | A | G | 1 | a0001c0002t0002g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1342-130A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116875935 | |||||||
| chr10:116875961 | A | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1342-104A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 10/13 | chr10 | 116875961 | |||||||
| chr10:116876351 | T | C | 1 | a0001c0002t0005g0051 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1537+91T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116876351 | |||||||
| chr10:116876441 | A | G | 1 | a0001c0002t0003g0271 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1537+181A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116876441 | |||||||
| chr10:116876475 | C | T | 10 | a0001c0001t0001g0061 a0001c0001t0002g0042 a0001c0001t0002g0319 others(7): Show |
11 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1537+215C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116876475 | |||||||
| chr10:116876595 | C | T | 12 | a0001c0002t0001g0129 a0001c0002t0005g0051 a0001c0002t0005g0052 others(9): Show |
12 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1537+335C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116876595 | |||||||
| chr10:116876672 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1537+412C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116876672 | |||||||
| chr10:116876673 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1537+413G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116876673 | |||||||
| chr10:116876725 | C | T | 4 | a0001c0002t0004g0068 a0001c0002t0004g0069 a0001c0002t0004g0070 others(1): Show |
4 | HG01433.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537+465C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116876725 | |||||||
| chr10:116876950 | AAATT | A | 13 | a0001c0002t0001g0129 a0001c0002t0005g0051 a0001c0002t0005g0052 others(10): Show |
13 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1537+715_1537+718d others(6): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr10 | 116876950 | ||||||
| chr10:116876959 | A | C | 9 | a0001c0001t0001g0199 a0001c0001t0001g0204 a0001c0001t0001g0247 others(6): Show |
9 | NA18941.hp2 NA18954.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.1537+699A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116876959 | |||||||
| chr10:116876979 | T | A | 1 | a0001c0002t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1537+719T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116876979 | |||||||
| chr10:116877156 | C | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0197 a0001c0001t0005g0201 others(1): Show |
4 | HG02886.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537+896C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116877156 | |||||||
| chr10:116877178 | CAT | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0191 a0001c0001t0001g0207 |
4 | HG02572.hp2 HG03471.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537+919_1537+920d others(4): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116877178 | |||||||
| chr10:116877219 | C | T | 2 | a0001c0001t0005g0169 a0001c0001t0005g0290 |
2 | NA19068.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1537+959C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116877219 | |||||||
| chr10:116877223 | C | T | 1 | a0001c0002t0002g0118 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1537+963C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116877223 | |||||||
| chr10:116877310 | A | G | 1 | a0001c0006t0016g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1537+1050A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116877310 | |||||||
| chr10:116877734 | G | C | 1 | a0001c0002t0004g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1537+1474G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116877734 | |||||||
| chr10:116877895 | T | C | 2 | a0001c0001t0013g0307 a0001c0001t0013g0308 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1538-1396T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116877895 | |||||||
| chr10:116877945 | G | A | 5 | a0001c0002t0001g0023 a0001c0002t0001g0156 a0001c0002t0001g0159 others(2): Show |
6 | NA18974.hp2 NA18991.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.1538-1346G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116877945 | |||||||
| chr10:116878298 | G | A | 41 | a0001c0001t0001g0179 a0001c0001t0001g0228 a0001c0003t0001g0015 others(38): Show |
45 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1538-993G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878298 | |||||||
| chr10:116878383 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1538-908G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878383 | |||||||
| chr10:116878565 | C | T | 3 | a0001c0003t0006g0125 a0001c0003t0006g0126 a0001c0003t0006g0127 |
3 | HG00323.hp1 HG00639.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1538-726C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878565 | |||||||
| chr10:116878665 | G | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(165): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1538-626G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878665 | |||||||
| chr10:116878671 | A | G | 66 | a0001c0001t0001g0227 a0001c0001t0001g0243 a0001c0001t0002g0017 others(63): Show |
77 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1538-620A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878671 | |||||||
| chr10:116878707 | TAATAA | T | 149 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(146): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1538-578_1538-574d others(7): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr10 | 116878707 | ||||||
| chr10:116878742 | C | CT | 91 | a0001c0001t0001g0061 a0001c0001t0001g0213 a0001c0001t0001g0243 others(88): Show |
117 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1538-531dupT | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr10 | 116878742 | ||||||
| chr10:116878742 | C | CTT | 71 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
85 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1538-532_1538-531d others(4): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr10 | 116878742 | ||||||
| chr10:116878742 | C | CTTT | 104 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(101): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1538-533_1538-531d others(5): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr10 | 116878742 | ||||||
| chr10:116878742 | C | CTTTT | 47 | a0001c0001t0001g0173 a0001c0001t0001g0266 a0001c0001t0001g0281 others(44): Show |
53 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1538-534_1538-531d others(6): Show |
ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr10 | 116878742 | ||||||
| chr10:116878742 | CT | C | 7 | a0001c0001t0001g0044 a0001c0002t0010g0132 a0001c0002t0010g0133 others(4): Show |
7 | HG02559.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-531delT | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr10 | 116878742 | ||||||
| chr10:116878765 | C | T | 11 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0025 others(8): Show |
15 | HG00609.hp2 HG02083.hp2 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.1538-526C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878765 | |||||||
| chr10:116878773 | T | C | 3 | a0001c0001t0001g0238 a0001c0001t0001g0273 a0001c0003t0001g0220 |
3 | HG02602.hp1 HG02818.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.1538-518T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878773 | |||||||
| chr10:116878782 | G | A | 10 | a0001c0002t0001g0004 a0001c0002t0001g0023 a0001c0002t0001g0025 others(7): Show |
14 | HG00609.hp2 HG02083.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1538-509G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878782 | |||||||
| chr10:116878782 | G | C | 1 | a0001c0003t0001g0220 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1538-509G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878782 | |||||||
| chr10:116878787 | GA | G | 19 | a0001c0001t0002g0186 a0001c0001t0002g0190 a0001c0001t0003g0187 others(16): Show |
23 | HG00140.hp2 HG00609.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1538-503delA | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878787 | |||||||
| chr10:116878795 | G | A | 4 | a0001c0002t0003g0086 a0001c0002t0003g0087 a0001c0002t0003g0104 others(1): Show |
4 | HG01081.hp2 HG01261.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1538-496G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878795 | |||||||
| chr10:116878798 | C | T | 1 | a0001c0002t0003g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1538-493C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878798 | |||||||
| chr10:116878800 | G | A | 1 | a0001c0002t0003g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1538-491G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878800 | |||||||
| chr10:116878892 | T | C | 5 | a0001c0001t0001g0061 a0001c0001t0002g0042 a0001c0001t0004g0309 others(2): Show |
5 | HG01243.hp2 HG02273.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1538-399T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878892 | |||||||
| chr10:116878979 | A | G | 1 | a0001c0002t0002g0142 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1538-312A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878979 | |||||||
| chr10:116878986 | A | G | 1 | a0001c0002t0002g0142 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1538-305A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878986 | |||||||
| chr10:116878989 | T | C | 1 | a0001c0002t0002g0142 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1538-302T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878989 | |||||||
| chr10:116878994 | T | C | 1 | a0001c0002t0002g0142 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1538-297T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116878994 | |||||||
| chr10:116879022 | A | C | 2 | a0001c0001t0013g0307 a0001c0001t0013g0308 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1538-269A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116879022 | |||||||
| chr10:116879051 | T | A | 2 | a0001c0001t0008g0047 a0001c0001t0008g0048 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1538-240T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116879051 | |||||||
| chr10:116879055 | A | C | 1 | a0001c0002t0004g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1538-236A>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116879055 | |||||||
| chr10:116879077 | C | T | 1 | a0001c0002t0003g0107 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1538-214C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116879077 | |||||||
| chr10:116879109 | A | T | 19 | a0001c0002t0002g0088 a0001c0002t0004g0003 a0001c0002t0004g0039 others(16): Show |
22 | HG00423.hp2 HG01175.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1538-182A>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116879109 | |||||||
| chr10:116879241 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0002g0042 |
2 | HG01243.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1538-50G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116879241 | |||||||
| chr10:116879242 | T | G | 2 | a0001c0001t0001g0061 a0001c0001t0002g0042 |
2 | HG01243.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1538-49T>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 11/13 | chr10 | 116879242 | |||||||
| chr10:116879589 | C | G | 1 | a0001c0003t0006g0277 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1605+231C>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 12/13 | chr10 | 116879589 | |||||||
| chr10:116879631 | C | T | 325 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(322): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1606-238C>T | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 12/13 | chr10 | 116879631 | |||||||
| chr10:116879651 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0285 |
2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1606-218G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 12/13 | chr10 | 116879651 | |||||||
| chr10:116879839 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1606-30G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 12/13 | chr10 | 116879839 | |||||||
| chr10:116879856 | T | A | 2 | a0001c0001t0001g0061 a0001c0001t0002g0042 |
2 | HG01243.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1606-13T>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 12/13 | chr10 | 116879856 | |||||||
| chr10:116879856 | T | C | 1 | a0001c0001t0004g0309 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1606-13T>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 12/13 | chr10 | 116879856 | |||||||
| chr10:116880044 | G | C | 1 | a0001c0002t0003g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1723+58G>C | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 13/13 | chr10 | 116880044 | |||||||
| chr10:116880563 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1723+577G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 13/13 | chr10 | 116880563 | |||||||
| chr10:116880966 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0216 |
3 | HG02809.hp2 HG02965.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1724-549A>G | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 13/13 | chr10 | 116880966 | |||||||
| chr10:116881368 | G | A | 1 | a0001c0001t0005g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1724-147G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 13/13 | chr10 | 116881368 | |||||||
| chr10:116881388 | G | A | 1 | a0001c0002t0002g0157 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1724-127G>A | ENO4 | ENSG00000188316.16 | transcript | ENST00000341276.11 | protein_coding | 13/13 | chr10 | 116881388 |