Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9603 |
| ensemblid | ENSG00000050344.9 |
| hgncid | 7783 |
| symbol | NFE2L3 |
| name | NFE2 like bZIP transcription factor 3 |
| refseq_nuc | NM_004289.7 |
| refseq_prot | NP_004280.5 |
| ensembl_nuc | ENST00000056233.4 |
| ensembl_prot | ENSP00000056233.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 26152198 |
| end | 26187137 |
| strand | + |
| ver | v1.2 |
| region | chr7:26152198-26187137 |
| region5000 | chr7:26147198-26192137 |
| regionname0 | NFE2L3_chr7_26152198_26187137 |
| regionname5000 | NFE2L3_chr7_26147198_26192137 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 694 | 359 | 75 | 66 | 161 | 14 | 41 | 126 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0002 | 0/0 | 695 | 11 | 6 | 4 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(690): Show |
chr7 | 26147198 | 26192137 |
| a0003 | 0/0 | 694 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0004 | 0/0 | 694 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0005 | 0/0 | 694 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0006 | 0/0 | 694 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0007 | 0/0 | 694 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0008 | 0/0 | 694 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0009 | 0/0 | 694 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0010 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0011 | 0/0 | 694 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0012 | 0/0 | 694 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0013 | 0/0 | 694 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0014 | 0/0 | 694 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0015 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| a0016 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | MKHLK others(689): Show |
chr7 | 26147198 | 26192137 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2082 | 209 | 28 | 49 | 83 | 13 | 34 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0001c0002 | 0/0 | 2082 | 147 | 47 | 17 | 75 | 1 | 7 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0001c0005 | 0/0 | 2082 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0002c0004 | 0/0 | 2085 | 8 | 5 | 3 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2080): Show |
chr7 | 26147198 | 26192137 | ||
| a0002c0007 | 0/0 | 2085 | 3 | 1 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2080): Show |
chr7 | 26147198 | 26192137 | ||
| a0003c0003 | 0/0 | 2082 | 10 | 0 | 0 | 10 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0004c0006 | 0/0 | 2082 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0005c0010 | 0/0 | 2082 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0006c0009 | 0/0 | 2082 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0007c0012 | 0/0 | 2082 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0008c0011 | 0/0 | 2082 | 2 | 0 | 0 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0009c0008 | 0/0 | 2082 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0010c0016 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0011c0019 | 0/0 | 2082 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0012c0014 | 0/0 | 2082 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0013c0017 | 0/0 | 2082 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0014c0018 | 0/0 | 2082 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0015c0013 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 | ||
| a0016c0015 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | ATGAA others(2077): Show |
chr7 | 26147198 | 26192137 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3740 | 198 | 25 | 46 | 81 | 13 | 31 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0001t0005 | 0/0 | 3740 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0001t0013 | 0/0 | 3740 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0001t0018 | 0/0 | 3740 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0001t0019 | 0/0 | 3740 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0001t0020 | 0/0 | 3740 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0001t0021 | 0/0 | 3740 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0001t0022 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0001t0025 | 0/0 | 3740 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0001t0026 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0001 | 0/0 | 3740 | 29 | 27 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0002 | 0/0 | 3745 | 67 | 5 | 9 | 48 | 0 | 5 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3740): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0003 | 0/0 | 3738 | 11 | 0 | 4 | 7 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3733): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0004 | 0/0 | 3740 | 9 | 0 | 0 | 8 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0006 | 0/0 | 3740 | 7 | 6 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0007 | 0/0 | 3736 | 7 | 0 | 0 | 7 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3731): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0008 | 0/0 | 3740 | 5 | 2 | 1 | 0 | 1 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0010 | 0/0 | 3740 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0011 | 0/0 | 3735 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3730): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0014 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0015 | 0/0 | 3740 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0017 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3740): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0023 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0002t0024 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0001c0005t0001 | 0/0 | 3740 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0002c0004t0005 | 0/0 | 3743 | 6 | 3 | 3 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3738): Show |
chr7 | 26147198 | 26192137 |
| a0002c0004t0009 | 0/0 | 3743 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3738): Show |
chr7 | 26147198 | 26192137 |
| a0002c0007t0003 | 0/0 | 3741 | 3 | 1 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3736): Show |
chr7 | 26147198 | 26192137 |
| a0003c0003t0003 | 0/0 | 3738 | 9 | 0 | 0 | 9 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3733): Show |
chr7 | 26147198 | 26192137 |
| a0003c0003t0016 | 0/0 | 3738 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3733): Show |
chr7 | 26147198 | 26192137 |
| a0004c0006t0001 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0004c0006t0012 | 0/0 | 3740 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0005c0010t0002 | 0/0 | 3745 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3740): Show |
chr7 | 26147198 | 26192137 |
| a0006c0009t0003 | 0/0 | 3738 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3733): Show |
chr7 | 26147198 | 26192137 |
| a0007c0012t0009 | 0/0 | 3740 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0008c0011t0001 | 0/0 | 3740 | 2 | 0 | 0 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0009c0008t0001 | 0/0 | 3740 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0010c0016t0004 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0011c0019t0001 | 0/0 | 3740 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0012c0014t0001 | 0/0 | 3740 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0013c0017t0001 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0014c0018t0014 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0015c0013t0001 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3735): Show |
chr7 | 26147198 | 26192137 |
| a0016c0015t0003 | 0/0 | 3738 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | GGAGC others(3733): Show |
chr7 | 26147198 | 26192137 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 39 | 6 | 11 | 12 | 4 | 5 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0004 | 0/0 | 13 | 0 | 2 | 8 | 0 | 3 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0005 | 0/0 | 12 | 0 | 1 | 6 | 0 | 5 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0006 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0013g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0013g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0018g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0019g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0020g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0021g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0022g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0025g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0001t0026g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0009 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0002 | 0/0 | 20 | 0 | 7 | 13 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0008 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0003g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0004g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0006g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0007g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0007g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0008g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0008g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0008g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0010g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0010g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0011g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0015g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0015g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0023g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0002t0024g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0001c0005t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0002c0004t0005g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0002c0004t0005g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0002c0004t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0002c0004t0009g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0002c0007t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0002c0007t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0002c0007t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0003c0003t0003g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0003c0003t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0003c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0003c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0003c0003t0016g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0004c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0004c0006t0012g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0005c0010t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0006c0009t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0006c0009t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0007c0012t0009g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0008c0011t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0008c0011t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0009c0008t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0009c0008t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0010c0016t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0011c0019t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0012c0014t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0013c0017t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0014c0018t0014g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0015c0013t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| a0016c0015t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00423 | hp2 | a0001 | c0002 | t0007 | g0003 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00438 | hp1 | a0010 | c0016 | t0004 | g0003 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00544 | hp2 | a0005 | c0010 | t0002 | g0038 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00609 | hp1 | a0001 | c0002 | t0004 | g0079 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00642 | hp1 | a0001 | c0001 | t0019 | g0127 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0206 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0013 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG00741 | hp2 | a0002 | c0004 | t0005 | g0041 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01081 | hp2 | a0001 | c0001 | t0013 | g0067 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01099 | hp2 | a0001 | c0002 | t0008 | g0024 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0013 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01106 | hp2 | a0002 | c0007 | t0003 | g0198 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01109 | hp1 | a0001 | c0002 | t0006 | g0061 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01167 | hp2 | a0002 | c0004 | t0005 | g0022 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01169 | hp2 | a0002 | c0004 | t0005 | g0041 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01358 | hp1 | a0001 | c0001 | t0021 | g0006 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01361 | hp1 | a0011 | c0019 | t0001 | g0225 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0165 | AMR | CLM | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01517 | hp2 | a0001 | c0002 | t0008 | g0054 | EUR | IBS | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0013 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02015 | hp2 | a0001 | c0001 | t0026 | g0080 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0222 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02027 | hp2 | a0006 | c0009 | t0003 | g0197 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02055 | hp1 | a0001 | c0002 | t0006 | g0134 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02055 | hp2 | a0002 | c0004 | t0005 | g0022 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02129 | hp1 | a0001 | c0002 | t0007 | g0029 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02145 | hp2 | a0007 | c0012 | t0009 | g0001 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02165 | hp2 | a0001 | c0002 | t0007 | g0003 | EAS | CDX | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02258 | hp1 | a0004 | c0006 | t0012 | g0023 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02258 | hp2 | a0001 | c0002 | t0006 | g0059 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02273 | hp1 | a0012 | c0014 | t0001 | g0001 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02280 | hp2 | a0013 | c0017 | t0001 | g0073 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02451 | hp1 | a0001 | c0002 | t0011 | g0019 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02451 | hp2 | a0001 | c0002 | t0008 | g0056 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02572 | hp2 | a0002 | c0004 | t0005 | g0221 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02647 | hp1 | a0002 | c0004 | t0009 | g0036 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02683 | hp1 | a0001 | c0002 | t0004 | g0106 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02683 | hp2 | a0008 | c0011 | t0001 | g0098 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02735 | hp1 | a0002 | c0007 | t0003 | g0196 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0141 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02895 | hp2 | a0001 | c0002 | t0006 | g0060 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02922 | hp2 | a0001 | c0002 | t0011 | g0019 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02970 | hp2 | a0002 | c0004 | t0009 | g0036 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03017 | hp1 | a0001 | c0002 | t0008 | g0055 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03041 | hp1 | a0001 | c0002 | t0024 | g0043 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03139 | hp2 | a0001 | c0002 | t0011 | g0019 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03195 | hp1 | a0007 | c0012 | t0009 | g0001 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03195 | hp2 | a0014 | c0018 | t0014 | g0120 | AFR | ESN | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03209 | hp2 | a0001 | c0002 | t0014 | g0066 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03225 | hp2 | a0002 | c0004 | t0005 | g0022 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03486 | hp1 | a0002 | c0007 | t0003 | g0191 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03491 | hp2 | a0001 | c0001 | t0020 | g0006 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0186 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03579 | hp2 | a0001 | c0002 | t0006 | g0016 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0040 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0218 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03942 | hp1 | a0008 | c0011 | t0001 | g0099 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03942 | hp2 | a0001 | c0001 | t0018 | g0192 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18522 | hp2 | a0001 | c0002 | t0006 | g0016 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18612 | hp1 | a0001 | c0002 | t0004 | g0149 | EAS | CHB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | CHB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | CHB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | CHB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18940 | hp1 | a0001 | c0002 | t0010 | g0116 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18947 | hp2 | a0001 | c0002 | t0010 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18950 | hp2 | a0001 | c0002 | t0007 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0150 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18959 | hp1 | a0015 | c0013 | t0001 | g0094 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18959 | hp2 | a0005 | c0010 | t0002 | g0038 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18967 | hp1 | a0001 | c0002 | t0017 | g0039 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0203 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18971 | hp1 | a0003 | c0003 | t0016 | g0007 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18971 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18973 | hp1 | a0001 | c0002 | t0007 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18974 | hp1 | a0001 | c0002 | t0007 | g0029 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18974 | hp2 | a0003 | c0003 | t0003 | g0193 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18975 | hp2 | a0001 | c0001 | t0022 | g0006 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18982 | hp1 | a0001 | c0005 | t0001 | g0183 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18983 | hp2 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18990 | hp1 | a0009 | c0008 | t0001 | g0171 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18997 | hp2 | a0003 | c0003 | t0003 | g0190 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18999 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA18999 | hp2 | a0001 | c0002 | t0023 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19002 | hp2 | a0003 | c0003 | t0003 | g0037 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19004 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19009 | hp2 | a0009 | c0008 | t0001 | g0169 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19012 | hp1 | a0016 | c0015 | t0003 | g0195 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19043 | hp2 | a0001 | c0002 | t0015 | g0226 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19057 | hp1 | a0003 | c0003 | t0003 | g0037 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19065 | hp2 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19067 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19068 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19078 | hp2 | a0001 | c0002 | t0010 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19079 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19079 | hp2 | a0001 | c0002 | t0007 | g0194 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19083 | hp1 | a0006 | c0009 | t0003 | g0007 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19085 | hp2 | a0001 | c0005 | t0001 | g0156 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19086 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19240 | hp1 | a0001 | c0002 | t0008 | g0024 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ASW | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | ASW | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA20905 | hp1 | a0001 | c0001 | t0025 | g0006 | SAS | GIH | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02486 | hp2 | a0001 | c0002 | t0015 | g0087 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG02559 | hp2 | a0004 | c0006 | t0012 | g0023 | AFR | ACB | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG06807 | hp1 | a0001 | c0002 | t0006 | g0016 | AFR | USA | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | USA | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | USA | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA21309 | hp1 | a0004 | c0006 | t0001 | g0045 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | LWK | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0140 | REF | REF | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | NFE2L3_chr7_26147198_26192137 | NFE2L3 | chr7 | 26147198 | 26192137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:26152564 | C | G | 1 | a0011 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.66C>G | p.Ser22Arg | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 367/3740 | 66/2085 | 22/694 | chr7 | 26152564 | |||
| chr7:26152597 | C | CCTG | 1 | a0002 | 11 | HG00741.hp2 HG01106.hp2 HG01167.hp2 others(8): Show |
disruptive_inframe_insertion | MODERATE | c.107_109dupTGC | p.Leu36dup | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 411/3740 | 110/2085 | 37/694 | INFO_REALIGN_3_PRIME | chr7 | 26152597 | ||
| chr7:26152772 | C | T | 1 | a0007 | 2 | HG02145.hp2 HG03195.hp1 |
missense_variant | MODERATE | c.274C>T | p.Leu92Phe | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 575/3740 | 274/2085 | 92/694 | chr7 | 26152772 | |||
| chr7:26152980 | G | A | 1 | a0015 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.482G>A | p.Arg161Gln | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 783/3740 | 482/2085 | 161/694 | chr7 | 26152980 | |||
| chr7:26153047 | C | G | 1 | a0008 | 2 | HG02683.hp2 HG03942.hp1 |
missense_variant | MODERATE | c.549C>G | p.Asp183Glu | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 850/3740 | 549/2085 | 183/694 | chr7 | 26153047 | |||
| chr7:26178049 | A | G | 1 | a0014 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.677A>G | p.Asn226Ser | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/4 | 978/3740 | 677/2085 | 226/694 | chr7 | 26178049 | |||
| chr7:26178061 | A | G | 1 | a0004 | 3 | HG02258.hp1 HG02559.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.689A>G | p.Glu230Gly | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/4 | 990/3740 | 689/2085 | 230/694 | chr7 | 26178061 | |||
| chr7:26184623 | A | G | 1 | a0013 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.925A>G | p.Ile309Val | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1226/3740 | 925/2085 | 309/694 | chr7 | 26184623 | |||
| chr7:26184819 | A | G | 1 | a0005 | 2 | HG00544.hp2 NA18959.hp2 |
missense_variant | MODERATE | c.1121A>G | p.Asn374Ser | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1422/3740 | 1121/2085 | 374/694 | chr7 | 26184819 | |||
| chr7:26185020 | T | A | 1 | a0009 | 2 | NA18990.hp1 NA19009.hp2 |
missense_variant | MODERATE | c.1322T>A | p.Val441Glu | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1623/3740 | 1322/2085 | 441/694 | chr7 | 26185020 | |||
| chr7:26185116 | G | A | 1 | a0016 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.1418G>A | p.Ser473Asn | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1719/3740 | 1418/2085 | 473/694 | chr7 | 26185116 | |||
| chr7:26185161 | A | G | 1 | a0012 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.1463A>G | p.Asp488Gly | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1764/3740 | 1463/2085 | 488/694 | chr7 | 26185161 | |||
| chr7:26185402 | A | C | 1 | a0010 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1704A>C | p.Arg568Ser | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 2005/3740 | 1704/2085 | 568/694 | chr7 | 26185402 | |||
| chr7:26185548 | A | C | 2 | a0006 a0016 |
3 | HG02027.hp2 NA19012.hp1 NA19083.hp1 |
missense_variant | MODERATE | c.1850A>C | p.Lys617Thr | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 2151/3740 | 1850/2085 | 617/694 | chr7 | 26185548 | |||
| chr7:26185559 | A | G | 1 | a0003 | 10 | NA18971.hp1 NA18974.hp2 NA18983.hp2 others(7): Show |
missense_variant | MODERATE | c.1861A>G | p.Lys621Glu | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 2162/3740 | 1861/2085 | 621/694 | chr7 | 26185559 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:26185048 | C | T | 9 | a0001c0002 a0002c0007 a0003c0003 others(6): Show |
168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
synonymous_variant | LOW | c.1350C>T | p.Cys450Cys | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1651/3740 | 1350/2085 | 450/694 | chr7 | 26185048 | |||
| chr7:26185519 | A | G | 1 | a0001c0005 | 3 | NA18982.hp1 NA19079.hp1 NA19085.hp2 |
synonymous_variant | LOW | c.1821A>G | p.Glu607Glu | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 2122/3740 | 1821/2085 | 607/694 | chr7 | 26185519 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:26152240 | G | C | 1 | a0003c0003t0016 | 1 | NA18971.hp1 | 5_prime_UTR_variant | MODIFIER | c.-259G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 259 | chr7 | 26152240 | ||||||
| chr7:26152419 | G | A | 1 | a0001c0002t0017 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/4 | 80 | chr7 | 26152419 | ||||||
| chr7:26185800 | G | T | 1 | a0001c0002t0015 | 2 | HG02486.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*17G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 17 | chr7 | 26185800 | ||||||
| chr7:26185836 | A | G | 1 | a0001c0001t0026 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 53 | chr7 | 26185836 | ||||||
| chr7:26185913 | C | A | 1 | a0001c0002t0006 | 7 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*130C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 130 | chr7 | 26185913 | ||||||
| chr7:26186029 | T | C | 1 | a0001c0001t0018 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 246 | chr7 | 26186029 | ||||||
| chr7:26186149 | G | A | 1 | a0001c0002t0010 | 3 | NA18940.hp1 NA18947.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*366G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 366 | chr7 | 26186149 | ||||||
| chr7:26186152 | T | A | 2 | a0002c0004t0009 a0007c0012t0009 |
4 | HG02145.hp2 HG02647.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*369T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 369 | chr7 | 26186152 | ||||||
| chr7:26186244 | CTT | C | 7 | a0001c0002t0003 a0001c0002t0011 a0002c0007t0003 others(4): Show |
30 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*462_*463delTT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 462 | chr7 | 26186244 | ||||||
| chr7:26186265 | G | A | 1 | a0004c0006t0012 | 2 | HG02258.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*482G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 482 | chr7 | 26186265 | ||||||
| chr7:26186298 | C | T | 1 | a0001c0001t0025 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*515C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 515 | chr7 | 26186298 | ||||||
| chr7:26186333 | CCTTA | C | 1 | a0001c0002t0007 | 7 | HG00423.hp2 HG02129.hp1 HG02165.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*554_*557delACTT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 554 | INFO_REALIGN_3_PRIME | chr7 | 26186333 | |||||
| chr7:26186402 | C | T | 2 | a0001c0001t0005 a0002c0004t0005 |
8 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*619C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 619 | chr7 | 26186402 | ||||||
| chr7:26186479 | A | ATACTT | 3 | a0001c0002t0002 a0001c0002t0017 a0005c0010t0002 |
70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*697_*701dupTACTT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 702 | INFO_REALIGN_3_PRIME | chr7 | 26186479 | |||||
| chr7:26186517 | C | T | 1 | a0001c0002t0008 | 5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*734C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 734 | chr7 | 26186517 | ||||||
| chr7:26186569 | C | T | 6 | a0001c0002t0003 a0002c0007t0003 a0003c0003t0003 others(3): Show |
27 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*786C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 786 | chr7 | 26186569 | ||||||
| chr7:26186723 | G | T | 1 | a0001c0002t0024 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 940 | chr7 | 26186723 | ||||||
| chr7:26186808 | C | A | 1 | a0001c0001t0019 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1025C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1025 | chr7 | 26186808 | ||||||
| chr7:26186808 | C | T | 5 | a0001c0002t0004 a0001c0002t0007 a0001c0002t0010 others(2): Show |
21 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1025C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1025 | chr7 | 26186808 | ||||||
| chr7:26186830 | A | G | 1 | a0001c0001t0022 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1047A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1047 | chr7 | 26186830 | ||||||
| chr7:26186834 | T | G | 1 | a0001c0001t0013 | 2 | HG01081.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1051T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1051 | chr7 | 26186834 | ||||||
| chr7:26186959 | G | A | 1 | a0001c0002t0023 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1176G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1176 | chr7 | 26186959 | ||||||
| chr7:26187009 | ATAT | A | 1 | a0001c0002t0011 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1231_*1233delATT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1231 | INFO_REALIGN_3_PRIME | chr7 | 26187009 | |||||
| chr7:26187034 | A | G | 2 | a0001c0002t0014 a0014c0018t0014 |
2 | HG03195.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1251A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1251 | chr7 | 26187034 | ||||||
| chr7:26187086 | A | G | 1 | a0001c0001t0021 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1303A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1303 | chr7 | 26187086 | ||||||
| chr7:26187126 | T | G | 1 | a0001c0001t0020 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1343T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 4/4 | 1343 | chr7 | 26187126 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:26153193 | G | A | 4 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+125G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153193 | |||||||
| chr7:26153216 | C | G | 1 | a0001c0002t0015g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+148C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153216 | |||||||
| chr7:26153312 | C | T | 1 | a0011c0019t0001g0225 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.570+244C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153312 | |||||||
| chr7:26153536 | A | G | 1 | a0001c0002t0015g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+468A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153536 | |||||||
| chr7:26153539 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.570+471G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153539 | |||||||
| chr7:26153540 | C | A | 1 | a0001c0001t0001g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.570+472C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153540 | |||||||
| chr7:26153556 | C | T | 61 | a0001c0001t0001g0184 a0001c0001t0001g0187 a0001c0001t0001g0201 others(58): Show |
113 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.570+488C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153556 | |||||||
| chr7:26153618 | C | T | 1 | a0001c0002t0002g0223 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.570+550C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153618 | |||||||
| chr7:26153689 | C | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(164): Show |
264 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.570+621C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153689 | |||||||
| chr7:26153740 | T | G | 1 | a0001c0005t0001g0183 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.570+672T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153740 | |||||||
| chr7:26153838 | A | G | 1 | a0001c0002t0001g0044 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.570+770A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153838 | |||||||
| chr7:26153853 | C | T | 1 | a0001c0002t0003g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.570+785C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153853 | |||||||
| chr7:26153886 | C | T | 1 | a0001c0002t0002g0223 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.570+818C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153886 | |||||||
| chr7:26153898 | T | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG03669.hp2 HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.570+830T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153898 | |||||||
| chr7:26153899 | C | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG03669.hp2 HG03710.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.570+831C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26153899 | |||||||
| chr7:26154017 | T | C | 1 | a0004c0006t0012g0023 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.570+949T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154017 | |||||||
| chr7:26154114 | A | AG | 3 | a0001c0002t0001g0046 a0004c0006t0001g0045 a0004c0006t0012g0023 |
4 | HG02258.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1050dupG | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26154114 | ||||||
| chr7:26154153 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.570+1085T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154153 | |||||||
| chr7:26154185 | C | T | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.570+1117C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154185 | |||||||
| chr7:26154535 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
7 | HG00642.hp1 HG01192.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+1467T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154535 | |||||||
| chr7:26154582 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.570+1514G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154582 | |||||||
| chr7:26154590 | G | A | 1 | a0001c0002t0002g0185 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.570+1522G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154590 | |||||||
| chr7:26154644 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.570+1576C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154644 | |||||||
| chr7:26154657 | C | G | 3 | a0002c0004t0005g0022 a0002c0004t0005g0041 a0002c0004t0005g0221 |
6 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+1589C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154657 | |||||||
| chr7:26154928 | A | C | 1 | a0001c0002t0002g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.570+1860A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154928 | |||||||
| chr7:26154933 | G | A | 1 | a0001c0002t0002g0186 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.570+1865G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26154933 | |||||||
| chr7:26155240 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.570+2172C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155240 | |||||||
| chr7:26155319 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.570+2251G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155319 | |||||||
| chr7:26155373 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0181 |
3 | NA18944.hp2 NA18950.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.570+2305C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155373 | |||||||
| chr7:26155396 | T | A | 1 | a0001c0002t0002g0047 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.570+2328T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155396 | |||||||
| chr7:26155438 | T | A | 1 | a0001c0002t0003g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.570+2370T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155438 | |||||||
| chr7:26155564 | CATTA | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG00738.hp2 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+2502_570+2505d others(6): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26155564 | ||||||
| chr7:26155974 | C | T | 122 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(119): Show |
197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.570+2906C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26155974 | |||||||
| chr7:26156058 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
5 | HG00733.hp2 HG01175.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+2990G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156058 | |||||||
| chr7:26156199 | G | T | 1 | a0001c0002t0001g0064 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.570+3131G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156199 | |||||||
| chr7:26156209 | A | C | 2 | a0001c0002t0001g0117 a0001c0002t0001g0118 |
2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.570+3141A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156209 | |||||||
| chr7:26156239 | C | T | 1 | a0002c0007t0003g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.570+3171C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156239 | |||||||
| chr7:26156520 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.570+3452T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156520 | |||||||
| chr7:26156810 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.570+3742C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156810 | |||||||
| chr7:26156835 | G | A | 1 | a0001c0002t0014g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+3767G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156835 | |||||||
| chr7:26156969 | G | A | 1 | a0001c0002t0002g0199 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.570+3901G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26156969 | |||||||
| chr7:26157044 | G | A | 1 | a0001c0002t0002g0200 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.570+3976G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157044 | |||||||
| chr7:26157064 | A | C | 1 | a0001c0002t0010g0116 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.570+3996A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157064 | |||||||
| chr7:26157077 | A | G | 4 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+4009A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157077 | |||||||
| chr7:26157199 | G | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(161): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.570+4131G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157199 | |||||||
| chr7:26157282 | A | G | 17 | a0001c0001t0001g0065 a0001c0002t0001g0009 a0001c0002t0001g0042 others(14): Show |
24 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.570+4214A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157282 | |||||||
| chr7:26157343 | G | A | 159 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(156): Show |
255 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.570+4275G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157343 | |||||||
| chr7:26157345 | T | A | 1 | a0001c0002t0002g0047 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.570+4277T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157345 | |||||||
| chr7:26157418 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.570+4350C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157418 | |||||||
| chr7:26157524 | A | G | 1 | a0001c0002t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570+4456A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157524 | |||||||
| chr7:26157779 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.570+4711T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26157779 | |||||||
| chr7:26158059 | T | G | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(118): Show |
197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.570+4991T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158059 | |||||||
| chr7:26158060 | TA | T | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(118): Show |
197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.570+4993delA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158060 | |||||||
| chr7:26158206 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0135 a0001c0001t0001g0136 others(6): Show |
15 | HG00741.hp2 HG01081.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.570+5138G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158206 | |||||||
| chr7:26158420 | T | C | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(81): Show |
121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.570+5352T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158420 | |||||||
| chr7:26158518 | C | T | 2 | a0001c0002t0001g0112 a0001c0002t0001g0133 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.570+5450C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158518 | |||||||
| chr7:26158587 | A | G | 163 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(160): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.570+5519A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158587 | |||||||
| chr7:26158883 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.570+5815A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26158883 | |||||||
| chr7:26159043 | G | C | 1 | a0001c0002t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.570+5975G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159043 | |||||||
| chr7:26159065 | C | T | 1 | a0001c0002t0002g0219 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.570+5997C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159065 | |||||||
| chr7:26159105 | A | G | 11 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.570+6037A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159105 | |||||||
| chr7:26159490 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.570+6422A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159490 | |||||||
| chr7:26159587 | A | G | 162 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(159): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.570+6519A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159587 | |||||||
| chr7:26159900 | G | A | 19 | a0001c0001t0018g0192 a0001c0002t0003g0007 a0001c0002t0003g0013 others(16): Show |
29 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.570+6832G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26159900 | |||||||
| chr7:26159949 | C | CT | 38 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0063 others(35): Show |
50 | HG00544.hp1 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.570+6901dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26159949 | ||||||
| chr7:26159949 | C | CTT | 11 | a0001c0001t0001g0051 a0001c0001t0001g0062 a0001c0001t0001g0065 others(8): Show |
12 | HG00639.hp1 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.570+6900_570+6901d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26159949 | ||||||
| chr7:26160247 | G | A | 1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570+7179G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160247 | |||||||
| chr7:26160493 | C | G | 1 | a0001c0002t0007g0029 | 2 | HG02129.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.570+7425C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160493 | |||||||
| chr7:26160593 | A | G | 164 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(161): Show |
260 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.570+7525A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160593 | |||||||
| chr7:26160595 | T | C | 38 | a0001c0001t0001g0184 a0001c0001t0001g0201 a0001c0002t0001g0112 others(35): Show |
75 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(72): Show |
intron_variant | MODIFIER | c.570+7527T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160595 | |||||||
| chr7:26160735 | A | G | 4 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0110 others(1): Show |
4 | NA18946.hp1 NA18960.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+7667A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160735 | |||||||
| chr7:26160797 | C | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(79): Show |
119 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.570+7729C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160797 | |||||||
| chr7:26160836 | A | G | 1 | a0001c0001t0001g0011 | 4 | NA18957.hp1 NA18977.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+7768A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26160836 | |||||||
| chr7:26161333 | CTCT | C | 3 | a0001c0002t0002g0015 a0001c0002t0002g0202 a0001c0002t0002g0215 |
6 | NA18747.hp2 NA18947.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+8267_570+8269d others(5): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26161333 | ||||||
| chr7:26161335 | CT | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(52): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.570+8296delT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26161335 | ||||||
| chr7:26161335 | CTT | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0144 others(4): Show |
11 | HG02132.hp1 HG02273.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+8295_570+8296d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26161335 | ||||||
| chr7:26161337 | T | C | 5 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0110 others(2): Show |
5 | HG01081.hp2 NA18946.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+8269T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161337 | |||||||
| chr7:26161339 | T | C | 1 | a0001c0002t0002g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.570+8271T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161339 | |||||||
| chr7:26161348 | TTTTTTTT others(10): Show |
T | 1 | a0001c0002t0015g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+8281_570+8297d others(19): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161348 | |||||||
| chr7:26161350 | TTTTTTTT others(8): Show |
T | 2 | a0001c0002t0001g0076 a0001c0002t0002g0008 |
2 | HG03041.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.570+8283_570+8297d others(17): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161350 | |||||||
| chr7:26161352 | TTTTTTTT others(6): Show |
T | 1 | a0001c0001t0001g0011 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.570+8285_570+8297d others(15): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161352 | |||||||
| chr7:26161353 | TTTTTTTT others(5): Show |
T | 2 | a0001c0001t0001g0204 a0001c0002t0001g0112 |
2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.570+8286_570+8297d others(14): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161353 | |||||||
| chr7:26161354 | TTTTTTTT others(4): Show |
T | 1 | a0001c0002t0014g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+8287_570+8297d others(13): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161354 | |||||||
| chr7:26161355 | TTTTTTTT others(3): Show |
T | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.570+8288_570+8297d others(12): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161355 | |||||||
| chr7:26161360 | TTTTTG | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0101 a0001c0001t0001g0102 others(23): Show |
35 | HG00741.hp2 HG01071.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.570+8293_570+8297d others(7): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161360 | |||||||
| chr7:26161361 | TTTTG | T | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(81): Show |
120 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.570+8294_570+8297d others(6): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161361 | |||||||
| chr7:26161362 | TTTG | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0052 others(12): Show |
19 | HG00438.hp1 HG00741.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.570+8295_570+8297d others(5): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161362 | |||||||
| chr7:26161363 | TTG | T | 28 | a0001c0001t0001g0184 a0001c0001t0001g0201 a0001c0002t0001g0210 others(25): Show |
57 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.570+8296_570+8297d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161363 | |||||||
| chr7:26161364 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.570+8296T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161364 | |||||||
| chr7:26161364 | TG | T | 7 | a0001c0002t0002g0002 a0001c0002t0002g0014 a0001c0002t0002g0020 others(4): Show |
7 | HG02071.hp2 NA18964.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+8299delG | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26161364 | ||||||
| chr7:26161365 | G | T | 5 | a0001c0002t0002g0015 a0001c0002t0002g0047 a0001c0002t0002g0202 others(2): Show |
10 | HG02451.hp1 HG02922.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+8297G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161365 | |||||||
| chr7:26161412 | A | G | 1 | a0003c0003t0003g0037 | 2 | NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.570+8344A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161412 | |||||||
| chr7:26161486 | G | A | 3 | a0002c0004t0005g0022 a0002c0004t0005g0041 a0002c0004t0005g0221 |
6 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+8418G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161486 | |||||||
| chr7:26161572 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0100 |
4 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+8504C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161572 | |||||||
| chr7:26161590 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.570+8522C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161590 | |||||||
| chr7:26161778 | G | A | 1 | a0002c0004t0009g0036 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.570+8710G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26161778 | |||||||
| chr7:26162051 | G | A | 1 | a0001c0001t0013g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.570+8983G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162051 | |||||||
| chr7:26162142 | C | CA | 28 | a0001c0001t0001g0051 a0001c0001t0001g0065 a0001c0001t0001g0068 others(25): Show |
35 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.570+9091dupA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26162142 | ||||||
| chr7:26162202 | A | G | 2 | a0008c0011t0001g0098 a0008c0011t0001g0099 |
2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.570+9134A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162202 | |||||||
| chr7:26162309 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.570+9241G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162309 | |||||||
| chr7:26162470 | GAA | G | 1 | a0001c0001t0001g0018 | 3 | HG00639.hp2 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.570+9404_570+9405d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26162470 | ||||||
| chr7:26162693 | T | C | 3 | a0001c0001t0005g0070 a0001c0001t0005g0104 a0011c0019t0001g0225 |
3 | HG01361.hp1 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.570+9625T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162693 | |||||||
| chr7:26162788 | C | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(114): Show |
173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.570+9720C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162788 | |||||||
| chr7:26162870 | G | A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(154): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.570+9802G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26162870 | |||||||
| chr7:26163197 | A | G | 1 | a0001c0002t0006g0060 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.570+10129A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163197 | |||||||
| chr7:26163251 | C | T | 1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570+10183C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163251 | |||||||
| chr7:26163375 | T | C | 1 | a0001c0001t0013g0141 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.570+10307T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163375 | |||||||
| chr7:26163391 | G | A | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.570+10323G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163391 | |||||||
| chr7:26163590 | G | T | 2 | a0001c0001t0005g0070 a0001c0001t0005g0104 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.570+10522G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163590 | |||||||
| chr7:26163619 | T | A | 1 | a0005c0010t0002g0038 | 2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.570+10551T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163619 | |||||||
| chr7:26163621 | A | C | 1 | a0005c0010t0002g0038 | 2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.570+10553A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163621 | |||||||
| chr7:26163815 | C | T | 2 | a0001c0001t0005g0070 a0001c0001t0005g0104 |
2 | HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.570+10747C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163815 | |||||||
| chr7:26163911 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0105 |
2 | NA18962.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.570+10843G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163911 | |||||||
| chr7:26163971 | G | A | 37 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(34): Show |
74 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(71): Show |
intron_variant | MODIFIER | c.570+10903G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163971 | |||||||
| chr7:26163982 | A | G | 37 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(34): Show |
74 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(71): Show |
intron_variant | MODIFIER | c.570+10914A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26163982 | |||||||
| chr7:26164364 | T | C | 4 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+11296T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26164364 | |||||||
| chr7:26164387 | C | T | 1 | a0006c0009t0003g0197 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.570+11319C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26164387 | |||||||
| chr7:26164884 | A | G | 1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570+11816A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26164884 | |||||||
| chr7:26165031 | A | G | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.570+11963A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165031 | |||||||
| chr7:26165052 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.570+11984C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165052 | |||||||
| chr7:26165057 | T | C | 1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.570+11989T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165057 | |||||||
| chr7:26165187 | C | A | 1 | a0001c0002t0004g0106 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.570+12119C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165187 | |||||||
| chr7:26165224 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.570+12156A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165224 | |||||||
| chr7:26165257 | G | A | 1 | a0002c0007t0003g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.570+12189G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165257 | |||||||
| chr7:26165323 | G | A | 1 | a0001c0002t0014g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+12255G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165323 | |||||||
| chr7:26165419 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.570+12351T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165419 | |||||||
| chr7:26165708 | G | A | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-12235G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165708 | |||||||
| chr7:26165816 | C | T | 1 | a0002c0007t0003g0196 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-12127C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165816 | |||||||
| chr7:26165900 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0097 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.571-12043A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165900 | |||||||
| chr7:26165982 | C | T | 1 | a0001c0002t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.571-11961C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26165982 | |||||||
| chr7:26166029 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.571-11914A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166029 | |||||||
| chr7:26166136 | CG | C | 157 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(154): Show |
251 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.571-11800delG | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26166136 | ||||||
| chr7:26166230 | G | C | 11 | a0001c0002t0001g0017 a0001c0002t0001g0025 a0001c0002t0001g0074 others(8): Show |
14 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.571-11713G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166230 | |||||||
| chr7:26166249 | G | A | 1 | a0001c0001t0001g0011 | 4 | NA18957.hp1 NA18977.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-11694G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166249 | |||||||
| chr7:26166360 | C | T | 34 | a0001c0001t0001g0184 a0001c0002t0001g0210 a0001c0002t0002g0002 others(31): Show |
71 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(68): Show |
intron_variant | MODIFIER | c.571-11583C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166360 | |||||||
| chr7:26166400 | G | A | 1 | a0001c0002t0008g0054 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.571-11543G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166400 | |||||||
| chr7:26166589 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.571-11354T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166589 | |||||||
| chr7:26166678 | A | C | 1 | a0016c0015t0003g0195 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.571-11265A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166678 | |||||||
| chr7:26166854 | C | T | 1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-11089C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26166854 | |||||||
| chr7:26167033 | G | A | 1 | a0008c0011t0001g0098 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.571-10910G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167033 | |||||||
| chr7:26167058 | T | C | 4 | a0001c0002t0002g0020 a0001c0002t0002g0047 a0001c0002t0002g0111 others(1): Show |
6 | NA18949.hp2 NA18952.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-10885T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167058 | |||||||
| chr7:26167101 | C | A | 2 | a0001c0002t0003g0188 a0001c0002t0003g0189 |
2 | HG00438.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.571-10842C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167101 | |||||||
| chr7:26167175 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | NA18981.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.571-10768G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167175 | |||||||
| chr7:26167494 | A | T | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-10449A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167494 | |||||||
| chr7:26167529 | C | CT | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-10403dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26167529 | ||||||
| chr7:26167736 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.571-10207C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167736 | |||||||
| chr7:26167864 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.571-10079C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167864 | |||||||
| chr7:26167970 | G | A | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9973G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26167970 | |||||||
| chr7:26168103 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0052 others(12): Show |
28 | HG00609.hp2 HG00642.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.571-9840C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168103 | |||||||
| chr7:26168135 | C | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(116): Show |
175 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.571-9808C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168135 | |||||||
| chr7:26168163 | G | T | 1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-9780G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168163 | |||||||
| chr7:26168405 | A | G | 156 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(153): Show |
248 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.571-9538A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168405 | |||||||
| chr7:26168426 | G | GTGCCCAG others(113): Show |
156 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(153): Show |
249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.571-9516_571-9515i others(122): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26168426 | ||||||
| chr7:26168470 | G | A | 1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-9473G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168470 | |||||||
| chr7:26168516 | G | T | 18 | a0001c0001t0018g0192 a0001c0002t0003g0007 a0001c0002t0003g0013 others(15): Show |
27 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.571-9427G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168516 | |||||||
| chr7:26168517 | A | G | 18 | a0001c0001t0018g0192 a0001c0002t0003g0007 a0001c0002t0003g0013 others(15): Show |
27 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.571-9426A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168517 | |||||||
| chr7:26168524 | G | A | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9419G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168524 | |||||||
| chr7:26168530 | AAT | A | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9403_571-9402d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26168530 | ||||||
| chr7:26168567 | T | G | 3 | a0002c0004t0005g0022 a0002c0004t0005g0041 a0002c0004t0005g0221 |
6 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-9376T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168567 | |||||||
| chr7:26168569 | G | T | 37 | a0001c0001t0001g0184 a0001c0002t0001g0046 a0001c0002t0001g0112 others(34): Show |
74 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(71): Show |
intron_variant | MODIFIER | c.571-9374G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168569 | |||||||
| chr7:26168772 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.571-9171C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168772 | |||||||
| chr7:26168796 | G | A | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9147G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168796 | |||||||
| chr7:26168868 | A | G | 36 | a0001c0001t0001g0184 a0001c0002t0001g0112 a0001c0002t0001g0133 others(33): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-9075A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26168868 | |||||||
| chr7:26169116 | G | A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(154): Show |
250 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.571-8827G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169116 | |||||||
| chr7:26169128 | T | C | 2 | a0001c0002t0006g0016 a0001c0002t0006g0061 |
4 | HG01109.hp1 HG03579.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-8815T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169128 | |||||||
| chr7:26169185 | C | T | 157 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(154): Show |
250 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.571-8758C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169185 | |||||||
| chr7:26169369 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.571-8574A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169369 | |||||||
| chr7:26169374 | C | T | 2 | a0001c0002t0007g0194 a0016c0015t0003g0195 |
2 | NA19012.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.571-8569C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169374 | |||||||
| chr7:26169441 | G | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(116): Show |
174 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.571-8502G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169441 | |||||||
| chr7:26169497 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.571-8446G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169497 | |||||||
| chr7:26169586 | C | A | 156 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(153): Show |
248 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(245): Show |
intron_variant | MODIFIER | c.571-8357C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169586 | |||||||
| chr7:26169811 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0167 |
7 | HG00597.hp1 NA18946.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-8132A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169811 | |||||||
| chr7:26169835 | C | T | 37 | a0001c0001t0001g0184 a0001c0002t0001g0046 a0001c0002t0001g0112 others(34): Show |
74 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(71): Show |
intron_variant | MODIFIER | c.571-8108C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26169835 | |||||||
| chr7:26169935 | CA | C | 34 | a0001c0001t0001g0184 a0001c0002t0001g0210 a0001c0002t0002g0002 others(31): Show |
73 | HG00544.hp2 HG00733.hp1 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.571-7997delA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26169935 | ||||||
| chr7:26170126 | A | G | 12 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(9): Show |
18 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-7817A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26170126 | |||||||
| chr7:26170686 | C | A | 67 | a0001c0001t0001g0179 a0001c0001t0001g0204 a0001c0001t0018g0192 others(64): Show |
100 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.571-7257C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26170686 | |||||||
| chr7:26170908 | C | T | 1 | a0001c0002t0006g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.571-7035C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26170908 | |||||||
| chr7:26170926 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.571-7017G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26170926 | |||||||
| chr7:26171030 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.571-6913A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171030 | |||||||
| chr7:26171089 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.571-6854A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171089 | |||||||
| chr7:26171140 | C | G | 9 | a0001c0002t0001g0017 a0001c0002t0001g0025 a0001c0002t0001g0074 others(6): Show |
12 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-6803C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171140 | |||||||
| chr7:26171183 | A | G | 31 | a0001c0001t0001g0179 a0001c0001t0026g0080 a0001c0002t0001g0017 others(28): Show |
46 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.571-6760A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171183 | |||||||
| chr7:26171267 | T | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG00738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.571-6676T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171267 | |||||||
| chr7:26171268 | G | C | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-6675G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171268 | |||||||
| chr7:26171286 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0167 |
7 | HG00597.hp1 NA18946.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-6657C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171286 | |||||||
| chr7:26171379 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.571-6564A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171379 | |||||||
| chr7:26171392 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.571-6551A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171392 | |||||||
| chr7:26171436 | C | T | 1 | a0001c0002t0002g0213 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.571-6507C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171436 | |||||||
| chr7:26171709 | T | A | 7 | a0001c0002t0001g0025 a0001c0002t0001g0074 a0001c0002t0001g0075 others(4): Show |
8 | HG02145.hp1 HG02717.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-6234T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171709 | |||||||
| chr7:26171770 | C | G | 1 | a0003c0003t0003g0193 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.571-6173C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171770 | |||||||
| chr7:26171773 | A | G | 2 | a0001c0002t0015g0087 a0001c0002t0015g0226 |
2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-6170A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171773 | |||||||
| chr7:26171851 | C | CA | 4 | a0001c0001t0001g0148 a0001c0001t0001g0170 a0001c0002t0002g0021 others(1): Show |
6 | HG02572.hp1 NA18747.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-6084dupA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26171851 | ||||||
| chr7:26171922 | C | T | 1 | a0001c0001t0005g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.571-6021C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26171922 | |||||||
| chr7:26172003 | T | C | 5 | a0001c0001t0001g0065 a0001c0002t0008g0024 a0001c0002t0008g0054 others(2): Show |
6 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-5940T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172003 | |||||||
| chr7:26172083 | T | A | 5 | a0001c0001t0001g0065 a0001c0002t0008g0024 a0001c0002t0008g0054 others(2): Show |
6 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-5860T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172083 | |||||||
| chr7:26172154 | C | T | 34 | a0001c0002t0001g0210 a0001c0002t0002g0002 a0001c0002t0002g0008 others(31): Show |
71 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(68): Show |
intron_variant | MODIFIER | c.571-5789C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172154 | |||||||
| chr7:26172162 | G | T | 5 | a0001c0001t0001g0065 a0001c0002t0008g0024 a0001c0002t0008g0054 others(2): Show |
6 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-5781G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172162 | |||||||
| chr7:26172163 | C | A | 1 | a0001c0001t0001g0012 | 4 | HG03209.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-5780C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172163 | |||||||
| chr7:26172195 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.571-5748G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172195 | |||||||
| chr7:26172261 | G | A | 1 | a0001c0002t0002g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.571-5682G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172261 | |||||||
| chr7:26172431 | T | C | 1 | a0001c0002t0004g0149 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.571-5512T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172431 | |||||||
| chr7:26172433 | A | C | 1 | a0001c0002t0001g0042 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.571-5510A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172433 | |||||||
| chr7:26172562 | G | A | 67 | a0001c0001t0001g0065 a0001c0001t0001g0179 a0001c0002t0001g0009 others(64): Show |
97 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.571-5381G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172562 | |||||||
| chr7:26172709 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.571-5234T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172709 | |||||||
| chr7:26172771 | G | T | 2 | a0001c0001t0013g0067 a0001c0001t0013g0141 |
2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.571-5172G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172771 | |||||||
| chr7:26172842 | C | T | 4 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-5101C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172842 | |||||||
| chr7:26172851 | T | G | 52 | a0001c0001t0001g0065 a0001c0001t0001g0179 a0001c0002t0001g0017 others(49): Show |
76 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.571-5092T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26172851 | |||||||
| chr7:26173234 | C | T | 1 | a0001c0002t0001g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.571-4709C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173234 | |||||||
| chr7:26173286 | A | C | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.571-4657A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173286 | |||||||
| chr7:26173388 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0086 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.571-4547_571-4536d others(14): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26173388 | ||||||
| chr7:26173544 | A | C | 1 | a0001c0002t0001g0064 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.571-4399A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173544 | |||||||
| chr7:26173776 | G | A | 34 | a0001c0002t0001g0210 a0001c0002t0002g0002 a0001c0002t0002g0008 others(31): Show |
71 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(68): Show |
intron_variant | MODIFIER | c.571-4167G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173776 | |||||||
| chr7:26173914 | T | G | 1 | a0001c0001t0005g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.571-4029T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26173914 | |||||||
| chr7:26174160 | A | G | 6 | a0001c0001t0005g0070 a0001c0001t0005g0104 a0002c0004t0005g0022 others(3): Show |
9 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-3783A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174160 | |||||||
| chr7:26174162 | C | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0138 others(9): Show |
24 | HG00423.hp1 HG01256.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.571-3781C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174162 | |||||||
| chr7:26174210 | G | T | 2 | a0001c0002t0015g0087 a0001c0002t0015g0226 |
2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-3733G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174210 | |||||||
| chr7:26174285 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.571-3658A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174285 | |||||||
| chr7:26174477 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.571-3466A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174477 | |||||||
| chr7:26174568 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.571-3375G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174568 | |||||||
| chr7:26174611 | A | G | 1 | a0001c0002t0004g0106 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.571-3332A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174611 | |||||||
| chr7:26174707 | G | T | 102 | a0001c0001t0001g0179 a0001c0002t0001g0009 a0001c0002t0001g0017 others(99): Show |
169 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.571-3236G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174707 | |||||||
| chr7:26174799 | G | T | 6 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(3): Show |
7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3144G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174799 | |||||||
| chr7:26174800 | A | T | 6 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(3): Show |
7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-3143A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174800 | |||||||
| chr7:26174869 | T | A | 1 | a0001c0002t0001g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.571-3074T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174869 | |||||||
| chr7:26174894 | A | C | 1 | a0001c0002t0015g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571-3049A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26174894 | |||||||
| chr7:26175121 | C | G | 6 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(3): Show |
7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-2822C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175121 | |||||||
| chr7:26175174 | G | A | 28 | a0001c0001t0001g0179 a0001c0002t0001g0017 a0001c0002t0001g0025 others(25): Show |
40 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.571-2769G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175174 | |||||||
| chr7:26175192 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.571-2751C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175192 | |||||||
| chr7:26175192 | C | CA | 100 | a0001c0001t0001g0062 a0001c0001t0001g0122 a0001c0001t0001g0125 others(97): Show |
167 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.571-2732dupA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175192 | ||||||
| chr7:26175192 | CA | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0052 others(7): Show |
13 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.571-2732delA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175192 | ||||||
| chr7:26175217 | G | A | 1 | a0001c0002t0002g0014 | 4 | NA18612.hp2 NA19070.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-2726G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175217 | |||||||
| chr7:26175233 | A | G | 102 | a0001c0001t0001g0179 a0001c0002t0001g0009 a0001c0002t0001g0017 others(99): Show |
169 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.571-2710A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175233 | |||||||
| chr7:26175252 | T | C | 6 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(3): Show |
7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-2691T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175252 | |||||||
| chr7:26175268 | G | A | 6 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(3): Show |
7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-2675G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175268 | |||||||
| chr7:26175407 | T | C | 1 | a0001c0002t0002g0208 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.571-2536T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175407 | |||||||
| chr7:26175486 | T | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(40): Show |
67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.571-2457T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175486 | |||||||
| chr7:26175495 | C | T | 2 | a0001c0002t0003g0188 a0001c0002t0003g0189 |
2 | HG00438.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.571-2448C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175495 | |||||||
| chr7:26175496 | C | T | 2 | a0001c0002t0003g0188 a0001c0002t0003g0189 |
2 | HG00438.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.571-2447C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175496 | |||||||
| chr7:26175515 | C | T | 10 | a0001c0002t0002g0008 a0001c0002t0002g0014 a0001c0002t0002g0020 others(7): Show |
23 | HG02135.hp1 HG03239.hp1 HG04184.hp2 others(20): Show |
intron_variant | MODIFIER | c.571-2428C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175515 | |||||||
| chr7:26175543 | C | T | 6 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(3): Show |
7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-2400C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175543 | |||||||
| chr7:26175687 | G | A | 2 | a0001c0002t0002g0039 a0001c0002t0017g0039 |
2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.571-2256G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175687 | |||||||
| chr7:26175728 | A | T | 1 | a0001c0002t0014g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-2215A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175728 | |||||||
| chr7:26175750 | G | T | 1 | a0001c0002t0014g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-2193G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175750 | |||||||
| chr7:26175751 | C | T | 1 | a0001c0002t0014g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-2192C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175751 | |||||||
| chr7:26175778 | C | CA | 45 | a0001c0001t0001g0049 a0001c0001t0001g0062 a0001c0001t0001g0090 others(42): Show |
83 | HG00544.hp2 HG00639.hp1 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.571-2149dupA | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175778 | ||||||
| chr7:26175794 | A | T | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-2149A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175794 | |||||||
| chr7:26175795 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.571-2148T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175795 | |||||||
| chr7:26175822 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.571-2121T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175822 | |||||||
| chr7:26175848 | C | A | 4 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-2095C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175848 | |||||||
| chr7:26175853 | C | CT | 32 | a0001c0001t0001g0026 a0001c0001t0001g0081 a0001c0001t0001g0082 others(29): Show |
42 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.571-2071dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175853 | ||||||
| chr7:26175853 | CT | C | 74 | a0001c0001t0001g0136 a0001c0001t0001g0167 a0001c0001t0001g0179 others(71): Show |
129 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.571-2071delT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26175853 | ||||||
| chr7:26175928 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0083 a0001c0001t0001g0097 others(4): Show |
8 | HG01081.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-2015T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175928 | |||||||
| chr7:26175964 | C | T | 1 | a0002c0007t0003g0191 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.571-1979C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175964 | |||||||
| chr7:26175999 | T | A | 3 | a0001c0002t0002g0015 a0001c0002t0002g0202 a0001c0002t0002g0215 |
6 | NA18747.hp2 NA18947.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1944T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26175999 | |||||||
| chr7:26176005 | T | C | 3 | a0001c0002t0002g0015 a0001c0002t0002g0202 a0001c0002t0002g0215 |
6 | NA18747.hp2 NA18947.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1938T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176005 | |||||||
| chr7:26176027 | C | A | 1 | a0001c0002t0002g0047 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.571-1916C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176027 | |||||||
| chr7:26176036 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG00738.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.571-1907C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176036 | |||||||
| chr7:26176053 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.571-1890G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176053 | |||||||
| chr7:26176067 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-1876T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176067 | |||||||
| chr7:26176354 | A | G | 7 | a0001c0001t0001g0065 a0001c0002t0008g0024 a0001c0002t0008g0054 others(4): Show |
8 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-1589A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176354 | |||||||
| chr7:26176474 | G | GGCCGGGC others(32): Show |
1 | a0001c0001t0001g0166 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.571-1436_571-1398d others(41): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176474 | ||||||
| chr7:26176474 | GGCCGGGC others(32): Show |
G | 60 | a0001c0001t0001g0179 a0001c0002t0001g0017 a0001c0002t0001g0025 others(57): Show |
109 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.571-1436_571-1398d others(41): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176474 | ||||||
| chr7:26176474 | GGCCGGGC others(145): Show |
G | 1 | a0001c0002t0002g0211 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.571-1436_571-1285d others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176474 | ||||||
| chr7:26176478 | G | GGGCAGAG others(106): Show |
24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0030 others(21): Show |
42 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.571-1294_571-1182d others(115): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176478 | ||||||
| chr7:26176512 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1431C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176512 | |||||||
| chr7:26176513 | A | G | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1430A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176513 | |||||||
| chr7:26176517 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1426G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176517 | |||||||
| chr7:26176517 | G | GGGCAGAG others(30): Show |
4 | a0001c0002t0003g0013 a0001c0002t0003g0188 a0001c0002t0003g0189 others(1): Show |
7 | HG00438.hp2 HG00733.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-1407_571-1371d others(39): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176517 | ||||||
| chr7:26176536 | A | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(40): Show |
67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.571-1407A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176536 | |||||||
| chr7:26176545 | G | A | 1 | a0001c0002t0014g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.571-1398G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176545 | |||||||
| chr7:26176549 | T | C | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1394T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176549 | |||||||
| chr7:26176550 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1393G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176550 | |||||||
| chr7:26176554 | A | G | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1389A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176554 | |||||||
| chr7:26176573 | T | A | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1370T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176573 | |||||||
| chr7:26176573 | TTCCCAGA others(69): Show |
T | 1 | a0001c0001t0001g0095 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.571-1333_571-1258d others(78): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176573 | ||||||
| chr7:26176586 | T | C | 1 | a0002c0004t0009g0036 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.571-1357T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176586 | |||||||
| chr7:26176591 | A | G | 2 | a0001c0001t0001g0001 a0002c0004t0009g0036 |
4 | HG01255.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1352A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176591 | |||||||
| chr7:26176601 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.571-1342G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176601 | |||||||
| chr7:26176610 | A | T | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1333A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176610 | |||||||
| chr7:26176619 | G | C | 1 | a0013c0017t0001g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1324G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176619 | |||||||
| chr7:26176625 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1318C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176625 | |||||||
| chr7:26176626 | A | G | 4 | a0001c0002t0001g0078 a0001c0002t0002g0002 a0001c0002t0002g0165 others(1): Show |
10 | HG01255.hp2 HG01346.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.571-1317A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176626 | |||||||
| chr7:26176630 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1313G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176630 | |||||||
| chr7:26176630 | GGGCAGAG others(67): Show |
G | 1 | a0001c0002t0002g0002 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.571-1284_571-1211d others(76): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176630 | ||||||
| chr7:26176640 | G | A | 2 | a0001c0001t0001g0004 a0015c0013t0001g0094 |
2 | HG00609.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.571-1303G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176640 | |||||||
| chr7:26176649 | A | ATCCCAGA others(106): Show |
1 | a0004c0006t0012g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.571-1220_571-1108d others(115): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176649 | ||||||
| chr7:26176649 | A | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0002t0001g0078 |
3 | HG01243.hp1 HG01891.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.571-1294A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176649 | |||||||
| chr7:26176649 | ATCCCAGA others(30): Show |
A | 2 | a0001c0001t0001g0085 a0001c0001t0025g0006 |
2 | HG00323.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.571-1257_571-1221d others(39): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176649 | ||||||
| chr7:26176675 | GCGCTCCT others(490): Show |
G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0178 |
2 | HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.571-1253_571-757de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176675 | ||||||
| chr7:26176686 | T | A | 2 | a0001c0002t0001g0078 a0001c0002t0003g0013 |
2 | HG01891.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.571-1257T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176686 | |||||||
| chr7:26176694 | C | CAA | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1249_571-1248i others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176694 | |||||||
| chr7:26176695 | G | T | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1248G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176695 | |||||||
| chr7:26176699 | T | C | 2 | a0001c0001t0001g0004 a0001c0002t0001g0078 |
2 | HG01891.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.571-1244T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176699 | |||||||
| chr7:26176700 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1243G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176700 | |||||||
| chr7:26176704 | A | AGGCAGAG others(69): Show |
1 | a0001c0001t0001g0166 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.571-1221_571-1220i others(78): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176704 | ||||||
| chr7:26176704 | A | G | 5 | a0001c0002t0001g0078 a0001c0002t0008g0024 a0001c0002t0008g0054 others(2): Show |
6 | HG01099.hp2 HG01517.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1239A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176704 | |||||||
| chr7:26176704 | AGGCAGAG others(32): Show |
A | 1 | a0013c0017t0001g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1220_571-1182d others(41): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176704 | ||||||
| chr7:26176720 | C | T | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1223C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176720 | |||||||
| chr7:26176723 | A | T | 4 | a0001c0002t0001g0057 a0001c0002t0014g0066 a0001c0002t0015g0087 others(1): Show |
4 | HG02486.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1220A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176723 | |||||||
| chr7:26176732 | G | A | 2 | a0001c0002t0001g0057 a0001c0002t0014g0066 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.571-1211G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176732 | |||||||
| chr7:26176735 | G | GGGCAGCC others(183): Show |
1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-1182_571-1181i others(192): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176735 | ||||||
| chr7:26176735 | GGGCAGCC others(222): Show |
G | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-1181_571-953de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176735 | ||||||
| chr7:26176738 | C | T | 2 | a0001c0002t0001g0057 a0001c0002t0001g0078 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.571-1205C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176738 | |||||||
| chr7:26176739 | A | G | 2 | a0001c0002t0001g0057 a0001c0002t0001g0078 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.571-1204A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176739 | |||||||
| chr7:26176743 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1200G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176743 | |||||||
| chr7:26176752 | C | T | 17 | a0001c0002t0003g0007 a0001c0002t0003g0013 a0001c0002t0003g0150 others(14): Show |
26 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-1191C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176752 | |||||||
| chr7:26176753 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.571-1190G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176753 | |||||||
| chr7:26176759 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-1184C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176759 | |||||||
| chr7:26176762 | T | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(159): Show |
273 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.571-1181T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176762 | |||||||
| chr7:26176772 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-1171G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176772 | |||||||
| chr7:26176773 | G | T | 1 | a0001c0002t0001g0057 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-1170G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176773 | |||||||
| chr7:26176774 | GTGGCCAG others(183): Show |
G | 1 | a0001c0002t0001g0057 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-1168_571-979de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176774 | |||||||
| chr7:26176780 | AGGCAGAG others(106): Show |
A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0172 |
5 | HG00738.hp1 HG01069.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-1144_571-1032d others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176780 | ||||||
| chr7:26176788 | GCGCTCCT others(377): Show |
G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0033 others(12): Show |
30 | HG00423.hp1 HG01081.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.571-1140_571-757de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176788 | ||||||
| chr7:26176799 | T | A | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1144T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176799 | |||||||
| chr7:26176808 | G | T | 1 | a0013c0017t0001g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1135G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176808 | |||||||
| chr7:26176812 | T | C | 1 | a0001c0002t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-1131T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176812 | |||||||
| chr7:26176817 | A | AGGCAGAG others(32): Show |
4 | a0001c0001t0001g0071 a0001c0001t0001g0105 a0001c0001t0001g0114 others(1): Show |
4 | NA18941.hp1 NA18962.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1108_571-1107i others(41): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176817 | ||||||
| chr7:26176817 | A | C | 4 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-1126A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176817 | |||||||
| chr7:26176817 | A | G | 2 | a0001c0002t0001g0078 a0013c0017t0001g0073 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.571-1126A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176817 | |||||||
| chr7:26176833 | C | T | 1 | a0013c0017t0001g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1110C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176833 | |||||||
| chr7:26176836 | T | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(77): Show |
120 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.571-1107T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176836 | |||||||
| chr7:26176845 | G | A | 63 | a0001c0001t0001g0179 a0001c0002t0001g0017 a0001c0002t0001g0025 others(60): Show |
114 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.571-1098G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176845 | |||||||
| chr7:26176845 | GAT | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0002t0001g0078 |
3 | HG01261.hp1 HG01891.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.571-1097_571-1096d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176845 | |||||||
| chr7:26176847 | T | TGGGCAGC others(30): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0170 others(1): Show |
8 | HG02080.hp2 HG02132.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.571-1093_571-1092i others(39): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176847 | ||||||
| chr7:26176850 | G | T | 1 | a0013c0017t0001g0073 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-1093G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176850 | |||||||
| chr7:26176851 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(73): Show |
112 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.571-1092T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176851 | |||||||
| chr7:26176852 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(73): Show |
112 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.571-1091G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176852 | |||||||
| chr7:26176856 | G | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0157 others(4): Show |
11 | HG01261.hp1 HG01891.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-1087G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176856 | |||||||
| chr7:26176866 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0027 others(143): Show |
239 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.571-1077A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176866 | |||||||
| chr7:26176872 | C | T | 63 | a0001c0001t0001g0179 a0001c0002t0001g0017 a0001c0002t0001g0025 others(60): Show |
114 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.571-1071C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176872 | |||||||
| chr7:26176875 | C | A | 97 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0001t0001g0179 others(94): Show |
163 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.571-1068C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176875 | |||||||
| chr7:26176875 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(44): Show |
73 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.571-1068C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176875 | |||||||
| chr7:26176884 | G | GAT | 4 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0002t0003g0188 others(1): Show |
6 | HG01261.hp1 HG02148.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-1059_571-1058i others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176884 | |||||||
| chr7:26176884 | G | GGGGTGGC others(69): Show |
1 | a0002c0007t0003g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.571-1056_571-1055i others(78): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176884 | ||||||
| chr7:26176885 | G | A | 61 | a0001c0001t0001g0179 a0001c0002t0001g0017 a0001c0002t0001g0025 others(58): Show |
110 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.571-1058G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176885 | |||||||
| chr7:26176886 | G | T | 61 | a0001c0001t0001g0179 a0001c0002t0001g0017 a0001c0002t0001g0025 others(58): Show |
110 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.571-1057G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176886 | |||||||
| chr7:26176887 | GCGGCCGG others(70): Show |
G | 61 | a0001c0001t0001g0179 a0001c0002t0001g0017 a0001c0002t0001g0025 others(58): Show |
110 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.571-1055_571-979de others(78): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176887 | |||||||
| chr7:26176888 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(76): Show |
120 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.571-1055C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176888 | |||||||
| chr7:26176888 | CGGCCGGG others(109): Show |
C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
71 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.571-918_571-803del | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176888 | ||||||
| chr7:26176889 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0002t0003g0188 others(1): Show |
6 | HG01261.hp1 HG02148.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-1054G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176889 | |||||||
| chr7:26176893 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(75): Show |
119 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.571-1050G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176893 | |||||||
| chr7:26176909 | C | T | 1 | a0002c0007t0003g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.571-1034C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176909 | |||||||
| chr7:26176911 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.571-1032C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176911 | |||||||
| chr7:26176912 | A | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(73): Show |
112 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.571-1031A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176912 | |||||||
| chr7:26176921 | G | A | 3 | a0001c0002t0001g0078 a0001c0002t0015g0087 a0001c0002t0015g0226 |
3 | HG01891.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-1022G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176921 | |||||||
| chr7:26176921 | GAT | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(73): Show |
114 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.571-1021_571-1020d others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176921 | |||||||
| chr7:26176927 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(76): Show |
117 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.571-1016C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176927 | |||||||
| chr7:26176928 | G | A | 1 | a0002c0007t0003g0198 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.571-1015G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176928 | |||||||
| chr7:26176932 | A | G | 4 | a0001c0002t0001g0078 a0001c0002t0015g0087 a0001c0002t0015g0226 others(1): Show |
4 | HG01106.hp2 HG01891.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1011A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176932 | |||||||
| chr7:26176940 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(77): Show |
118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.571-1003A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176940 | |||||||
| chr7:26176941 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(77): Show |
118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.571-1002T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176941 | |||||||
| chr7:26176948 | C | T | 3 | a0001c0002t0001g0078 a0001c0002t0015g0087 a0001c0002t0015g0226 |
3 | HG01891.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.571-995C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176948 | |||||||
| chr7:26176951 | T | A | 6 | a0001c0002t0001g0078 a0001c0002t0001g0151 a0001c0002t0015g0087 others(3): Show |
7 | HG01106.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-992T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176951 | |||||||
| chr7:26176955 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(77): Show |
118 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.571-988T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176955 | |||||||
| chr7:26176959 | C | CAA | 28 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(25): Show |
43 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.571-984_571-983ins others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176959 | |||||||
| chr7:26176960 | G | GAT | 43 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(40): Show |
63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.571-983_571-982ins others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176960 | |||||||
| chr7:26176960 | G | T | 28 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(25): Show |
43 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.571-983G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176960 | |||||||
| chr7:26176961 | G | A | 5 | a0001c0002t0001g0078 a0001c0002t0001g0151 a0001c0002t0015g0087 others(2): Show |
6 | HG01891.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-982G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176961 | |||||||
| chr7:26176962 | G | T | 5 | a0001c0002t0001g0078 a0001c0002t0001g0151 a0001c0002t0015g0087 others(2): Show |
6 | HG01891.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-981G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176962 | |||||||
| chr7:26176963 | GT | G | 5 | a0001c0002t0001g0078 a0001c0002t0001g0151 a0001c0002t0015g0087 others(2): Show |
6 | HG01891.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-979delT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176963 | |||||||
| chr7:26176964 | T | TGGCCAGG others(68): Show |
2 | a0001c0002t0011g0019 a0002c0007t0003g0198 |
4 | HG01106.hp2 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-976_571-975ins others(75): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176964 | ||||||
| chr7:26176964 | T | TGGCCGGG others(29): Show |
12 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(9): Show |
18 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-976_571-975ins others(36): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176964 | ||||||
| chr7:26176964 | T | TGGCCGGG others(144): Show |
16 | a0001c0002t0003g0007 a0001c0002t0003g0013 a0001c0002t0003g0150 others(13): Show |
25 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.571-976_571-975ins others(151): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176964 | ||||||
| chr7:26176965 | GGCA | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(40): Show |
63 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.571-975_571-973del others(3): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26176965 | ||||||
| chr7:26176966 | G | T | 60 | a0001c0001t0001g0179 a0001c0002t0001g0017 a0001c0002t0001g0025 others(57): Show |
109 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.571-977G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176966 | |||||||
| chr7:26176967 | C | CCAGGCAG others(142): Show |
1 | a0001c0001t0001g0160 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.571-976_571-975ins others(149): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176967 | |||||||
| chr7:26176967 | C | CCAGGCAG others(29): Show |
1 | a0001c0001t0001g0006 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.571-976_571-975ins others(36): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176967 | |||||||
| chr7:26176968 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0160 |
2 | HG01261.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.571-975A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176968 | |||||||
| chr7:26176971 | C | T | 1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-972C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176971 | |||||||
| chr7:26176982 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(140): Show |
230 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.571-961G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176982 | |||||||
| chr7:26176988 | C | T | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-955C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176988 | |||||||
| chr7:26176991 | A | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(140): Show |
230 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.571-952A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176991 | |||||||
| chr7:26176991 | A | T | 1 | a0004c0006t0012g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.571-952A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26176991 | |||||||
| chr7:26177004 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(141): Show |
231 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.571-939T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177004 | |||||||
| chr7:26177004 | T | TGGCCAGG others(258): Show |
1 | a0001c0002t0001g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.571-935_571-934ins others(265): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177004 | ||||||
| chr7:26177004 | T | TGGCCAGG others(219): Show |
1 | a0002c0004t0009g0036 | 2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.571-935_571-934ins others(226): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177004 | ||||||
| chr7:26177004 | T | TGGCCAGG others(106): Show |
1 | a0004c0006t0012g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.571-935_571-934ins others(113): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177004 | ||||||
| chr7:26177005 | G | A | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-938G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177005 | |||||||
| chr7:26177019 | G | A | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-924G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177019 | |||||||
| chr7:26177028 | A | C | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-915A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177028 | |||||||
| chr7:26177037 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571-906G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177037 | |||||||
| chr7:26177043 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0122 |
2 | HG03831.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.571-900C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177043 | |||||||
| chr7:26177048 | A | G | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-895A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177048 | |||||||
| chr7:26177056 | A | G | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-887A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177056 | |||||||
| chr7:26177057 | T | C | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-886T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177057 | |||||||
| chr7:26177067 | T | A | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-876T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177067 | |||||||
| chr7:26177071 | T | C | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-872T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177071 | |||||||
| chr7:26177077 | G | A | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-866G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177077 | |||||||
| chr7:26177078 | G | T | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-865G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177078 | |||||||
| chr7:26177084 | A | G | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-859A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177084 | |||||||
| chr7:26177084 | AGCCGGGC others(30): Show |
A | 2 | a0001c0002t0002g0008 a0001c0002t0004g0106 |
4 | HG02683.hp1 NA18940.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-839_571-803del others(37): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177084 | ||||||
| chr7:26177088 | G | A | 12 | a0001c0002t0001g0017 a0001c0002t0001g0025 a0001c0002t0001g0074 others(9): Show |
15 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.571-855G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177088 | |||||||
| chr7:26177096 | G | A | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-847G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177096 | |||||||
| chr7:26177097 | C | T | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-846C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177097 | |||||||
| chr7:26177107 | A | T | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-836A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177107 | |||||||
| chr7:26177111 | C | T | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-832C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177111 | |||||||
| chr7:26177134 | C | G | 6 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(3): Show |
7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-809C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177134 | |||||||
| chr7:26177141 | T | C | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-802T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177141 | |||||||
| chr7:26177156 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-787G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177156 | |||||||
| chr7:26177173 | C | T | 6 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(3): Show |
7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-770C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177173 | |||||||
| chr7:26177270 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.571-673C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177270 | |||||||
| chr7:26177410 | A | G | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-533A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177410 | |||||||
| chr7:26177415 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG01346.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.571-528G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177415 | |||||||
| chr7:26177426 | A | G | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-517A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177426 | |||||||
| chr7:26177463 | G | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0110 a0004c0006t0001g0045 others(1): Show |
5 | HG02258.hp1 HG02559.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-480G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177463 | |||||||
| chr7:26177495 | G | GCCGAGGC others(17): Show |
1 | a0001c0001t0001g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.571-437_571-414dup others(24): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 26177495 | ||||||
| chr7:26177590 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.571-353G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177590 | |||||||
| chr7:26177682 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.571-261A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177682 | |||||||
| chr7:26177830 | T | A | 6 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(3): Show |
7 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-113T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177830 | |||||||
| chr7:26177931 | G | T | 1 | a0001c0002t0006g0060 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.571-12G>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 1/3 | chr7 | 26177931 | |||||||
| chr7:26178153 | G | A | 1 | a0001c0005t0001g0156 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.750+31G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178153 | |||||||
| chr7:26178517 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.750+395A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178517 | |||||||
| chr7:26178543 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.750+421G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178543 | |||||||
| chr7:26178692 | GCTGAAGG others(28): Show |
G | 1 | a0001c0002t0002g0213 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.750+573_750+607del others(35): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26178692 | ||||||
| chr7:26178767 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.750+645G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178767 | |||||||
| chr7:26178852 | A | G | 1 | a0001c0002t0001g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.750+730A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178852 | |||||||
| chr7:26178899 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.750+777T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26178899 | |||||||
| chr7:26179038 | C | CTTGA | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.750+918_750+919ins others(4): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26179038 | ||||||
| chr7:26179148 | ATAAATTC others(7): Show |
A | 19 | a0001c0002t0003g0007 a0001c0002t0003g0013 a0001c0002t0003g0150 others(16): Show |
30 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.750+1030_750+1043d others(16): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26179148 | ||||||
| chr7:26179433 | G | A | 1 | a0001c0001t0005g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.750+1311G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179433 | |||||||
| chr7:26179654 | C | T | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.750+1532C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179654 | |||||||
| chr7:26179657 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.750+1535C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179657 | |||||||
| chr7:26179691 | G | GC | 23 | a0001c0002t0001g0017 a0001c0002t0001g0025 a0001c0002t0001g0074 others(20): Show |
35 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.750+1570dupC | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26179691 | ||||||
| chr7:26179776 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.750+1654G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179776 | |||||||
| chr7:26179796 | G | C | 1 | a0001c0001t0019g0127 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.750+1674G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179796 | |||||||
| chr7:26179856 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.750+1734T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179856 | |||||||
| chr7:26179939 | T | C | 27 | a0001c0002t0001g0017 a0001c0002t0001g0025 a0001c0002t0001g0046 others(24): Show |
39 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.750+1817T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179939 | |||||||
| chr7:26179995 | C | T | 3 | a0002c0004t0005g0022 a0002c0004t0005g0041 a0002c0004t0005g0221 |
6 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.750+1873C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26179995 | |||||||
| chr7:26180067 | C | T | 27 | a0001c0002t0001g0017 a0001c0002t0001g0025 a0001c0002t0001g0046 others(24): Show |
39 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.750+1945C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180067 | |||||||
| chr7:26180157 | A | C | 2 | a0001c0002t0008g0024 a0001c0002t0008g0056 |
3 | HG01099.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.750+2035A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180157 | |||||||
| chr7:26180157 | A | G | 2 | a0001c0002t0008g0054 a0001c0002t0008g0055 |
2 | HG01517.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.750+2035A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180157 | |||||||
| chr7:26180690 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.750+2568A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180690 | |||||||
| chr7:26180936 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.751-2765A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180936 | |||||||
| chr7:26180952 | C | T | 1 | a0001c0002t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.751-2749C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26180952 | |||||||
| chr7:26180965 | C | CT | 22 | a0001c0001t0001g0093 a0001c0001t0001g0167 a0001c0001t0018g0192 others(19): Show |
31 | HG00438.hp2 HG00597.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.751-2723dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26180965 | ||||||
| chr7:26181062 | A | C | 2 | a0001c0002t0015g0087 a0001c0002t0015g0226 |
2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.751-2639A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181062 | |||||||
| chr7:26181216 | A | G | 1 | a0001c0002t0015g0087 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.751-2485A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181216 | |||||||
| chr7:26181252 | C | T | 1 | a0001c0002t0002g0014 | 4 | NA18612.hp2 NA19070.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.751-2449C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181252 | |||||||
| chr7:26181560 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.751-2141A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181560 | |||||||
| chr7:26181580 | ATATAAAC others(50): Show |
A | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.751-2119_751-2063d others(59): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26181580 | ||||||
| chr7:26181612 | A | G | 1 | a0001c0002t0008g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.751-2089A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181612 | |||||||
| chr7:26181683 | A | T | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-2018A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181683 | |||||||
| chr7:26181819 | T | C | 3 | a0001c0002t0002g0207 a0001c0002t0002g0209 a0001c0002t0002g0220 |
3 | HG02486.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.751-1882T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181819 | |||||||
| chr7:26181913 | T | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0177 |
2 | HG01081.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.751-1788T>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181913 | |||||||
| chr7:26181989 | A | T | 1 | a0001c0002t0002g0213 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.751-1712A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26181989 | |||||||
| chr7:26182022 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.751-1679A>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182022 | |||||||
| chr7:26182111 | C | T | 33 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0014 others(30): Show |
70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-1590C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182111 | |||||||
| chr7:26182144 | G | GAAACAGA others(12): Show |
1 | a0001c0001t0005g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.751-1554_751-1536d others(21): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182144 | ||||||
| chr7:26182214 | T | G | 1 | a0001c0002t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.751-1487T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182214 | |||||||
| chr7:26182287 | A | G | 1 | a0001c0002t0002g0215 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.751-1414A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182287 | |||||||
| chr7:26182308 | T | C | 1 | a0001c0002t0011g0019 | 3 | HG02451.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.751-1393T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182308 | |||||||
| chr7:26182311 | T | TGAAGCA | 22 | a0001c0002t0002g0002 a0001c0002t0002g0014 a0001c0002t0002g0015 others(19): Show |
49 | HG01255.hp2 HG01346.hp2 HG01496.hp2 others(46): Show |
intron_variant | MODIFIER | c.751-1390_751-1389i others(8): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182311 | |||||||
| chr7:26182311 | T | TGAAGCAT others(6): Show |
53 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0025 others(50): Show |
81 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.751-1390_751-1389i others(15): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182311 | |||||||
| chr7:26182313 | T | G | 75 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0025 others(72): Show |
130 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.751-1388T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182313 | |||||||
| chr7:26182366 | GTAATCCC others(766): Show |
G | 1 | a0001c0001t0001g0158 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.751-1331_751-559de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182366 | ||||||
| chr7:26182368 | A | AATCCCAA others(25): Show |
5 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(2): Show |
9 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.751-1329_751-1298d others(34): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182368 | ||||||
| chr7:26182382 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.751-1319G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182382 | |||||||
| chr7:26182392 | G | A | 1 | a0001c0002t0003g0013 | 4 | HG00741.hp1 HG01106.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.751-1309G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182392 | |||||||
| chr7:26182449 | C | T | 2 | a0001c0002t0002g0039 a0001c0002t0017g0039 |
2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.751-1252C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182449 | |||||||
| chr7:26182454 | G | A | 1 | a0001c0002t0002g0213 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.751-1247G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182454 | |||||||
| chr7:26182470 | A | G | 1 | a0001c0002t0008g0054 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.751-1231A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182470 | |||||||
| chr7:26182475 | T | TTGGCCAG others(57): Show |
7 | a0001c0002t0001g0057 a0001c0002t0001g0058 a0001c0002t0001g0064 others(4): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-1225_751-1162d others(66): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182475 | ||||||
| chr7:26182606 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0224 |
6 | NA18957.hp1 NA18977.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.751-1095C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182606 | |||||||
| chr7:26182618 | A | ACTGTCTC others(62): Show |
1 | a0001c0002t0003g0013 | 3 | HG00741.hp1 HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.751-1082_751-1014d others(71): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182618 | ||||||
| chr7:26182648 | ACTGGGTT others(397): Show |
A | 1 | a0014c0018t0014g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.751-1047_751-644de others(1): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26182648 | ||||||
| chr7:26182652 | G | A | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-1049G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182652 | |||||||
| chr7:26182730 | G | A | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-971G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26182730 | |||||||
| chr7:26183252 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.751-449T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183252 | |||||||
| chr7:26183353 | A | G | 33 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0014 others(30): Show |
70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-348A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183353 | |||||||
| chr7:26183355 | T | C | 33 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0014 others(30): Show |
70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-346T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183355 | |||||||
| chr7:26183363 | C | A | 33 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0014 others(30): Show |
70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-338C>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183363 | |||||||
| chr7:26183368 | T | G | 33 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0014 others(30): Show |
70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-333T>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183368 | |||||||
| chr7:26183369 | G | GCA | 33 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0014 others(30): Show |
70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-332_751-331ins others(2): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183369 | |||||||
| chr7:26183379 | C | G | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-322C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183379 | |||||||
| chr7:26183381 | C | G | 33 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0014 others(30): Show |
70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-320C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183381 | |||||||
| chr7:26183384 | C | G | 33 | a0001c0002t0002g0002 a0001c0002t0002g0008 a0001c0002t0002g0014 others(30): Show |
70 | HG00544.hp2 HG01255.hp2 HG01346.hp2 others(67): Show |
intron_variant | MODIFIER | c.751-317C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183384 | |||||||
| chr7:26183391 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.751-310T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183391 | |||||||
| chr7:26183434 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.751-267G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183434 | |||||||
| chr7:26183440 | CCGGAGGC others(110): Show |
C | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-260_751-144del | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183440 | |||||||
| chr7:26183529 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0033 |
5 | HG01515.hp1 HG01517.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-172G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183529 | |||||||
| chr7:26183540 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0068 a0001c0001t0001g0090 |
5 | HG03831.hp2 NA18966.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-161G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183540 | |||||||
| chr7:26183620 | T | TGATCCTT others(4): Show |
1 | a0003c0003t0003g0190 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.751-77_751-67dupCC others(9): Show |
NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 26183620 | ||||||
| chr7:26183674 | A | G | 98 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0025 others(95): Show |
165 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.751-27A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183674 | |||||||
| chr7:26183698 | C | G | 1 | a0001c0002t0001g0151 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.751-3C>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 2/3 | chr7 | 26183698 | |||||||
| chr7:26183811 | C | T | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.834+27C>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26183811 | |||||||
| chr7:26183986 | A | G | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.834+202A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26183986 | |||||||
| chr7:26183999 | A | T | 4 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(1): Show |
8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.834+215A>T | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26183999 | |||||||
| chr7:26184097 | T | C | 15 | a0001c0002t0001g0009 a0001c0002t0001g0042 a0001c0002t0001g0044 others(12): Show |
21 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.834+313T>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184097 | |||||||
| chr7:26184386 | A | AT | 100 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0025 others(97): Show |
167 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.835-144dupT | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 26184386 | ||||||
| chr7:26184395 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.835-138G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184395 | |||||||
| chr7:26184454 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.835-79G>C | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184454 | |||||||
| chr7:26184478 | A | G | 11 | a0001c0002t0001g0017 a0001c0002t0001g0025 a0001c0002t0001g0074 others(8): Show |
14 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.835-55A>G | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184478 | |||||||
| chr7:26184508 | G | A | 4 | a0001c0002t0008g0024 a0001c0002t0008g0054 a0001c0002t0008g0055 others(1): Show |
5 | HG01099.hp2 HG01517.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-25G>A | NFE2L3 | ENSG00000050344.9 | transcript | ENST00000056233.4 | protein_coding | 3/3 | chr7 | 26184508 |