Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4780 |
| ensemblid | ENSG00000116044.17 |
| hgncid | 7782 |
| symbol | NFE2L2 |
| name | NFE2 like bZIP transcription factor 2 |
| refseq_nuc | NM_006164.5 |
| refseq_prot | NP_006155.2 |
| ensembl_nuc | ENST00000397062.8 |
| ensembl_prot | ENSP00000380252.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 177230308 |
| end | 177264727 |
| strand | - |
| ver | v1.2 |
| region | chr2:177230308-177264727 |
| region5000 | chr2:177225308-177269727 |
| regionname0 | NFE2L2_chr2_177230308_177264727 |
| regionname5000 | NFE2L2_chr2_177225308_177269727 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 605 | 320 | 90 | 70 | 120 | 14 | 24 | 86 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | MMDLE others(600): Show |
chr2 | 177225308 | 177269727 |
| a0002 | 0/0 | 605 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | MMDLE others(600): Show |
chr2 | 177225308 | 177269727 |
| a0003 | 0/0 | 605 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | MMDLE others(600): Show |
chr2 | 177225308 | 177269727 |
| a0004 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | MMDLE others(600): Show |
chr2 | 177225308 | 177269727 |
| a0005 | 0/0 | 605 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | MMDLE others(600): Show |
chr2 | 177225308 | 177269727 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1815 | 319 | 90 | 69 | 120 | 14 | 24 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | ATGAT others(1810): Show |
chr2 | 177225308 | 177269727 | ||
| a0001c0005 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | ATGAT others(1810): Show |
chr2 | 177225308 | 177269727 | ||
| a0002c0002 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | ATGAT others(1810): Show |
chr2 | 177225308 | 177269727 | ||
| a0003c0003 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | ATGAT others(1810): Show |
chr2 | 177225308 | 177269727 | ||
| a0004c0004 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | ATGAT others(1810): Show |
chr2 | 177225308 | 177269727 | ||
| a0005c0006 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | ATGAT others(1810): Show |
chr2 | 177225308 | 177269727 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2446 | 182 | 53 | 43 | 65 | 7 | 12 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0002 | 0/0 | 2443 | 102 | 13 | 21 | 49 | 7 | 12 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2438): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0003 | 0/0 | 2437 | 8 | 8 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2432): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0004 | 0/0 | 2445 | 5 | 0 | 4 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2440): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0005 | 0/0 | 2446 | 6 | 6 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0006 | 0/0 | 2442 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2437): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0007 | 0/0 | 2446 | 4 | 4 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0008 | 0/0 | 2443 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2438): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0009 | 0/0 | 2446 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0010 | 0/0 | 2446 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0011 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2432): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0012 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2438): Show |
chr2 | 177225308 | 177269727 |
| a0001c0001t0013 | 0/0 | 2446 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| a0001c0005t0001 | 0/0 | 2446 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| a0002c0002t0001 | 0/0 | 2446 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| a0003c0003t0001 | 0/0 | 2446 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| a0003c0003t0004 | 0/0 | 2445 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2440): Show |
chr2 | 177225308 | 177269727 |
| a0004c0004t0002 | 0/0 | 2443 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2438): Show |
chr2 | 177225308 | 177269727 |
| a0005c0006t0001 | 0/0 | 2446 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | GATTA others(2441): Show |
chr2 | 177225308 | 177269727 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0005 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0018 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0001 | 0/0 | 30 | 0 | 5 | 20 | 1 | 4 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0006g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0007g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0008g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0009g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0010g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0001t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0001c0005t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0002c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0003c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0003c0003t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0004c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| a0005c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | GBR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0065 | EUR | FIN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | FIN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00735 | hp1 | a0001 | c0001 | t0010 | g0038 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00738 | hp1 | a0001 | c0005 | t0001 | g0126 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0149 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CDX | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CDX | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0169 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02897 | hp1 | a0003 | c0003 | t0004 | g0170 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0203 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0206 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0135 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | CHB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18951 | hp2 | a0004 | c0004 | t0002 | g0072 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18968 | hp2 | a0001 | c0001 | t0012 | g0076 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19000 | hp1 | a0005 | c0006 | t0001 | g0157 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0046 | AFR | YRI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ASW | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ASW | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | USA | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | USA | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | USA | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | USA | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0166 | REF | REF | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | NFE2L2_chr2_177225308_177269727 | NFE2L2 | chr2 | 177225308 | 177269727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:177231257 | C | T | 1 | a0004 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.1346G>A | p.Arg449His | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 1497/2446 | 1346/1818 | 449/605 | chr2 | 177231257 | |||
| chr2:177231906 | G | A | 1 | a0005 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.697C>T | p.Pro233Ser | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 848/2446 | 697/1818 | 233/605 | chr2 | 177231906 | |||
| chr2:177231947 | T | C | 1 | a0003 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.656A>G | p.Lys219Arg | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 807/2446 | 656/1818 | 219/605 | chr2 | 177231947 | |||
| chr2:177234189 | C | T | 1 | a0002 | 2 | HG02257.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.128G>A | p.Arg43Gln | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/5 | 279/2446 | 128/1818 | 43/605 | chr2 | 177234189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:177231559 | T | C | 1 | a0001c0005 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.1044A>G | p.Leu348Leu | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 1195/2446 | 1044/1818 | 348/605 | chr2 | 177231559 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:177230317 | C | T | 1 | a0001c0001t0007 | 4 | HG02280.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*468G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 468 | chr2 | 177230317 | ||||||
| chr2:177230350 | AT | A | 3 | a0001c0001t0004 a0001c0001t0006 a0003c0003t0004 |
10 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*434delA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 434 | chr2 | 177230350 | ||||||
| chr2:177230374 | A | C | 1 | a0001c0001t0012 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*411T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 411 | chr2 | 177230374 | ||||||
| chr2:177230431 | T | C | 1 | a0001c0001t0013 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 354 | chr2 | 177230431 | ||||||
| chr2:177230617 | T | C | 2 | a0001c0001t0008 a0001c0001t0009 |
4 | HG02280.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*168A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 168 | chr2 | 177230617 | ||||||
| chr2:177230697 | T | C | 1 | a0001c0001t0011 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 88 | chr2 | 177230697 | ||||||
| chr2:177230767 | G | C | 2 | a0001c0001t0005 a0001c0001t0010 |
7 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*18C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 5/5 | 18 | chr2 | 177230767 | ||||||
| chr2:177264662 | TGGC | T | 5 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(2): Show |
110 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-89_-87delGCC | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/5 | 87 | chr2 | 177264662 | ||||||
| chr2:177264662 | TGGCGGCG others(2): Show |
T | 2 | a0001c0001t0003 a0001c0001t0011 |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-95_-87delGCCGCCGC others(1): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/5 | 87 | chr2 | 177264662 | ||||||
| chr2:177264684 | G | T | 1 | a0001c0001t0010 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/5 | 108 | chr2 | 177264684 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:177232109 | T | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0082 |
2 | HG00609.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.595-101A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 4/4 | chr2 | 177232109 | |||||||
| chr2:177232111 | T | G | 5 | a0001c0001t0005g0020 a0001c0001t0005g0135 a0001c0001t0005g0199 others(2): Show |
7 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.595-103A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 4/4 | chr2 | 177232111 | |||||||
| chr2:177232688 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.403-105G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232688 | |||||||
| chr2:177232704 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.403-121G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232704 | |||||||
| chr2:177232740 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.403-157A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232740 | |||||||
| chr2:177232764 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.403-181T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232764 | |||||||
| chr2:177232817 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.403-234C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232817 | |||||||
| chr2:177232859 | C | G | 2 | a0001c0001t0002g0013 a0001c0001t0002g0099 |
4 | HG01167.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-276G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232859 | |||||||
| chr2:177232936 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.402+314G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232936 | |||||||
| chr2:177232938 | C | T | 50 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(47): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.402+312G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177232938 | |||||||
| chr2:177233064 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0002g0057 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.402+186A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 3/4 | chr2 | 177233064 | |||||||
| chr2:177233359 | CA | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0110 others(3): Show |
9 | HG00140.hp2 HG00733.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-21delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233359 | |||||||
| chr2:177233364 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0013g0206 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.313-25C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233364 | |||||||
| chr2:177233582 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.313-243G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233582 | |||||||
| chr2:177233774 | G | T | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.312+231C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233774 | |||||||
| chr2:177233932 | C | T | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.312+73G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233932 | |||||||
| chr2:177233951 | C | T | 10 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(7): Show |
10 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+54G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233951 | |||||||
| chr2:177233994 | G | A | 3 | a0001c0001t0003g0040 a0001c0001t0003g0042 a0001c0001t0003g0044 |
3 | HG02145.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.312+11C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 2/4 | chr2 | 177233994 | |||||||
| chr2:177234345 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-74G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234345 | |||||||
| chr2:177234532 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0209 |
2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-261C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234532 | |||||||
| chr2:177234605 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.46-334A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234605 | |||||||
| chr2:177234735 | T | C | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-464A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234735 | |||||||
| chr2:177234794 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.46-523G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234794 | |||||||
| chr2:177234802 | T | A | 1 | a0001c0001t0002g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.46-531A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234802 | |||||||
| chr2:177234884 | G | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(92): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.46-613C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234884 | |||||||
| chr2:177234925 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.46-654C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234925 | |||||||
| chr2:177234987 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.46-716C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177234987 | |||||||
| chr2:177235040 | C | T | 1 | a0001c0001t0013g0206 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.46-769G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235040 | |||||||
| chr2:177235047 | G | A | 4 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-776C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235047 | |||||||
| chr2:177235070 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-799A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235070 | |||||||
| chr2:177235164 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0209 |
2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-893C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235164 | |||||||
| chr2:177235169 | C | T | 7 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-898G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235169 | |||||||
| chr2:177235187 | A | G | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-916T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235187 | |||||||
| chr2:177235275 | AAAC | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0173 a0001c0001t0013g0206 |
3 | HG02976.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.46-1007_46-1005del others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235275 | |||||||
| chr2:177235342 | T | TA | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-1072dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235342 | |||||||
| chr2:177235362 | A | G | 5 | a0001c0001t0005g0020 a0001c0001t0005g0135 a0001c0001t0005g0199 others(2): Show |
7 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-1091T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235362 | |||||||
| chr2:177235694 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.46-1423T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235694 | |||||||
| chr2:177235697 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(169): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.46-1426G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235697 | |||||||
| chr2:177235740 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.46-1469A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177235740 | |||||||
| chr2:177236007 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.46-1736C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236007 | |||||||
| chr2:177236080 | A | G | 8 | a0001c0001t0001g0137 a0001c0001t0001g0219 a0001c0001t0003g0040 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-1809T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236080 | |||||||
| chr2:177236464 | A | G | 2 | a0003c0003t0001g0169 a0003c0003t0004g0170 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.46-2193T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236464 | |||||||
| chr2:177236486 | T | C | 14 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(11): Show |
16 | HG01081.hp1 HG01109.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-2215A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236486 | |||||||
| chr2:177236507 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(87): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.46-2236G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236507 | |||||||
| chr2:177236598 | A | G | 7 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-2327T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236598 | |||||||
| chr2:177236599 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.46-2328G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236599 | |||||||
| chr2:177236833 | G | T | 14 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(11): Show |
16 | HG01081.hp1 HG01109.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-2562C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177236833 | |||||||
| chr2:177237035 | C | A | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-2764G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237035 | |||||||
| chr2:177237048 | T | C | 6 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0052 others(3): Show |
6 | HG02145.hp2 HG02572.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-2777A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237048 | |||||||
| chr2:177237222 | G | A | 21 | a0001c0001t0001g0171 a0001c0001t0001g0209 a0001c0001t0001g0215 others(18): Show |
25 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.46-2951C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237222 | |||||||
| chr2:177237527 | AT | A | 19 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(16): Show |
23 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.46-3257delA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237527 | |||||||
| chr2:177237557 | C | T | 7 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-3286G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237557 | |||||||
| chr2:177237950 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.46-3679T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237950 | |||||||
| chr2:177237969 | G | T | 7 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-3698C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177237969 | |||||||
| chr2:177238275 | ATCT | A | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-4007_46-4005del others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238275 | |||||||
| chr2:177238501 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(88): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.46-4230T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238501 | |||||||
| chr2:177238600 | C | T | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-4329G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238600 | |||||||
| chr2:177238609 | T | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0209 |
2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-4338A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238609 | |||||||
| chr2:177238664 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0209 |
2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-4393C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238664 | |||||||
| chr2:177238786 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.46-4515G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177238786 | |||||||
| chr2:177239175 | T | C | 1 | a0001c0001t0002g0078 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.46-4904A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239175 | |||||||
| chr2:177239366 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.46-5095G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239366 | |||||||
| chr2:177239378 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-5107A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239378 | |||||||
| chr2:177239513 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46-5242G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239513 | |||||||
| chr2:177239681 | AAAAGTTT others(37): Show |
A | 1 | a0001c0001t0001g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.46-5454_46-5411del others(44): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239681 | |||||||
| chr2:177239717 | T | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG00735.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.46-5446A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239717 | |||||||
| chr2:177239949 | T | TA | 18 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0143 others(15): Show |
31 | HG00544.hp2 HG00642.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.46-5679dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239949 | |||||||
| chr2:177239949 | TA | T | 161 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(158): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.46-5679delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239949 | |||||||
| chr2:177239949 | TAA | T | 6 | a0001c0001t0001g0121 a0001c0001t0001g0184 a0001c0001t0002g0061 others(3): Show |
6 | HG01106.hp2 HG01167.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-5680_46-5679del others(2): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177239949 | |||||||
| chr2:177240032 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG02523.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.46-5761T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240032 | |||||||
| chr2:177240270 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.46-5999G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240270 | |||||||
| chr2:177240311 | G | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.46-6040C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240311 | |||||||
| chr2:177240416 | A | G | 166 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(163): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.46-6145T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240416 | |||||||
| chr2:177240644 | G | C | 1 | a0001c0001t0002g0079 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.46-6373C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240644 | |||||||
| chr2:177240803 | G | A | 2 | a0001c0001t0002g0087 a0001c0001t0002g0102 |
2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.46-6532C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240803 | |||||||
| chr2:177240948 | A | G | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-6677T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240948 | |||||||
| chr2:177240994 | C | T | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-6723G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177240994 | |||||||
| chr2:177241043 | G | C | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-6772C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241043 | |||||||
| chr2:177241118 | T | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.46-6847A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241118 | |||||||
| chr2:177241268 | C | G | 87 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(84): Show |
146 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.46-6997G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241268 | |||||||
| chr2:177241607 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0209 |
2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.46-7336G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241607 | |||||||
| chr2:177241998 | G | A | 1 | a0001c0001t0013g0206 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.46-7727C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177241998 | |||||||
| chr2:177242030 | A | C | 7 | a0001c0001t0005g0020 a0001c0001t0005g0135 a0001c0001t0005g0199 others(4): Show |
9 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-7759T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242030 | |||||||
| chr2:177242163 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.46-7892A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242163 | |||||||
| chr2:177242234 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0173 a0001c0001t0013g0206 |
3 | HG02818.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.46-7963C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242234 | |||||||
| chr2:177242374 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-8103A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242374 | |||||||
| chr2:177242433 | A | G | 2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.46-8162T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242433 | |||||||
| chr2:177242899 | G | T | 7 | a0001c0001t0005g0020 a0001c0001t0005g0135 a0001c0001t0005g0199 others(4): Show |
9 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-8628C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242899 | |||||||
| chr2:177242900 | T | TG | 6 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8630_46-8629ins others(1): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242900 | |||||||
| chr2:177242908 | T | G | 2 | a0001c0001t0005g0135 a0001c0001t0010g0038 |
2 | HG00735.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.46-8637A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242908 | |||||||
| chr2:177242910 | G | GT | 14 | a0001c0001t0001g0151 a0001c0001t0003g0040 a0001c0001t0003g0041 others(11): Show |
16 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.46-8640dupA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242910 | |||||||
| chr2:177242910 | G | T | 7 | a0001c0001t0005g0020 a0001c0001t0005g0135 a0001c0001t0005g0199 others(4): Show |
9 | HG00735.hp1 HG02717.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-8639C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242910 | |||||||
| chr2:177242990 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.46-8719C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177242990 | |||||||
| chr2:177243150 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.46-8879A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243150 | |||||||
| chr2:177243214 | T | G | 1 | a0001c0001t0001g0027 | 2 | HG00099.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.46-8943A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243214 | |||||||
| chr2:177243227 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.46-8956G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243227 | |||||||
| chr2:177243333 | T | A | 1 | a0001c0001t0001g0029 | 2 | HG00140.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.46-9062A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243333 | |||||||
| chr2:177243421 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46-9150G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243421 | |||||||
| chr2:177243474 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.46-9203C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243474 | |||||||
| chr2:177243522 | A | AT | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-9252dupA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243522 | |||||||
| chr2:177243765 | A | C | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-9494T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243765 | |||||||
| chr2:177243824 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0202 a0001c0001t0001g0204 others(2): Show |
10 | HG01243.hp2 HG02559.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-9553G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243824 | |||||||
| chr2:177243837 | A | G | 1 | a0001c0001t0002g0023 | 2 | HG00323.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.46-9566T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243837 | |||||||
| chr2:177243997 | T | TA | 19 | a0001c0001t0001g0105 a0001c0001t0001g0182 a0001c0001t0003g0040 others(16): Show |
23 | HG00735.hp1 HG01258.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.46-9727dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243997 | |||||||
| chr2:177243997 | TA | T | 6 | a0001c0001t0001g0112 a0001c0001t0001g0140 a0001c0001t0001g0152 others(3): Show |
6 | HG01168.hp2 HG01256.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-9727delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177243997 | |||||||
| chr2:177244038 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.46-9767G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244038 | |||||||
| chr2:177244110 | C | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0218 |
3 | HG00438.hp1 NA18747.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.46-9839G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244110 | |||||||
| chr2:177244187 | G | A | 1 | a0001c0001t0003g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-9916C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244187 | |||||||
| chr2:177244188 | C | G | 1 | a0001c0001t0002g0101 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.46-9917G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244188 | |||||||
| chr2:177244194 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-9923C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244194 | |||||||
| chr2:177244303 | A | C | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-10032T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244303 | |||||||
| chr2:177244367 | C | T | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-10096G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244367 | |||||||
| chr2:177244644 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.46-10373G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244644 | |||||||
| chr2:177244700 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.46-10429C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244700 | |||||||
| chr2:177244706 | A | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0198 a0001c0001t0001g0208 |
4 | HG02818.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-10435T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244706 | |||||||
| chr2:177244777 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.46-10506G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244777 | |||||||
| chr2:177244781 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0212 a0001c0001t0001g0213 others(1): Show |
8 | HG03831.hp2 NA18939.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-10510G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244781 | |||||||
| chr2:177244873 | G | A | 1 | a0001c0001t0002g0099 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.46-10602C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244873 | |||||||
| chr2:177244940 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.46-10669A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177244940 | |||||||
| chr2:177245002 | CA | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.46-10732delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245002 | |||||||
| chr2:177245233 | A | G | 15 | a0001c0001t0001g0034 a0001c0001t0001g0134 a0001c0001t0001g0137 others(12): Show |
17 | HG01361.hp1 HG01884.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-10962T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245233 | |||||||
| chr2:177245241 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-10970C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245241 | |||||||
| chr2:177245396 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.46-11125G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245396 | |||||||
| chr2:177245555 | G | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0112 others(6): Show |
11 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-11284C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245555 | |||||||
| chr2:177245615 | CT | C | 7 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-11345delA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245615 | |||||||
| chr2:177245902 | G | C | 1 | a0001c0001t0001g0111 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.46-11631C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245902 | |||||||
| chr2:177245923 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46-11652A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177245923 | |||||||
| chr2:177246144 | T | A | 1 | a0001c0001t0001g0172 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.46-11873A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246144 | |||||||
| chr2:177246174 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.46-11903C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246174 | |||||||
| chr2:177246239 | A | T | 7 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-11968T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246239 | |||||||
| chr2:177246403 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.46-12132T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246403 | |||||||
| chr2:177246484 | C | A | 6 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-12213G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246484 | |||||||
| chr2:177246599 | C | CT | 4 | a0001c0001t0001g0195 a0001c0001t0002g0069 a0001c0001t0007g0021 others(1): Show |
6 | HG01071.hp2 HG02280.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-12329dupA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246599 | |||||||
| chr2:177246599 | C | CTT | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-12330_46-12329d others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246599 | |||||||
| chr2:177246608 | C | T | 171 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(168): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.46-12337G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246608 | |||||||
| chr2:177246774 | C | CT | 160 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(157): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.46-12504dupA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246774 | |||||||
| chr2:177246774 | C | CTT | 7 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0173 others(4): Show |
7 | HG01109.hp1 HG01257.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-12505_46-12504d others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246774 | |||||||
| chr2:177246774 | CTTTTTT | C | 13 | a0001c0001t0001g0034 a0001c0001t0001g0137 a0001c0001t0001g0177 others(10): Show |
14 | HG01361.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-12509_46-12504d others(8): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177246774 | |||||||
| chr2:177247365 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG02523.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.46-13094T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247365 | |||||||
| chr2:177247521 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.46-13250G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247521 | |||||||
| chr2:177247576 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.46-13305C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247576 | |||||||
| chr2:177247633 | T | C | 3 | a0001c0001t0005g0020 a0001c0001t0005g0199 a0001c0001t0005g0201 |
5 | HG02717.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-13362A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247633 | |||||||
| chr2:177247684 | C | CA | 17 | a0001c0001t0001g0105 a0001c0001t0001g0117 a0001c0001t0001g0146 others(14): Show |
17 | HG01081.hp1 HG01109.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.46-13414dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247684 | |||||||
| chr2:177247727 | A | G | 7 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-13456T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247727 | |||||||
| chr2:177247867 | G | A | 1 | a0001c0001t0005g0199 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46-13596C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247867 | |||||||
| chr2:177247883 | C | T | 6 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-13612G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247883 | |||||||
| chr2:177247911 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-13640C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247911 | |||||||
| chr2:177247982 | G | A | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-13711C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247982 | |||||||
| chr2:177247994 | A | G | 6 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-13723T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247994 | |||||||
| chr2:177247997 | G | A | 7 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-13726C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177247997 | |||||||
| chr2:177248471 | G | A | 3 | a0001c0001t0005g0020 a0001c0001t0005g0199 a0001c0001t0005g0201 |
5 | HG02717.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-14200C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248471 | |||||||
| chr2:177248476 | C | G | 2 | a0001c0001t0001g0173 a0001c0001t0013g0206 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.46-14205G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248476 | |||||||
| chr2:177248519 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.46-14248G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248519 | |||||||
| chr2:177248538 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-14267A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248538 | |||||||
| chr2:177248556 | T | C | 13 | a0001c0001t0001g0034 a0001c0001t0001g0137 a0001c0001t0001g0177 others(10): Show |
14 | HG01361.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-14285A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248556 | |||||||
| chr2:177248687 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.46-14416C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248687 | |||||||
| chr2:177248756 | A | G | 186 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(183): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.46-14485T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248756 | |||||||
| chr2:177248816 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0151 |
6 | HG00408.hp2 HG02015.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-14545T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248816 | |||||||
| chr2:177248897 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.46-14626G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248897 | |||||||
| chr2:177248922 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0002g0057 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.46-14651G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177248922 | |||||||
| chr2:177249090 | C | T | 2 | a0001c0001t0008g0022 a0001c0001t0009g0032 |
4 | HG02280.hp1 HG02615.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-14819G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249090 | |||||||
| chr2:177249179 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.46-14908T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249179 | |||||||
| chr2:177249217 | C | CATAA | 133 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(130): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.46-14950_46-14947d others(6): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | |||||||
| chr2:177249217 | C | CATAAATA others(1): Show |
6 | a0001c0001t0001g0132 a0001c0001t0001g0171 a0001c0001t0001g0173 others(3): Show |
6 | HG00609.hp1 HG01517.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-14954_46-14947d others(10): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | |||||||
| chr2:177249217 | C | CATAAATA others(5): Show |
8 | a0001c0001t0001g0174 a0001c0001t0004g0028 a0001c0001t0004g0148 others(5): Show |
10 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-14958_46-14947d others(14): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | |||||||
| chr2:177249217 | CATAAATA others(1): Show |
C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | HG01361.hp1 HG01884.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.46-14954_46-14947d others(10): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | |||||||
| chr2:177249217 | CATAAATA others(5): Show |
C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0121 |
4 | HG00733.hp2 HG01175.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-14958_46-14947d others(14): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249217 | |||||||
| chr2:177249376 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.46-15105C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249376 | |||||||
| chr2:177249494 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.45+15038T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249494 | |||||||
| chr2:177249642 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0209 |
2 | HG03704.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.45+14890A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249642 | |||||||
| chr2:177249800 | A | G | 7 | a0001c0001t0004g0028 a0001c0001t0004g0148 a0001c0001t0004g0149 others(4): Show |
9 | HG01257.hp2 HG01258.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+14732T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249800 | |||||||
| chr2:177249904 | A | G | 181 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(178): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.45+14628T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177249904 | |||||||
| chr2:177250012 | C | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0212 a0001c0001t0001g0213 others(1): Show |
8 | HG03831.hp2 NA18939.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+14520G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250012 | |||||||
| chr2:177250082 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.45+14450A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250082 | |||||||
| chr2:177250244 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0013g0206 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.45+14288C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250244 | |||||||
| chr2:177250623 | G | A | 7 | a0001c0001t0001g0215 a0001c0001t0002g0059 a0001c0001t0002g0060 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+13909C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250623 | |||||||
| chr2:177250748 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.45+13784G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250748 | |||||||
| chr2:177250825 | G | T | 6 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+13707C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177250825 | |||||||
| chr2:177251430 | A | G | 4 | a0001c0001t0005g0020 a0001c0001t0005g0199 a0001c0001t0005g0201 others(1): Show |
7 | HG02257.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+13102T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251430 | |||||||
| chr2:177251534 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG01106.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.45+12998T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251534 | |||||||
| chr2:177251600 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.45+12932C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251600 | |||||||
| chr2:177251718 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.45+12814C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251718 | |||||||
| chr2:177251731 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0147 others(2): Show |
11 | HG00558.hp1 HG02523.hp1 NA18949.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+12801G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251731 | |||||||
| chr2:177251787 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.45+12745G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251787 | |||||||
| chr2:177251863 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0120 |
2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.45+12669T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251863 | |||||||
| chr2:177251900 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0202 a0001c0001t0001g0204 others(2): Show |
10 | HG01243.hp2 HG02559.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+12632C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177251900 | |||||||
| chr2:177252000 | C | CA | 39 | a0001c0001t0001g0034 a0001c0001t0001g0134 a0001c0001t0001g0161 others(36): Show |
45 | HG01081.hp1 HG01361.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.45+12531dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252000 | |||||||
| chr2:177252000 | C | CAA | 131 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(128): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.45+12530_45+12531d others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252000 | |||||||
| chr2:177252000 | C | CAAA | 10 | a0001c0001t0001g0016 a0001c0001t0001g0106 a0001c0001t0001g0108 others(7): Show |
13 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+12529_45+12531d others(5): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252000 | |||||||
| chr2:177252021 | AT | A | 7 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(4): Show |
7 | HG00423.hp1 HG02027.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+12510delA | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252021 | |||||||
| chr2:177252209 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45+12323A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252209 | |||||||
| chr2:177252249 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.45+12283G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252249 | |||||||
| chr2:177252660 | T | TC | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.45+11871_45+11872i others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252660 | |||||||
| chr2:177252662 | T | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.45+11870A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252662 | |||||||
| chr2:177252680 | C | T | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+11852G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252680 | |||||||
| chr2:177252887 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.45+11645T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252887 | |||||||
| chr2:177252917 | G | A | 6 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+11615C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252917 | |||||||
| chr2:177252941 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+11591A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252941 | |||||||
| chr2:177252999 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+11533A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177252999 | |||||||
| chr2:177253037 | C | T | 129 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0014 others(126): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.45+11495G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253037 | |||||||
| chr2:177253174 | A | T | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.45+11358T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253174 | |||||||
| chr2:177253277 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.45+11255T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253277 | |||||||
| chr2:177253424 | C | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(28): Show |
41 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.45+11108G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253424 | |||||||
| chr2:177253570 | C | A | 2 | a0001c0001t0001g0171 a0001c0001t0002g0057 |
2 | HG03704.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.45+10962G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253570 | |||||||
| chr2:177253613 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0142 a0001c0001t0001g0143 |
9 | HG00642.hp2 HG01257.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+10919T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253613 | |||||||
| chr2:177253671 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0204 a0001c0001t0001g0205 |
8 | HG01243.hp2 HG02559.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+10861T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253671 | |||||||
| chr2:177253772 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.45+10760T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253772 | |||||||
| chr2:177253822 | C | A | 160 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(157): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.45+10710G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177253822 | |||||||
| chr2:177254262 | A | G | 68 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(65): Show |
85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.45+10270T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254262 | |||||||
| chr2:177254293 | T | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG02486.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.45+10239A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254293 | |||||||
| chr2:177254312 | G | C | 2 | a0001c0001t0001g0171 a0001c0001t0002g0057 |
2 | HG03704.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.45+10220C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254312 | |||||||
| chr2:177254476 | A | C | 48 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.45+10056T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254476 | |||||||
| chr2:177254568 | G | A | 178 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(175): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.45+9964C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254568 | |||||||
| chr2:177254570 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.45+9962C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254570 | |||||||
| chr2:177254585 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.45+9947T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254585 | |||||||
| chr2:177254612 | C | T | 2 | a0001c0001t0001g0174 a0002c0002t0001g0033 |
3 | HG02257.hp1 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.45+9920G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254612 | |||||||
| chr2:177254638 | C | T | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+9894G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254638 | |||||||
| chr2:177254787 | T | C | 12 | a0001c0001t0001g0134 a0001c0001t0001g0171 a0001c0001t0001g0174 others(9): Show |
15 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+9745A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254787 | |||||||
| chr2:177254839 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0197 a0001c0001t0005g0135 |
3 | HG02818.hp1 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.45+9693A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254839 | |||||||
| chr2:177254985 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45+9547A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177254985 | |||||||
| chr2:177255005 | A | G | 1 | a0001c0001t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+9527T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255005 | |||||||
| chr2:177255047 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.45+9485A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255047 | |||||||
| chr2:177255090 | C | T | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+9442G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255090 | |||||||
| chr2:177255097 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+9435G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255097 | |||||||
| chr2:177255108 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45+9424C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255108 | |||||||
| chr2:177255155 | T | C | 1 | a0001c0001t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+9377A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255155 | |||||||
| chr2:177255225 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+9307C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255225 | |||||||
| chr2:177255296 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.45+9236G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255296 | |||||||
| chr2:177255309 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+9223G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255309 | |||||||
| chr2:177255521 | C | A | 1 | a0001c0001t0003g0045 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.45+9011G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255521 | |||||||
| chr2:177255531 | ACCAG | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0162 |
3 | NA18983.hp2 NA18992.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.45+8997_45+9000del others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255531 | |||||||
| chr2:177255584 | T | G | 178 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(175): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.45+8948A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255584 | |||||||
| chr2:177255591 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.45+8941T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255591 | |||||||
| chr2:177255663 | T | C | 177 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(174): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.45+8869A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255663 | |||||||
| chr2:177255697 | T | C | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+8835A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255697 | |||||||
| chr2:177255859 | C | T | 5 | a0001c0001t0001g0200 a0001c0001t0005g0020 a0001c0001t0005g0199 others(2): Show |
7 | HG00735.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+8673G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255859 | |||||||
| chr2:177255938 | G | T | 6 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+8594C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255938 | |||||||
| chr2:177255953 | G | T | 1 | a0001c0001t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+8579C>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177255953 | |||||||
| chr2:177256148 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.45+8384C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256148 | |||||||
| chr2:177256244 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.45+8288T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256244 | |||||||
| chr2:177256277 | C | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.45+8255G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256277 | |||||||
| chr2:177256384 | T | C | 67 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(64): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.45+8148A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256384 | |||||||
| chr2:177256499 | C | CA | 20 | a0001c0001t0001g0109 a0001c0001t0001g0165 a0001c0001t0001g0189 others(17): Show |
27 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.45+8032dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256499 | |||||||
| chr2:177256499 | C | CAA | 43 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(40): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.45+8031_45+8032dup others(2): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256499 | |||||||
| chr2:177256499 | CA | C | 22 | a0001c0001t0001g0034 a0001c0001t0001g0139 a0001c0001t0001g0171 others(19): Show |
24 | HG01168.hp1 HG01361.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.45+8032delT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256499 | |||||||
| chr2:177256649 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+7883T>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256649 | |||||||
| chr2:177256796 | C | A | 47 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(44): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.45+7736G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256796 | |||||||
| chr2:177256925 | C | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(33): Show |
52 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+7607G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256925 | |||||||
| chr2:177256979 | G | A | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+7553C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177256979 | |||||||
| chr2:177257010 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0005g0135 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+7522C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257010 | |||||||
| chr2:177257074 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0005g0135 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+7458G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257074 | |||||||
| chr2:177257153 | T | G | 1 | a0001c0001t0002g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.45+7379A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257153 | |||||||
| chr2:177257175 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.45+7357C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257175 | |||||||
| chr2:177257194 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0005g0135 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+7338T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257194 | |||||||
| chr2:177257465 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.45+7067G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257465 | |||||||
| chr2:177257476 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+7056A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257476 | |||||||
| chr2:177257509 | G | C | 1 | a0001c0001t0002g0096 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.45+7023C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257509 | |||||||
| chr2:177257573 | C | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0049 |
4 | HG00733.hp1 HG01928.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+6959G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257573 | |||||||
| chr2:177257600 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0005g0135 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+6932A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257600 | |||||||
| chr2:177257602 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.45+6930G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257602 | |||||||
| chr2:177257637 | A | C | 58 | a0001c0001t0001g0215 a0001c0001t0002g0001 a0001c0001t0002g0006 others(55): Show |
101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.45+6895T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257637 | |||||||
| chr2:177257676 | T | C | 1 | a0001c0001t0006g0104 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.45+6856A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257676 | |||||||
| chr2:177257731 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.45+6801G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257731 | |||||||
| chr2:177257868 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.45+6664C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257868 | |||||||
| chr2:177257907 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0005g0135 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+6625T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257907 | |||||||
| chr2:177257939 | T | C | 9 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+6593A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257939 | |||||||
| chr2:177257999 | G | A | 43 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.45+6533C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177257999 | |||||||
| chr2:177258177 | ACAACT | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0099 |
4 | HG01167.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+6350_45+6354del others(5): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258177 | |||||||
| chr2:177258274 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+6258C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258274 | |||||||
| chr2:177258345 | T | TGATTCCA others(9): Show |
3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6171_45+6186dup others(16): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258345 | |||||||
| chr2:177258401 | T | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6131A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258401 | |||||||
| chr2:177258455 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+6077A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258455 | |||||||
| chr2:177258633 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0005g0135 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+5899T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258633 | |||||||
| chr2:177258656 | T | C | 2 | a0001c0001t0001g0174 a0002c0002t0001g0033 |
3 | HG02257.hp1 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.45+5876A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258656 | |||||||
| chr2:177258726 | T | A | 1 | a0001c0001t0002g0100 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.45+5806A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258726 | |||||||
| chr2:177258964 | T | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
8 | HG01361.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+5568A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177258964 | |||||||
| chr2:177259139 | T | C | 5 | a0001c0001t0001g0200 a0001c0001t0005g0020 a0001c0001t0005g0199 others(2): Show |
7 | HG00735.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+5393A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259139 | |||||||
| chr2:177259168 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0167 a0001c0001t0001g0168 |
4 | NA18949.hp1 NA18989.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+5364C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259168 | |||||||
| chr2:177259227 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+5305C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259227 | |||||||
| chr2:177259301 | C | A | 9 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+5231G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259301 | |||||||
| chr2:177259346 | TG | T | 3 | a0001c0001t0009g0032 a0003c0003t0001g0169 a0003c0003t0004g0170 |
4 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+5185delC | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259346 | |||||||
| chr2:177259471 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.45+5061C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259471 | |||||||
| chr2:177259609 | TTTTCATG others(26): Show |
T | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+4890_45+4922del others(33): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259609 | |||||||
| chr2:177259658 | C | T | 59 | a0001c0001t0001g0215 a0001c0001t0002g0001 a0001c0001t0002g0006 others(56): Show |
102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.45+4874G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259658 | |||||||
| chr2:177259780 | A | G | 2 | a0001c0001t0002g0057 a0001c0001t0008g0022 |
3 | HG02615.hp1 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.45+4752T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259780 | |||||||
| chr2:177259910 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.45+4622G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259910 | |||||||
| chr2:177259911 | G | A | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+4621C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177259911 | |||||||
| chr2:177260059 | A | G | 59 | a0001c0001t0001g0215 a0001c0001t0002g0001 a0001c0001t0002g0006 others(56): Show |
102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.45+4473T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260059 | |||||||
| chr2:177260140 | T | C | 1 | a0001c0001t0001g0010 | 4 | HG00280.hp1 HG01261.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+4392A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260140 | |||||||
| chr2:177260375 | A | G | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+4157T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260375 | |||||||
| chr2:177260414 | A | G | 43 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.45+4118T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260414 | |||||||
| chr2:177260800 | A | G | 43 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(40): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.45+3732T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260800 | |||||||
| chr2:177260807 | G | GCAAA | 105 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(102): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.45+3724_45+3725ins others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260807 | |||||||
| chr2:177260835 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0005g0135 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45+3697G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260835 | |||||||
| chr2:177260895 | G | A | 9 | a0001c0001t0001g0171 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
11 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+3637C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260895 | |||||||
| chr2:177260994 | G | A | 37 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(34): Show |
53 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.45+3538C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177260994 | |||||||
| chr2:177261170 | C | CA | 12 | a0001c0001t0001g0107 a0001c0001t0001g0172 a0001c0001t0001g0173 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+3361dupT | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261170 | |||||||
| chr2:177261170 | C | CAA | 45 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(42): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.45+3360_45+3361dup others(2): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261170 | |||||||
| chr2:177261170 | C | CAAA | 42 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(39): Show |
60 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.45+3359_45+3361dup others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261170 | |||||||
| chr2:177261170 | C | CAAAA | 8 | a0001c0001t0001g0037 a0001c0001t0001g0193 a0001c0001t0001g0194 others(5): Show |
9 | HG01099.hp2 HG02818.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+3358_45+3361dup others(4): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261170 | |||||||
| chr2:177261179 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.45+3353T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261179 | |||||||
| chr2:177261186 | C | A | 4 | a0001c0001t0001g0174 a0001c0001t0002g0054 a0001c0001t0002g0101 others(1): Show |
5 | HG02257.hp1 HG02486.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+3346G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261186 | |||||||
| chr2:177261187 | A | C | 1 | a0001c0001t0002g0054 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.45+3345T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261187 | |||||||
| chr2:177261224 | C | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.45+3308G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261224 | |||||||
| chr2:177261265 | G | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
8 | HG01361.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+3267C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261265 | |||||||
| chr2:177261366 | G | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.45+3166C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261366 | |||||||
| chr2:177261399 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0035 others(20): Show |
31 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.45+3133G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261399 | |||||||
| chr2:177261588 | C | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0212 a0001c0001t0001g0213 others(1): Show |
8 | HG03831.hp2 NA18939.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+2944G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261588 | |||||||
| chr2:177261818 | G | C | 59 | a0001c0001t0001g0215 a0001c0001t0002g0001 a0001c0001t0002g0006 others(56): Show |
102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.45+2714C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177261818 | |||||||
| chr2:177262312 | A | C | 41 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(38): Show |
54 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.45+2220T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177262312 | |||||||
| chr2:177262361 | A | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0009 others(55): Show |
101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.45+2171T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177262361 | |||||||
| chr2:177262444 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45+2088T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177262444 | |||||||
| chr2:177262739 | AAAT | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
9 | HG01361.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+1790_45+1792del others(3): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177262739 | |||||||
| chr2:177263018 | T | A | 1 | a0001c0001t0002g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.45+1514A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263018 | |||||||
| chr2:177263098 | C | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
9 | HG01361.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+1434G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263098 | |||||||
| chr2:177263111 | T | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0009 others(55): Show |
101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.45+1421A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263111 | |||||||
| chr2:177263275 | T | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(49): Show |
71 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.45+1257A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263275 | |||||||
| chr2:177263405 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.45+1127A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263405 | |||||||
| chr2:177263634 | C | G | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+898G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263634 | |||||||
| chr2:177263720 | C | A | 3 | a0001c0001t0006g0025 a0001c0001t0006g0103 a0001c0001t0006g0104 |
4 | HG02129.hp2 NA18987.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+812G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263720 | |||||||
| chr2:177263763 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+769C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263763 | |||||||
| chr2:177263965 | A | C | 41 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(38): Show |
54 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.45+567T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177263965 | |||||||
| chr2:177264103 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.45+429G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264103 | |||||||
| chr2:177264249 | C | A | 1 | a0001c0001t0001g0218 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.45+283G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264249 | |||||||
| chr2:177264273 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+259C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264273 | |||||||
| chr2:177264276 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+256G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264276 | |||||||
| chr2:177264284 | AGACCTTC others(7): Show |
A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+234_45+247delGT others(12): Show |
NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264284 | |||||||
| chr2:177264299 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+233A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264299 | |||||||
| chr2:177264304 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+228T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264304 | |||||||
| chr2:177264306 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+226G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264306 | |||||||
| chr2:177264328 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+204A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264328 | |||||||
| chr2:177264332 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+200A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264332 | |||||||
| chr2:177264335 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+197C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264335 | |||||||
| chr2:177264357 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+175A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264357 | |||||||
| chr2:177264363 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+169A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264363 | |||||||
| chr2:177264367 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+165G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264367 | |||||||
| chr2:177264375 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+157G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264375 | |||||||
| chr2:177264380 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+152G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264380 | |||||||
| chr2:177264386 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+146G>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264386 | |||||||
| chr2:177264392 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+140C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264392 | |||||||
| chr2:177264394 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+138G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264394 | |||||||
| chr2:177264401 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+131G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264401 | |||||||
| chr2:177264402 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+130T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264402 | |||||||
| chr2:177264407 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+125G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264407 | |||||||
| chr2:177264412 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+120A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264412 | |||||||
| chr2:177264414 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+118G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264414 | |||||||
| chr2:177264415 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+117A>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264415 | |||||||
| chr2:177264419 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+113A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264419 | |||||||
| chr2:177264426 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+106T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264426 | |||||||
| chr2:177264434 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.45+98C>T | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264434 | |||||||
| chr2:177264434 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+98C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264434 | |||||||
| chr2:177264435 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+97C>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264435 | |||||||
| chr2:177264437 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+95T>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264437 | |||||||
| chr2:177264445 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+87A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264445 | |||||||
| chr2:177264453 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+79A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264453 | |||||||
| chr2:177264456 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0002g0048 |
3 | HG01175.hp1 HG04115.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.45+76G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264456 | |||||||
| chr2:177264460 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+72G>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264460 | |||||||
| chr2:177264465 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+67G>A | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264465 | |||||||
| chr2:177264470 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+62A>C | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264470 | |||||||
| chr2:177264475 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+57A>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264475 | |||||||
| chr2:177264476 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.45+56T>G | NFE2L2 | ENSG00000116044.17 | transcript | ENST00000397062.8 | protein_coding | 1/4 | chr2 | 177264476 |