Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4899 |
| ensemblid | ENSG00000106459.15 |
| hgncid | 7996 |
| symbol | NRF1 |
| name | nuclear respiratory factor 1 |
| refseq_nuc | NM_005011.5 |
| refseq_prot | NP_005002.3 |
| ensembl_nuc | ENST00000393232.6 |
| ensembl_prot | ENSP00000376924.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 129611720 |
| end | 129757076 |
| strand | + |
| ver | v1.2 |
| region | chr7:129611720-129757076 |
| region5000 | chr7:129606720-129762076 |
| regionname0 | NRF1_chr7_129611720_129757076 |
| regionname5000 | NRF1_chr7_129606720_129762076 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1509 | 201 | 58 | 30 | 94 | 1 | 17 | NRF1_chr7_129606720_129762076 | NRF1 | ATGGA others(1504): Show |
chr7 | 129606720 | 129762076 | ||
| a0001c0002 | 1/0 | 1509 | 159 | 22 | 39 | 64 | 11 | 22 | NRF1_chr7_129606720_129762076 | NRF1 | ATGGA others(1504): Show |
chr7 | 129606720 | 129762076 | ||
| a0001c0003 | 0/0 | 1509 | 23 | 0 | 3 | 18 | 1 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | ATGGA others(1504): Show |
chr7 | 129606720 | 129762076 | ||
| a0001c0004 | 0/0 | 1509 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | ATGGA others(1504): Show |
chr7 | 129606720 | 129762076 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3516 | 73 | 28 | 13 | 25 | 0 | 7 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0002 | 0/1 | 3514 | 109 | 22 | 14 | 61 | 1 | 10 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3509): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0003 | 0/0 | 3514 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3509): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0004 | 0/0 | 3516 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0006 | 0/0 | 3518 | 2 | 1 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3513): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0007 | 0/0 | 3514 | 6 | 0 | 0 | 6 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3509): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0008 | 0/0 | 3514 | 4 | 4 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3509): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0009 | 0/0 | 3514 | 2 | 2 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3509): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0010 | 0/0 | 3516 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0013 | 0/0 | 3516 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0001t0017 | 0/0 | 3514 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3509): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0001 | 0/0 | 3516 | 34 | 7 | 11 | 7 | 2 | 7 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0002 | 0/0 | 3514 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3509): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0003 | 0/0 | 3514 | 50 | 7 | 13 | 19 | 4 | 7 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3509): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0004 | 0/0 | 3516 | 35 | 1 | 7 | 18 | 3 | 6 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0005 | 0/0 | 3516 | 29 | 3 | 5 | 18 | 1 | 2 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0006 | 1/0 | 3518 | 5 | 2 | 2 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3513): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0011 | 0/0 | 3516 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0012 | 0/0 | 3516 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0014 | 0/0 | 3516 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0015 | 0/0 | 3516 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0002t0016 | 0/0 | 3516 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0003t0001 | 0/0 | 3516 | 23 | 0 | 3 | 18 | 1 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| a0001c0004t0001 | 0/0 | 3516 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | AGAAG others(3511): Show |
chr7 | 129606720 | 129762076 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0013g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0001t0017g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0005g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0006g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0006g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0006g0356 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0006g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0006g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0011g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0012g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0014g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0015g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0002t0016g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0003t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| a0001c0004t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0348 | EUR | GBR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00099 | hp2 | a0001 | c0002 | t0005 | g0330 | EUR | GBR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00140 | hp1 | a0001 | c0002 | t0011 | g0371 | EUR | GBR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0233 | EUR | GBR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0236 | EUR | FIN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00280 | hp2 | a0001 | c0002 | t0004 | g0235 | EUR | FIN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0227 | EUR | FIN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0261 | EUR | FIN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0376 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00423 | hp1 | a0001 | c0002 | t0005 | g0279 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0245 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00597 | hp1 | a0001 | c0002 | t0012 | g0311 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0286 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0229 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0264 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00642 | hp2 | a0001 | c0002 | t0006 | g0380 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0347 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00733 | hp2 | a0001 | c0001 | t0013 | g0121 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG00735 | hp2 | a0001 | c0002 | t0004 | g0260 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0241 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0258 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0316 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0317 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01074 | hp1 | a0001 | c0002 | t0006 | g0381 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0265 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0365 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01167 | hp1 | a0001 | c0002 | t0005 | g0327 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01168 | hp1 | a0001 | c0002 | t0004 | g0257 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01168 | hp2 | a0001 | c0002 | t0004 | g0234 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0228 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0331 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0274 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0359 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0360 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0374 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0370 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01346 | hp2 | a0001 | c0002 | t0005 | g0294 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01433 | hp2 | a0001 | c0002 | t0005 | g0353 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0254 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0332 | EUR | IBS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0238 | EUR | IBS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0277 | EUR | IBS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | IBS | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0284 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0231 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0242 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0382 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01943 | hp2 | a0001 | c0001 | t0017 | g0139 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0243 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0367 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01978 | hp1 | a0001 | c0002 | t0004 | g0256 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01978 | hp2 | a0001 | c0002 | t0005 | g0328 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0372 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01981 | hp2 | a0001 | c0002 | t0005 | g0329 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0237 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02004 | hp1 | a0001 | c0002 | t0004 | g0321 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02027 | hp2 | a0001 | c0002 | t0004 | g0298 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0112 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0352 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0259 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0384 | EAS | KHV | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0135 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0240 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0366 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0355 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0377 | AMR | PEL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0357 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0349 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0383 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02647 | hp1 | a0001 | c0002 | t0005 | g0350 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0110 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0253 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0248 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0282 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0285 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0283 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0340 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0344 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02970 | hp1 | a0001 | c0002 | t0015 | g0351 | AFR | ESN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0138 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0342 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ESN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0341 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0288 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0287 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03654 | hp1 | a0001 | c0002 | t0005 | g0280 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0020 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0361 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0252 | SAS | PJL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03831 | hp1 | a0001 | c0002 | t0004 | g0314 | SAS | BEB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0379 | SAS | BEB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03927 | hp1 | a0001 | c0002 | t0004 | g0335 | SAS | BEB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0313 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0262 | SAS | BEB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04184 | hp2 | a0001 | c0002 | t0004 | g0299 | SAS | BEB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04199 | hp1 | a0001 | c0002 | t0004 | g0302 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04204 | hp2 | a0001 | c0002 | t0004 | g0306 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0239 | SAS | STU | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | YRI | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0247 | EAS | CHB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18612 | hp2 | a0001 | c0002 | t0005 | g0297 | EAS | CHB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18939 | hp1 | a0001 | c0002 | t0005 | g0278 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0290 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0275 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0325 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18947 | hp1 | a0001 | c0002 | t0004 | g0326 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0088 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0074 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18948 | hp2 | a0001 | c0002 | t0005 | g0291 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18949 | hp2 | a0001 | c0002 | t0005 | g0319 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18951 | hp2 | a0001 | c0002 | t0004 | g0323 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0268 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18953 | hp2 | a0001 | c0002 | t0005 | g0333 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0362 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0345 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0271 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0246 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18962 | hp2 | a0001 | c0002 | t0004 | g0318 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18964 | hp1 | a0001 | c0002 | t0005 | g0308 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18965 | hp2 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18968 | hp1 | a0001 | c0002 | t0005 | g0300 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0322 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18970 | hp2 | a0001 | c0002 | t0005 | g0281 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0272 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18972 | hp1 | a0001 | c0002 | t0004 | g0293 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18975 | hp1 | a0001 | c0002 | t0004 | g0230 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18975 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0266 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0270 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0273 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18984 | hp2 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18990 | hp1 | a0001 | c0001 | t0010 | g0216 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18991 | hp2 | a0001 | c0002 | t0004 | g0295 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0249 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18995 | hp2 | a0001 | c0002 | t0004 | g0324 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18998 | hp2 | a0001 | c0002 | t0005 | g0304 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18999 | hp1 | a0001 | c0002 | t0003 | g0276 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19000 | hp1 | a0001 | c0002 | t0004 | g0373 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19006 | hp1 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19006 | hp2 | a0001 | c0002 | t0004 | g0336 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19007 | hp2 | a0001 | c0002 | t0014 | g0378 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19011 | hp1 | a0001 | c0002 | t0005 | g0305 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19030 | hp1 | a0001 | c0002 | t0006 | g0354 | AFR | LWK | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19056 | hp2 | a0001 | c0002 | t0005 | g0309 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19057 | hp2 | a0001 | c0001 | t0007 | g0087 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0255 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19064 | hp2 | a0001 | c0002 | t0005 | g0310 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19065 | hp2 | a0001 | c0002 | t0005 | g0301 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0292 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19070 | hp1 | a0001 | c0002 | t0005 | g0303 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19070 | hp2 | a0001 | c0002 | t0003 | g0250 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19074 | hp1 | a0001 | c0002 | t0005 | g0296 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19075 | hp1 | a0001 | c0002 | t0005 | g0312 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0364 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19078 | hp2 | a0001 | c0002 | t0004 | g0320 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0267 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19080 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19082 | hp2 | a0001 | c0002 | t0004 | g0315 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19083 | hp1 | a0001 | c0002 | t0004 | g0337 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0251 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19087 | hp2 | a0001 | c0002 | t0005 | g0338 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19090 | hp1 | a0001 | c0002 | t0004 | g0307 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ASW | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA20129 | hp2 | a0001 | c0002 | t0016 | g0232 | AFR | ASW | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0369 | EUR | TSI | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0269 | EUR | TSI | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0263 | SAS | GIH | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA20905 | hp2 | a0001 | c0002 | t0005 | g0289 | SAS | GIH | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0334 | AMR | CLM | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0128 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0375 | AFR | ACB | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0025 | AFR | USA | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | USA | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18955 | hp1 | a0001 | c0002 | t0004 | g0346 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0339 | AFR | USA | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | USA | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | LWK | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0117 | REF | REF | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0006 | g0356 | REF | REF | NRF1_chr7_129606720_129762076 | NRF1 | chr7 | 129606720 | 129762076 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:129657492 | T | G | 1 | a0001c0001 | 200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
synonymous_variant | LOW | c.141T>G | p.Ser47Ser | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/11 | 252/3518 | 141/1512 | 47/503 | chr7 | 129657492 | |||
| chr7:129690513 | C | T | 1 | a0001c0003 | 23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
synonymous_variant | LOW | c.573C>T | p.Asp191Asp | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/11 | 684/3518 | 573/1512 | 191/503 | chr7 | 129690513 | |||
| chr7:129709089 | A | C | 1 | a0001c0004 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.621A>C | p.Ala207Ala | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/11 | 732/3518 | 621/1512 | 207/503 | chr7 | 129709089 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:129755235 | G | A | 1 | a0001c0001t0007 | 6 | NA18947.hp2 NA18948.hp1 NA18965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*54G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 54 | chr7 | 129755235 | ||||||
| chr7:129755546 | CAT | C | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(11): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*382_*383delAT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 382 | INFO_REALIGN_3_PRIME | chr7 | 129755546 | |||||
| chr7:129755546 | CATAT | C | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(5): Show |
173 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*380_*383delATAT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 380 | INFO_REALIGN_3_PRIME | chr7 | 129755546 | |||||
| chr7:129755548 | T | C | 1 | a0001c0001t0006 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*367T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 367 | chr7 | 129755548 | ||||||
| chr7:129755652 | G | A | 1 | a0001c0001t0008 | 4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*471G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 471 | chr7 | 129755652 | ||||||
| chr7:129755911 | A | G | 3 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0016 |
37 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*730A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 730 | chr7 | 129755911 | ||||||
| chr7:129756078 | G | A | 1 | a0001c0001t0010 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*897G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 897 | chr7 | 129756078 | ||||||
| chr7:129756137 | C | T | 1 | a0001c0002t0015 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*956C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 956 | chr7 | 129756137 | ||||||
| chr7:129756142 | G | A | 1 | a0001c0001t0008 | 4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*961G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 961 | chr7 | 129756142 | ||||||
| chr7:129756194 | C | A | 1 | a0001c0002t0011 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1013C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 1013 | chr7 | 129756194 | ||||||
| chr7:129756311 | T | C | 1 | a0001c0001t0009 | 2 | HG02145.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1130T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 1130 | chr7 | 129756311 | ||||||
| chr7:129756334 | C | G | 4 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0013 others(1): Show |
56 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1153C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 1153 | chr7 | 129756334 | ||||||
| chr7:129756334 | C | T | 1 | a0001c0002t0014 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1153C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 1153 | chr7 | 129756334 | ||||||
| chr7:129756346 | G | A | 1 | a0001c0001t0017 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1165G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 1165 | chr7 | 129756346 | ||||||
| chr7:129756412 | G | T | 1 | a0001c0002t0011 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1231G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 1231 | chr7 | 129756412 | ||||||
| chr7:129756502 | T | C | 5 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0005 others(2): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1321T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 1321 | chr7 | 129756502 | ||||||
| chr7:129756891 | G | A | 1 | a0001c0002t0016 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1710G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 1710 | chr7 | 129756891 | ||||||
| chr7:129757043 | T | C | 1 | a0001c0002t0012 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1862T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 11/11 | 1862 | chr7 | 129757043 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:129612295 | CGCGGGCG others(1): Show |
C | 342 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(339): Show |
342 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7+484_-7+491delGC others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129612295 | ||||||
| chr7:129612424 | G | A | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-7+600G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129612424 | |||||||
| chr7:129612697 | A | G | 1 | a0001c0001t0001g0343 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-7+873A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129612697 | |||||||
| chr7:129612868 | C | G | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7+1044C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129612868 | |||||||
| chr7:129612885 | T | A | 20 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(17): Show |
20 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.-7+1061T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129612885 | |||||||
| chr7:129613012 | G | A | 116 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(113): Show |
116 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-7+1188G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129613012 | |||||||
| chr7:129613139 | T | C | 1 | a0001c0002t0004g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-7+1315T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129613139 | |||||||
| chr7:129613342 | T | C | 1 | a0001c0002t0001g0345 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-7+1518T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129613342 | |||||||
| chr7:129613528 | G | GT | 7 | a0001c0002t0003g0334 a0001c0002t0004g0335 a0001c0002t0004g0336 others(4): Show |
7 | HG01123.hp2 HG03669.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+1704_-7+1705ins others(1): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129613528 | |||||||
| chr7:129613529 | G | T | 134 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0002g0265 others(131): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-7+1705G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129613529 | |||||||
| chr7:129613579 | C | CA | 6 | a0001c0001t0001g0024 a0001c0001t0002g0021 a0001c0001t0002g0022 others(3): Show |
6 | HG03098.hp1 HG03927.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+1763dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129613579 | ||||||
| chr7:129613709 | G | A | 2 | a0001c0003t0001g0347 a0001c0003t0001g0348 |
2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.-7+1885G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129613709 | |||||||
| chr7:129613758 | G | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-7+1934G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129613758 | |||||||
| chr7:129613800 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7+1976G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129613800 | |||||||
| chr7:129613944 | A | G | 115 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(112): Show |
115 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-7+2120A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129613944 | |||||||
| chr7:129614012 | T | C | 140 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(137): Show |
140 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-7+2188T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614012 | |||||||
| chr7:129614185 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2361G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614185 | |||||||
| chr7:129614215 | A | G | 33 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0225 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.-7+2391A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614215 | |||||||
| chr7:129614375 | G | A | 2 | a0001c0002t0003g0228 a0001c0002t0003g0229 |
2 | HG00639.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-7+2551G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614375 | |||||||
| chr7:129614393 | G | T | 336 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(333): Show |
336 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-7+2569G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614393 | |||||||
| chr7:129614443 | T | TTG | 3 | a0001c0002t0001g0359 a0001c0002t0001g0360 a0001c0002t0001g0384 |
3 | HG01257.hp2 HG01258.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-7+2641_-7+2642dup others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTG | 85 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(82): Show |
85 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-7+2639_-7+2642dup others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTG | 3 | a0001c0001t0007g0108 a0001c0002t0001g0340 a0001c0002t0001g0341 |
3 | HG02886.hp1 HG03453.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.-7+2637_-7+2642dup others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTGT others(1): Show |
5 | a0001c0001t0002g0109 a0001c0001t0008g0110 a0001c0001t0008g0111 others(2): Show |
5 | HG02055.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2635_-7+2642dup others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTGT others(3): Show |
6 | a0001c0002t0001g0342 a0001c0002t0003g0231 a0001c0002t0004g0233 others(3): Show |
6 | HG00140.hp2 HG00280.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+2633_-7+2642dup others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTGT others(5): Show |
51 | a0001c0001t0001g0165 a0001c0002t0002g0265 a0001c0002t0003g0228 others(48): Show |
51 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-7+2631_-7+2642dup others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTGT others(7): Show |
95 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(92): Show |
95 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.-7+2629_-7+2642dup others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTGT others(9): Show |
31 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(28): Show |
31 | HG01070.hp2 HG01071.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.-7+2627_-7+2642dup others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTGT others(11): Show |
29 | a0001c0001t0001g0136 a0001c0001t0001g0159 a0001c0001t0001g0184 others(26): Show |
29 | HG00673.hp2 HG01167.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.-7+2625_-7+2642dup others(18): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTGT others(13): Show |
21 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(18): Show |
21 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7+2623_-7+2642dup others(20): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTGT others(15): Show |
7 | a0001c0001t0001g0144 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG00544.hp2 HG00609.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+2621_-7+2642dup others(22): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614443 | T | TTGTGTGT others(17): Show |
2 | a0001c0001t0001g0163 a0001c0001t0001g0222 |
2 | HG03195.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-7+2642_-7+2643ins others(24): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614443 | ||||||
| chr7:129614482 | ATTTT | A | 113 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0002g0265 others(110): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-7+2666_-7+2669del others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129614482 | ||||||
| chr7:129614517 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-7+2693A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614517 | |||||||
| chr7:129614607 | G | A | 336 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(333): Show |
336 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-7+2783G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614607 | |||||||
| chr7:129614701 | C | G | 1 | a0001c0002t0001g0383 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-7+2877C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614701 | |||||||
| chr7:129614863 | A | G | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-7+3039A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614863 | |||||||
| chr7:129614927 | C | T | 1 | a0001c0002t0004g0235 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-7+3103C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129614927 | |||||||
| chr7:129615072 | C | T | 1 | a0001c0002t0005g0312 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-7+3248C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615072 | |||||||
| chr7:129615074 | G | A | 1 | a0001c0002t0003g0236 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-7+3250G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615074 | |||||||
| chr7:129615146 | T | A | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+3322T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615146 | |||||||
| chr7:129615156 | G | T | 113 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0002g0265 others(110): Show |
113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-7+3332G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615156 | |||||||
| chr7:129615269 | A | T | 202 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(199): Show |
202 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.-7+3445A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615269 | |||||||
| chr7:129615423 | C | CTA | 342 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(339): Show |
342 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7+3600_-7+3601ins others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129615423 | ||||||
| chr7:129615451 | T | G | 1 | a0001c0001t0002g0026 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-7+3627T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615451 | |||||||
| chr7:129615453 | G | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7+3629G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615453 | |||||||
| chr7:129615518 | T | C | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+3694T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615518 | |||||||
| chr7:129615795 | T | G | 1 | a0001c0001t0002g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-7+3971T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615795 | |||||||
| chr7:129615849 | A | T | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7+4025A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129615849 | |||||||
| chr7:129616025 | T | G | 1 | a0001c0002t0005g0328 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-7+4201T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616025 | |||||||
| chr7:129616040 | AAT | A | 3 | a0001c0002t0005g0328 a0001c0002t0005g0329 a0001c0002t0005g0330 |
3 | HG00099.hp2 HG01978.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-7+4228_-7+4229del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129616040 | ||||||
| chr7:129616073 | T | A | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+4249T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616073 | |||||||
| chr7:129616139 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-7+4315G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616139 | |||||||
| chr7:129616435 | A | G | 59 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-7+4611A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616435 | |||||||
| chr7:129616444 | C | T | 174 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(171): Show |
174 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.-7+4620C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616444 | |||||||
| chr7:129616465 | T | C | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-7+4641T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616465 | |||||||
| chr7:129616586 | G | A | 58 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(55): Show |
58 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-7+4762G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616586 | |||||||
| chr7:129616704 | T | G | 1 | a0001c0001t0003g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-7+4880T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616704 | |||||||
| chr7:129616779 | A | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG01891.hp2 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+4955A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616779 | |||||||
| chr7:129616800 | A | G | 1 | a0001c0002t0005g0333 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-7+4976A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129616800 | |||||||
| chr7:129617010 | C | T | 1 | a0001c0002t0012g0311 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-7+5186C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129617010 | |||||||
| chr7:129617043 | T | G | 1 | a0001c0002t0004g0313 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-7+5219T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129617043 | |||||||
| chr7:129617231 | A | T | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+5407A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129617231 | |||||||
| chr7:129617426 | T | C | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+5602T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129617426 | |||||||
| chr7:129617575 | C | T | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-7+5751C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129617575 | |||||||
| chr7:129617587 | T | C | 1 | a0001c0002t0003g0237 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-7+5763T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129617587 | |||||||
| chr7:129617667 | A | G | 115 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(112): Show |
115 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-7+5843A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129617667 | |||||||
| chr7:129617733 | G | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-7+5909G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129617733 | |||||||
| chr7:129617962 | G | A | 3 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 |
3 | HG00558.hp2 NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-7+6138G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129617962 | |||||||
| chr7:129618008 | G | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-7+6184G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618008 | |||||||
| chr7:129618049 | A | G | 1 | a0001c0002t0003g0277 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-7+6225A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618049 | |||||||
| chr7:129618203 | G | A | 1 | a0001c0002t0001g0349 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-7+6379G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618203 | |||||||
| chr7:129618203 | GTGA | G | 48 | a0001c0002t0002g0265 a0001c0002t0003g0228 a0001c0002t0003g0229 others(45): Show |
48 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-7+6388_-7+6390del others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129618203 | ||||||
| chr7:129618300 | G | A | 5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+6476G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618300 | |||||||
| chr7:129618386 | A | G | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+6562A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618386 | |||||||
| chr7:129618419 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-7+6595G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618419 | |||||||
| chr7:129618443 | C | G | 54 | a0001c0002t0002g0265 a0001c0002t0003g0228 a0001c0002t0003g0229 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-7+6619C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618443 | |||||||
| chr7:129618530 | A | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7+6706A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618530 | |||||||
| chr7:129618587 | C | T | 2 | a0001c0002t0003g0275 a0001c0002t0003g0276 |
2 | NA18941.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-7+6763C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618587 | |||||||
| chr7:129618656 | C | G | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7+6832C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618656 | |||||||
| chr7:129618688 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-7+6864C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618688 | |||||||
| chr7:129618758 | A | G | 336 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(333): Show |
336 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-7+6934A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618758 | |||||||
| chr7:129618796 | G | A | 336 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(333): Show |
336 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-7+6972G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618796 | |||||||
| chr7:129618830 | G | A | 223 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(220): Show |
223 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.-7+7006G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129618830 | |||||||
| chr7:129619081 | A | C | 3 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 |
3 | HG00558.hp2 NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-7+7257A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619081 | |||||||
| chr7:129619293 | G | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-7+7469G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619293 | |||||||
| chr7:129619358 | A | G | 48 | a0001c0002t0002g0265 a0001c0002t0003g0228 a0001c0002t0003g0229 others(45): Show |
48 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-7+7534A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619358 | |||||||
| chr7:129619393 | CGT | C | 27 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(24): Show |
27 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.-7+7572_-7+7573del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619393 | ||||||
| chr7:129619394 | GTGTA | G | 64 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(61): Show |
64 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-7+7572_-7+7575del others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619394 | ||||||
| chr7:129619394 | GTGTATA | G | 4 | a0001c0001t0002g0022 a0001c0001t0002g0059 a0001c0001t0002g0070 others(1): Show |
4 | HG01993.hp1 HG02615.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+7572_-7+7577del others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619394 | ||||||
| chr7:129619396 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0002g0046 others(11): Show |
14 | HG00438.hp1 HG01106.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+7572G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619396 | |||||||
| chr7:129619396 | G | GTA | 18 | a0001c0002t0001g0331 a0001c0002t0001g0349 a0001c0002t0002g0265 others(15): Show |
18 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7+7609_-7+7610dup others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | G | GTATA | 18 | a0001c0002t0003g0237 a0001c0002t0003g0266 a0001c0002t0003g0267 others(15): Show |
18 | HG00639.hp1 HG01168.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7+7607_-7+7610dup others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | G | GTATATA | 13 | a0001c0002t0003g0270 a0001c0002t0003g0271 a0001c0002t0003g0272 others(10): Show |
13 | HG00597.hp1 HG01167.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7+7605_-7+7610dup others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | G | GTATATAT others(1): Show |
10 | a0001c0002t0001g0332 a0001c0002t0003g0287 a0001c0002t0004g0307 others(7): Show |
10 | HG00099.hp2 HG01515.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7+7603_-7+7610dup others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | G | GTATATAT others(3): Show |
1 | a0001c0002t0005g0309 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-7+7601_-7+7610dup others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | G | GTATATAT others(5): Show |
3 | a0001c0002t0004g0325 a0001c0002t0004g0326 a0001c0002t0005g0310 |
3 | NA18943.hp2 NA18947.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-7+7599_-7+7610dup others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | G | GTATATAT others(7): Show |
1 | a0001c0002t0003g0274 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-7+7597_-7+7610dup others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | GTA | G | 23 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0191 others(20): Show |
23 | HG00639.hp2 HG00735.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-7+7609_-7+7610del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | GTATA | G | 29 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0190 others(26): Show |
29 | HG00280.hp1 HG00558.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.-7+7607_-7+7610del others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | GTATATA | G | 11 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(8): Show |
11 | HG01069.hp1 HG02257.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7+7605_-7+7610del others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | GTATATAT others(1): Show |
G | 9 | a0001c0001t0001g0165 a0001c0002t0001g0227 a0001c0002t0001g0341 others(6): Show |
9 | HG00323.hp1 HG00642.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+7603_-7+7610del others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | GTATATAT others(3): Show |
G | 29 | a0001c0001t0001g0184 a0001c0002t0001g0164 a0001c0002t0001g0225 others(26): Show |
29 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.-7+7601_-7+7610del others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | GTATATAT others(5): Show |
G | 3 | a0001c0001t0002g0157 a0001c0002t0001g0340 a0001c0002t0001g0361 |
3 | HG01361.hp2 HG02886.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-7+7599_-7+7610del others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619396 | GTATATAT others(9): Show |
G | 2 | a0001c0002t0001g0223 a0001c0002t0001g0224 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-7+7595_-7+7610del others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619396 | ||||||
| chr7:129619400 | A | G | 1 | a0001c0002t0003g0288 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-7+7576A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619400 | |||||||
| chr7:129619402 | A | G | 1 | a0001c0002t0003g0334 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-7+7578A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619402 | |||||||
| chr7:129619419 | TATATATA others(9): Show |
T | 1 | a0001c0002t0005g0289 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-7+7597_-7+7612del others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619419 | ||||||
| chr7:129619421 | TATATATA others(7): Show |
T | 2 | a0001c0001t0001g0358 a0001c0002t0001g0357 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-7+7599_-7+7612del others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619421 | ||||||
| chr7:129619423 | T | C | 14 | a0001c0001t0001g0163 a0001c0001t0001g0178 a0001c0001t0001g0182 others(11): Show |
14 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7+7599T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619423 | |||||||
| chr7:129619423 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01099.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-7+7600_-7+7601ins others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619423 | ||||||
| chr7:129619425 | T | C | 46 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(43): Show |
46 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.-7+7601T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619425 | |||||||
| chr7:129619425 | T | TAC | 11 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(8): Show |
11 | HG00673.hp2 HG01361.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+7602_-7+7603ins others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619425 | ||||||
| chr7:129619425 | T | TACACACA others(1): Show |
4 | a0001c0003t0001g0013 a0001c0003t0001g0014 a0001c0003t0001g0016 others(1): Show |
4 | HG01099.hp1 HG03669.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+7602_-7+7603ins others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619425 | ||||||
| chr7:129619425 | T | TACACACA others(7): Show |
1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-7+7602_-7+7603ins others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619425 | ||||||
| chr7:129619427 | T | C | 97 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(94): Show |
97 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-7+7603T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619427 | |||||||
| chr7:129619427 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-7+7604_-7+7605ins others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619427 | ||||||
| chr7:129619427 | T | TACACACA others(7): Show |
1 | a0001c0003t0001g0002 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-7+7604_-7+7605ins others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619427 | ||||||
| chr7:129619429 | T | C | 198 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(195): Show |
198 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.-7+7605T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619429 | |||||||
| chr7:129619429 | T | TAC | 3 | a0001c0001t0001g0126 a0001c0001t0002g0051 a0001c0001t0002g0052 |
3 | HG00438.hp1 HG01106.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-7+7606_-7+7607ins others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619429 | ||||||
| chr7:129619429 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0159 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7+7606_-7+7607ins others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619429 | ||||||
| chr7:129619431 | T | C | 206 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(203): Show |
206 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.-7+7607T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619431 | |||||||
| chr7:129619431 | T | TACACACA others(3): Show |
1 | a0001c0001t0008g0128 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-7+7608_-7+7609ins others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619431 | ||||||
| chr7:129619431 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-7+7608_-7+7609ins others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619431 | ||||||
| chr7:129619431 | T | TACACACA others(9): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0144 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-7+7608_-7+7609ins others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619431 | ||||||
| chr7:129619433 | T | C | 217 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(214): Show |
217 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.-7+7609T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619433 | |||||||
| chr7:129619433 | T | TACACACA others(9): Show |
1 | a0001c0001t0002g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-7+7624_-7+7625ins others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619433 | ||||||
| chr7:129619433 | T | TATACACA others(13): Show |
1 | a0001c0001t0001g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7+7610_-7+7611ins others(20): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619433 | ||||||
| chr7:129619433 | T | TATATACA others(9): Show |
1 | a0001c0001t0008g0112 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-7+7610_-7+7611ins others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619433 | ||||||
| chr7:129619433 | T | TATATATA others(3): Show |
1 | a0001c0001t0002g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+7610_-7+7611ins others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619433 | ||||||
| chr7:129619435 | C | T | 50 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-7+7611C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619435 | |||||||
| chr7:129619436 | A | ATATATAT others(10): Show |
1 | a0001c0002t0004g0315 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-7+7612_-7+7613ins others(17): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619436 | |||||||
| chr7:129619437 | C | T | 1 | a0001c0002t0004g0302 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-7+7613C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619437 | |||||||
| chr7:129619439 | C | T | 1 | a0001c0002t0004g0302 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-7+7615C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619439 | |||||||
| chr7:129619447 | C | T | 13 | a0001c0001t0001g0182 a0001c0001t0001g0209 a0001c0001t0001g0220 others(10): Show |
13 | HG00544.hp2 HG00609.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+7623C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619447 | |||||||
| chr7:129619449 | T | C | 29 | a0001c0001t0001g0118 a0001c0001t0001g0167 a0001c0001t0001g0193 others(26): Show |
29 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-7+7625T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619449 | |||||||
| chr7:129619451 | T | C | 15 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0004 others(12): Show |
15 | HG00423.hp2 HG00621.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7+7627T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619451 | |||||||
| chr7:129619453 | T | C | 15 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0004 others(12): Show |
15 | HG00423.hp2 HG00621.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7+7629T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619453 | |||||||
| chr7:129619455 | T | C | 25 | a0001c0001t0001g0182 a0001c0001t0001g0209 a0001c0001t0001g0220 others(22): Show |
25 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-7+7631T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619455 | |||||||
| chr7:129619457 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0214 |
2 | HG00597.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-7+7633C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619457 | |||||||
| chr7:129619459 | C | CAT | 12 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(9): Show |
12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+7635_-7+7636ins others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619459 | |||||||
| chr7:129619459 | C | T | 10 | a0001c0001t0001g0182 a0001c0001t0001g0209 a0001c0001t0001g0220 others(7): Show |
10 | HG00544.hp2 HG00609.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+7635C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619459 | |||||||
| chr7:129619459 | CGT | C | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG02083.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+7666_-7+7667del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619459 | ||||||
| chr7:129619459 | CGTGT | C | 7 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0193 others(4): Show |
7 | HG01099.hp2 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+7664_-7+7667del others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619459 | ||||||
| chr7:129619460 | G | A | 130 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(127): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.-7+7636G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619460 | |||||||
| chr7:129619461 | T | C | 9 | a0001c0001t0001g0194 a0001c0001t0001g0214 a0001c0003t0001g0001 others(6): Show |
9 | HG00597.hp2 HG02074.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+7637T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619461 | |||||||
| chr7:129619461 | TGTG | T | 5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+7638_-7+7640del others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619461 | |||||||
| chr7:129619462 | G | A | 23 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(20): Show |
23 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.-7+7638G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619462 | |||||||
| chr7:129619464 | G | A | 22 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0193 others(19): Show |
22 | HG00423.hp2 HG00621.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7+7640G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619464 | |||||||
| chr7:129619466 | G | A | 16 | a0001c0001t0001g0162 a0001c0003t0001g0001 a0001c0003t0001g0003 others(13): Show |
16 | HG00423.hp2 HG00621.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7+7642G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619466 | |||||||
| chr7:129619467 | T | C | 8 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(5): Show |
8 | HG00423.hp2 HG00621.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+7643T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619467 | |||||||
| chr7:129619468 | G | A | 15 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0004 others(12): Show |
15 | HG00423.hp2 HG00621.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7+7644G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619468 | |||||||
| chr7:129619469 | T | C | 15 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0004 others(12): Show |
15 | HG00423.hp2 HG00621.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7+7645T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619469 | |||||||
| chr7:129619470 | G | A | 15 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0004 others(12): Show |
15 | HG00423.hp2 HG00621.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7+7646G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619470 | |||||||
| chr7:129619471 | T | C | 7 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0004 others(4): Show |
7 | HG02074.hp2 NA18940.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+7647T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619471 | |||||||
| chr7:129619472 | G | A | 7 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0004 others(4): Show |
7 | HG02074.hp2 NA18940.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+7648G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619472 | |||||||
| chr7:129619478 | GTGTGTGT others(9): Show |
G | 3 | a0001c0001t0002g0030 a0001c0001t0002g0060 a0001c0001t0002g0061 |
3 | NA18945.hp1 NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-7+7656_-7+7671del others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619478 | ||||||
| chr7:129619478 | GTGTGTGT others(19): Show |
G | 6 | a0001c0003t0001g0002 a0001c0003t0001g0013 a0001c0003t0001g0014 others(3): Show |
6 | HG01099.hp1 HG01109.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+7656_-7+7681del others(26): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619478 | ||||||
| chr7:129619482 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7+7658G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619482 | |||||||
| chr7:129619482 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0002g0026 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-7+7660_-7+7673del others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619482 | ||||||
| chr7:129619484 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0002t0001g0363 |
3 | HG02258.hp2 HG03209.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-7+7660G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619484 | |||||||
| chr7:129619484 | GTGTGTGT others(1): Show |
G | 7 | a0001c0002t0003g0277 a0001c0002t0003g0282 a0001c0002t0003g0283 others(4): Show |
7 | HG00639.hp1 HG01516.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+7662_-7+7669del others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619484 | ||||||
| chr7:129619484 | GTGTGTGT others(3): Show |
G | 45 | a0001c0001t0007g0108 a0001c0002t0002g0265 a0001c0002t0003g0228 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-7+7662_-7+7671del others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619484 | ||||||
| chr7:129619486 | G | A | 25 | a0001c0001t0001g0165 a0001c0001t0001g0170 a0001c0001t0001g0171 others(22): Show |
25 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-7+7662G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619486 | |||||||
| chr7:129619486 | G | GTA | 13 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0359 others(10): Show |
13 | HG00408.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+7663_-7+7664ins others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619486 | ||||||
| chr7:129619486 | G | GTATA | 24 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0176 others(21): Show |
24 | HG00642.hp2 HG01074.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-7+7663_-7+7664ins others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619486 | ||||||
| chr7:129619486 | G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0178 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7+7663_-7+7664ins others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619486 | ||||||
| chr7:129619486 | GTGTGTA | G | 14 | a0001c0001t0001g0024 a0001c0001t0001g0136 a0001c0001t0002g0021 others(11): Show |
14 | HG02083.hp2 HG02970.hp1 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7+7664_-7+7669del others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619486 | ||||||
| chr7:129619486 | GTGTGTAT others(1): Show |
G | 5 | a0001c0001t0002g0051 a0001c0001t0002g0054 a0001c0001t0002g0119 others(2): Show |
5 | HG00735.hp1 HG01074.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+7664_-7+7671del others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619486 | ||||||
| chr7:129619486 | GTGTGTAT others(3): Show |
G | 1 | a0001c0002t0003g0238 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-7+7664_-7+7673del others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619486 | ||||||
| chr7:129619488 | G | A | 80 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(77): Show |
80 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-7+7664G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619488 | |||||||
| chr7:129619488 | G | GTATA | 6 | a0001c0001t0001g0198 a0001c0001t0001g0215 a0001c0001t0001g0219 others(3): Show |
6 | HG02135.hp2 HG02630.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+7665_-7+7666ins others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619488 | ||||||
| chr7:129619488 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0184 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-7+7665_-7+7666ins others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619488 | ||||||
| chr7:129619488 | G | GTATATAT others(7): Show |
1 | a0001c0001t0001g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-7+7665_-7+7666ins others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619488 | ||||||
| chr7:129619488 | GTGTA | G | 7 | a0001c0001t0001g0078 a0001c0001t0001g0118 a0001c0001t0001g0123 others(4): Show |
7 | HG01167.hp2 HG02257.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+7666_-7+7669del others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619488 | ||||||
| chr7:129619488 | GTGTATA | G | 71 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0126 others(68): Show |
71 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-7+7666_-7+7671del others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619488 | ||||||
| chr7:129619488 | GTGTATAT others(1): Show |
G | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0013g0121 others(1): Show |
4 | HG00733.hp2 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+7666_-7+7673del others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619488 | ||||||
| chr7:129619488 | GTGTATAT others(9): Show |
G | 8 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(5): Show |
8 | HG00423.hp2 HG00621.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+7666_-7+7681del others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619488 | ||||||
| chr7:129619490 | G | A | 92 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-7+7666G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619490 | |||||||
| chr7:129619490 | G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG02135.hp1 NA18965.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+7682_-7+7689dup others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-7+7680_-7+7689dup others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | G | GTGTATAT others(3): Show |
1 | a0001c0001t0002g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7+7667_-7+7668ins others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | G | GTGTATAT others(5): Show |
1 | a0001c0001t0002g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-7+7667_-7+7668ins others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | G | GTGTGTAT others(3): Show |
1 | a0001c0001t0002g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-7+7667_-7+7668ins others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0002g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7+7667_-7+7668ins others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0002g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-7+7667_-7+7668ins others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0002g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7+7667_-7+7668ins others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | GTA | G | 3 | a0001c0001t0008g0110 a0001c0001t0008g0112 a0001c0002t0005g0350 |
3 | HG02055.hp1 HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-7+7688_-7+7689del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | GTATA | G | 6 | a0001c0001t0002g0052 a0001c0001t0002g0107 a0001c0001t0007g0095 others(3): Show |
6 | HG00438.hp1 HG02886.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+7686_-7+7689del others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | GTATATA | G | 12 | a0001c0001t0002g0023 a0001c0001t0002g0034 a0001c0001t0002g0053 others(9): Show |
12 | HG01433.hp2 HG04115.hp2 HG04184.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+7684_-7+7689del others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | GTATATAT others(1): Show |
G | 45 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(42): Show |
45 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.-7+7682_-7+7689del others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | GTATATAT others(3): Show |
G | 9 | a0001c0002t0004g0295 a0001c0002t0004g0307 a0001c0002t0004g0314 others(6): Show |
9 | HG00423.hp1 HG01346.hp2 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+7680_-7+7689del others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619490 | GTATATAT others(7): Show |
G | 7 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0004 others(4): Show |
7 | HG02074.hp2 NA18940.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+7676_-7+7689del others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619490 | ||||||
| chr7:129619492 | A | G | 7 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(4): Show |
7 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+7668A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619492 | |||||||
| chr7:129619494 | A | G | 6 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(3): Show |
6 | HG01361.hp2 HG02647.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+7670A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619494 | |||||||
| chr7:129619496 | A | G | 4 | a0001c0001t0002g0052 a0001c0002t0001g0340 a0001c0002t0001g0341 others(1): Show |
4 | HG00438.hp1 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+7672A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619496 | |||||||
| chr7:129619498 | A | G | 6 | a0001c0002t0001g0341 a0001c0002t0004g0299 a0001c0002t0004g0306 others(3): Show |
6 | HG03453.hp1 HG04184.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+7674A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619498 | |||||||
| chr7:129619500 | A | G | 50 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.-7+7676A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619500 | |||||||
| chr7:129619502 | A | G | 3 | a0001c0002t0003g0290 a0001c0002t0004g0321 a0001c0002t0005g0300 |
3 | HG02004.hp1 NA18939.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-7+7678A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619502 | |||||||
| chr7:129619736 | G | GT | 186 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(183): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-7+7927dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129619736 | ||||||
| chr7:129619736 | G | T | 1 | a0001c0001t0001g0219 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-7+7912G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619736 | |||||||
| chr7:129619902 | C | T | 84 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(81): Show |
84 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.-7+8078C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619902 | |||||||
| chr7:129619951 | T | A | 223 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(220): Show |
223 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.-7+8127T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129619951 | |||||||
| chr7:129620369 | G | A | 58 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(55): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.-7+8545G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620369 | |||||||
| chr7:129620388 | CT | C | 202 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(199): Show |
202 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.-7+8582delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129620388 | ||||||
| chr7:129620394 | T | C | 2 | a0001c0003t0001g0347 a0001c0003t0001g0348 |
2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.-7+8570T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620394 | |||||||
| chr7:129620480 | C | A | 1 | a0001c0001t0002g0031 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-7+8656C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620480 | |||||||
| chr7:129620666 | A | G | 339 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(336): Show |
339 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.-7+8842A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620666 | |||||||
| chr7:129620677 | C | A | 20 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(17): Show |
20 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.-7+8853C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620677 | |||||||
| chr7:129620693 | C | T | 115 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0331 others(112): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-7+8869C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620693 | |||||||
| chr7:129620695 | A | G | 3 | a0001c0002t0001g0349 a0001c0002t0005g0350 a0001c0002t0005g0353 |
3 | HG01433.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-7+8871A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620695 | |||||||
| chr7:129620729 | A | G | 1 | a0001c0002t0002g0265 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-7+8905A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620729 | |||||||
| chr7:129620762 | T | A | 2 | a0001c0002t0005g0280 a0001c0002t0005g0327 |
2 | HG01167.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-7+8938T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620762 | |||||||
| chr7:129620775 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-7+8951G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620775 | |||||||
| chr7:129620962 | C | T | 22 | a0001c0001t0002g0058 a0001c0003t0001g0001 a0001c0003t0001g0002 others(19): Show |
22 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7+9138C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129620962 | |||||||
| chr7:129621254 | A | G | 22 | a0001c0001t0002g0058 a0001c0003t0001g0001 a0001c0003t0001g0002 others(19): Show |
22 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7+9430A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129621254 | |||||||
| chr7:129621274 | G | A | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+9450G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129621274 | |||||||
| chr7:129621678 | A | G | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | NA18945.hp2 NA18963.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+9854A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129621678 | |||||||
| chr7:129621781 | AT | A | 211 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(208): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.-7+9976delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129621781 | ||||||
| chr7:129621781 | ATT | A | 23 | a0001c0001t0002g0033 a0001c0001t0002g0046 a0001c0001t0002g0058 others(20): Show |
23 | HG00423.hp2 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-7+9975_-7+9976del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129621781 | ||||||
| chr7:129621825 | C | T | 7 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(4): Show |
7 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7+10001C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129621825 | |||||||
| chr7:129621921 | T | C | 5 | a0001c0001t0001g0165 a0001c0001t0001g0214 a0001c0001t0001g0217 others(2): Show |
5 | HG00597.hp2 HG00621.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+10097T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129621921 | |||||||
| chr7:129621938 | A | G | 5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+10114A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129621938 | |||||||
| chr7:129621944 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-7+10120G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129621944 | |||||||
| chr7:129621974 | G | A | 1 | a0001c0002t0003g0242 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-7+10150G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129621974 | |||||||
| chr7:129622011 | G | A | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+10187G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622011 | |||||||
| chr7:129622081 | G | A | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+10257G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622081 | |||||||
| chr7:129622220 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-7+10396A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622220 | |||||||
| chr7:129622226 | G | A | 22 | a0001c0001t0001g0165 a0001c0001t0001g0175 a0001c0001t0001g0176 others(19): Show |
22 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7+10402G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622226 | |||||||
| chr7:129622317 | A | G | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+10493A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622317 | |||||||
| chr7:129622318 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-7+10494T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622318 | |||||||
| chr7:129622418 | T | C | 336 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(333): Show |
336 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-7+10594T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622418 | |||||||
| chr7:129622524 | A | T | 10 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(7): Show |
10 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7+10700A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622524 | |||||||
| chr7:129622557 | CTTTCT | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7+10747_-7+10751d others(7): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129622557 | ||||||
| chr7:129622561 | C | G | 8 | a0001c0002t0004g0315 a0001c0002t0004g0318 a0001c0002t0004g0320 others(5): Show |
8 | NA18943.hp2 NA18947.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+10737C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622561 | |||||||
| chr7:129622571 | C | CT | 28 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(25): Show |
28 | HG00544.hp1 HG00609.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+10763dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129622571 | ||||||
| chr7:129622571 | CT | C | 104 | a0001c0001t0002g0059 a0001c0002t0001g0331 a0001c0002t0001g0332 others(101): Show |
104 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-7+10763delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129622571 | ||||||
| chr7:129622655 | T | C | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+10831T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622655 | |||||||
| chr7:129622911 | C | T | 2 | a0001c0001t0002g0101 a0001c0001t0002g0102 |
2 | HG02056.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-7+11087C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622911 | |||||||
| chr7:129622983 | A | G | 9 | a0001c0002t0005g0297 a0001c0002t0005g0300 a0001c0002t0005g0301 others(6): Show |
9 | NA18612.hp2 NA18949.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+11159A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129622983 | |||||||
| chr7:129623022 | A | G | 1 | a0001c0003t0001g0012 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-7+11198A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623022 | |||||||
| chr7:129623228 | C | A | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+11404C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623228 | |||||||
| chr7:129623380 | GT | G | 253 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-7+11569delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129623380 | ||||||
| chr7:129623380 | GTT | G | 113 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(110): Show |
113 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-7+11568_-7+11569d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129623380 | ||||||
| chr7:129623386 | T | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-7+11562T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623386 | |||||||
| chr7:129623394 | G | A | 10 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
10 | HG02083.hp2 NA18946.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7+11570G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623394 | |||||||
| chr7:129623490 | A | T | 1 | a0001c0002t0001g0379 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-7+11666A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623490 | |||||||
| chr7:129623491 | T | C | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+11667T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623491 | |||||||
| chr7:129623529 | C | G | 4 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(1): Show |
4 | HG01261.hp2 HG01433.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+11705C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623529 | |||||||
| chr7:129623556 | A | T | 219 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(216): Show |
219 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.-7+11732A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623556 | |||||||
| chr7:129623706 | T | G | 1 | a0001c0001t0002g0073 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-7+11882T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623706 | |||||||
| chr7:129623719 | A | G | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+11895A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623719 | |||||||
| chr7:129623793 | C | T | 1 | a0001c0002t0003g0334 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-7+11969C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623793 | |||||||
| chr7:129623973 | G | T | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+12149G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129623973 | |||||||
| chr7:129624190 | A | G | 73 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(70): Show |
73 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-7+12366A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129624190 | |||||||
| chr7:129624335 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-7+12511G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129624335 | |||||||
| chr7:129624365 | A | C | 4 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0225 others(1): Show |
4 | HG03491.hp2 HG03492.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+12541A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129624365 | |||||||
| chr7:129624491 | G | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+12667G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129624491 | |||||||
| chr7:129624673 | G | T | 1 | a0001c0001t0002g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-7+12849G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129624673 | |||||||
| chr7:129624729 | G | C | 54 | a0001c0002t0002g0265 a0001c0002t0003g0228 a0001c0002t0003g0229 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-7+12905G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129624729 | |||||||
| chr7:129625302 | C | T | 63 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(60): Show |
63 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-7+13478C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625302 | |||||||
| chr7:129625314 | G | A | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+13490G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625314 | |||||||
| chr7:129625443 | G | C | 1 | a0001c0002t0001g0227 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-7+13619G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625443 | |||||||
| chr7:129625450 | A | T | 1 | a0001c0001t0002g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-7+13626A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625450 | |||||||
| chr7:129625527 | G | A | 1 | a0001c0002t0004g0302 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-7+13703G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625527 | |||||||
| chr7:129625653 | A | C | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+13829A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625653 | |||||||
| chr7:129625675 | A | AT | 280 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0118 others(277): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-7+13875dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129625675 | ||||||
| chr7:129625675 | A | ATT | 44 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0136 others(41): Show |
44 | HG00621.hp2 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.-7+13874_-7+13875d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129625675 | ||||||
| chr7:129625675 | A | ATTTT | 14 | a0001c0003t0001g0002 a0001c0003t0001g0005 a0001c0003t0001g0008 others(11): Show |
14 | HG01099.hp1 HG01109.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+13872_-7+13875d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129625675 | ||||||
| chr7:129625675 | ATTTTTT | A | 9 | a0001c0001t0001g0126 a0001c0001t0002g0109 a0001c0001t0002g0119 others(6): Show |
9 | HG00733.hp2 HG00735.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+13870_-7+13875d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129625675 | ||||||
| chr7:129625705 | G | A | 61 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(58): Show |
61 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.-7+13881G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625705 | |||||||
| chr7:129625745 | G | A | 2 | a0001c0001t0002g0131 a0001c0001t0009g0135 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-7+13921G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625745 | |||||||
| chr7:129625798 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-7+13974C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625798 | |||||||
| chr7:129625823 | G | A | 1 | a0001c0002t0001g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-7+13999G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625823 | |||||||
| chr7:129625830 | T | C | 1 | a0001c0001t0006g0211 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-7+14006T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625830 | |||||||
| chr7:129625839 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0002t0003g0352 |
3 | HG01099.hp2 HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-7+14015A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625839 | |||||||
| chr7:129625884 | A | G | 5 | a0001c0001t0002g0023 a0001c0002t0005g0301 a0001c0002t0005g0308 others(2): Show |
5 | HG01978.hp2 HG04115.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+14060A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625884 | |||||||
| chr7:129625959 | A | G | 212 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(209): Show |
212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.-7+14135A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625959 | |||||||
| chr7:129625972 | A | G | 5 | a0001c0002t0003g0282 a0001c0002t0003g0284 a0001c0002t0003g0285 others(2): Show |
5 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+14148A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129625972 | |||||||
| chr7:129626148 | A | G | 3 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 |
3 | HG02055.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-7+14324A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129626148 | |||||||
| chr7:129626536 | A | G | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+14712A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129626536 | |||||||
| chr7:129626576 | T | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(112): Show |
115 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-7+14752T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129626576 | |||||||
| chr7:129626650 | T | C | 73 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(70): Show |
73 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-7+14826T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129626650 | |||||||
| chr7:129626755 | TCTC | T | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+14934_-7+14936d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129626755 | ||||||
| chr7:129626822 | T | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7+14998T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129626822 | |||||||
| chr7:129626911 | A | G | 1 | a0001c0002t0003g0254 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-7+15087A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129626911 | |||||||
| chr7:129626918 | G | T | 336 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(333): Show |
336 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-7+15094G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129626918 | |||||||
| chr7:129627266 | A | G | 59 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-7+15442A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129627266 | |||||||
| chr7:129627311 | A | G | 54 | a0001c0002t0002g0265 a0001c0002t0003g0228 a0001c0002t0003g0229 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-7+15487A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129627311 | |||||||
| chr7:129627323 | C | A | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+15499C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129627323 | |||||||
| chr7:129627329 | A | C | 110 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-7+15505A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129627329 | |||||||
| chr7:129627364 | A | G | 2 | a0001c0002t0001g0359 a0001c0002t0001g0360 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-7+15540A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129627364 | |||||||
| chr7:129627402 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-7+15578G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129627402 | |||||||
| chr7:129627436 | G | T | 110 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-7+15612G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129627436 | |||||||
| chr7:129627460 | A | G | 2 | a0001c0001t0002g0130 a0001c0001t0002g0134 |
2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-7+15636A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129627460 | |||||||
| chr7:129627794 | A | G | 342 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(339): Show |
342 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7+15970A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129627794 | |||||||
| chr7:129628030 | GGTTCTTT others(62): Show |
G | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-7+16209_-7+16277d others(71): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129628030 | ||||||
| chr7:129628034 | C | CT | 13 | a0001c0002t0001g0364 a0001c0002t0001g0366 a0001c0002t0001g0367 others(10): Show |
13 | HG01934.hp2 HG01975.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7+16237dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129628034 | ||||||
| chr7:129628034 | CT | C | 12 | a0001c0002t0004g0230 a0001c0002t0004g0233 a0001c0002t0004g0295 others(9): Show |
12 | HG00140.hp2 HG01981.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+16237delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129628034 | ||||||
| chr7:129628034 | CTT | C | 45 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0242 others(42): Show |
45 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.-7+16236_-7+16237d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129628034 | ||||||
| chr7:129628034 | CTTT | C | 79 | a0001c0001t0001g0214 a0001c0001t0002g0022 a0001c0001t0002g0023 others(76): Show |
79 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-7+16235_-7+16237d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129628034 | ||||||
| chr7:129628034 | CTTTT | C | 115 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0118 others(112): Show |
115 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-7+16234_-7+16237d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129628034 | ||||||
| chr7:129628034 | CTTTTT | C | 56 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0172 others(53): Show |
56 | HG00544.hp2 HG00609.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.-7+16233_-7+16237d others(7): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129628034 | ||||||
| chr7:129628034 | CTTTTTT | C | 11 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(8): Show |
11 | HG01069.hp2 HG01071.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+16232_-7+16237d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129628034 | ||||||
| chr7:129628034 | CTTTTTTT others(10): Show |
C | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+16221_-7+16237d others(19): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129628034 | ||||||
| chr7:129628104 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-7+16280C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628104 | |||||||
| chr7:129628105 | A | G | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+16281A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628105 | |||||||
| chr7:129628168 | C | T | 1 | a0001c0001t0009g0135 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-7+16344C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628168 | |||||||
| chr7:129628188 | T | C | 220 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(217): Show |
220 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.-7+16364T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628188 | |||||||
| chr7:129628306 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-7+16482A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628306 | |||||||
| chr7:129628322 | A | G | 1 | a0001c0002t0003g0282 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-7+16498A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628322 | |||||||
| chr7:129628430 | A | C | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+16606A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628430 | |||||||
| chr7:129628444 | A | T | 11 | a0001c0001t0001g0184 a0001c0001t0001g0198 a0001c0001t0001g0199 others(8): Show |
11 | HG00673.hp2 HG01361.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+16620A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628444 | |||||||
| chr7:129628454 | C | T | 54 | a0001c0002t0002g0265 a0001c0002t0003g0228 a0001c0002t0003g0229 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-7+16630C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628454 | |||||||
| chr7:129628779 | G | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-7+16955G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129628779 | |||||||
| chr7:129629254 | C | T | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+17430C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129629254 | |||||||
| chr7:129629277 | C | CT | 60 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-7+17468dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129629277 | ||||||
| chr7:129629292 | T | C | 1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-7+17468T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129629292 | |||||||
| chr7:129629316 | T | G | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-7+17492T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129629316 | |||||||
| chr7:129629385 | T | C | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+17561T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129629385 | |||||||
| chr7:129629512 | T | G | 1 | a0001c0002t0004g0292 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-7+17688T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129629512 | |||||||
| chr7:129629613 | G | A | 59 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-7+17789G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129629613 | |||||||
| chr7:129629921 | A | G | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7+18097A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129629921 | |||||||
| chr7:129629922 | G | T | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+18098G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129629922 | |||||||
| chr7:129629995 | C | A | 62 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(59): Show |
62 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-7+18171C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129629995 | |||||||
| chr7:129630311 | G | A | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+18487G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129630311 | |||||||
| chr7:129630368 | T | C | 380 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(377): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.-7+18544T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129630368 | |||||||
| chr7:129630469 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-7+18645A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129630469 | |||||||
| chr7:129630797 | A | G | 5 | a0001c0002t0003g0237 a0001c0002t0003g0258 a0001c0002t0003g0262 others(2): Show |
5 | HG00642.hp1 HG01070.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+18973A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129630797 | |||||||
| chr7:129630862 | G | A | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+19038G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129630862 | |||||||
| chr7:129630928 | C | T | 11 | a0001c0002t0004g0293 a0001c0002t0004g0307 a0001c0002t0004g0315 others(8): Show |
11 | NA18943.hp2 NA18947.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7+19104C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129630928 | |||||||
| chr7:129630938 | C | T | 1 | a0001c0002t0003g0255 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-7+19114C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129630938 | |||||||
| chr7:129631236 | AT | A | 207 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(204): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.-7+19427delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129631236 | ||||||
| chr7:129631236 | ATT | A | 112 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(109): Show |
112 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.-7+19426_-7+19427d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129631236 | ||||||
| chr7:129631236 | ATTT | A | 10 | a0001c0001t0001g0126 a0001c0001t0002g0048 a0001c0001t0002g0058 others(7): Show |
10 | HG00733.hp2 HG00735.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+19425_-7+19427d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129631236 | ||||||
| chr7:129631599 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG01891.hp2 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+19775G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129631599 | |||||||
| chr7:129631685 | C | G | 1 | a0001c0001t0002g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-7+19861C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129631685 | |||||||
| chr7:129631725 | A | G | 73 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(70): Show |
73 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-7+19901A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129631725 | |||||||
| chr7:129631780 | TAA | T | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+19957_-7+19958d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129631780 | |||||||
| chr7:129632017 | G | A | 40 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(37): Show |
40 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.-7+20193G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129632017 | |||||||
| chr7:129632158 | C | T | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+20334C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129632158 | |||||||
| chr7:129632251 | A | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | NA18940.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-7+20427A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129632251 | |||||||
| chr7:129632498 | A | G | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+20674A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129632498 | |||||||
| chr7:129632518 | G | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(112): Show |
115 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-7+20694G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129632518 | |||||||
| chr7:129632639 | A | G | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-7+20815A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129632639 | |||||||
| chr7:129632673 | TAA | T | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+20853_-7+20854d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129632673 | ||||||
| chr7:129632776 | T | C | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+20952T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129632776 | |||||||
| chr7:129632848 | A | T | 5 | a0001c0002t0003g0283 a0001c0002t0003g0284 a0001c0002t0003g0285 others(2): Show |
5 | HG00639.hp1 HG01891.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+21024A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129632848 | |||||||
| chr7:129632898 | T | C | 1 | a0001c0002t0005g0281 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-7+21074T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129632898 | |||||||
| chr7:129633002 | AG | A | 54 | a0001c0002t0002g0265 a0001c0002t0003g0228 a0001c0002t0003g0229 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-7+21179delG | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129633002 | |||||||
| chr7:129633575 | A | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+21751A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129633575 | |||||||
| chr7:129633788 | A | ATG | 113 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(110): Show |
113 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.-7+21978_-7+21979d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129633788 | ||||||
| chr7:129633788 | ATG | A | 122 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(119): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-7+21978_-7+21979d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129633788 | ||||||
| chr7:129633804 | A | G | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0133 |
3 | HG02615.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-7+21980A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129633804 | |||||||
| chr7:129634001 | G | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(112): Show |
115 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-7+22177G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634001 | |||||||
| chr7:129634029 | T | TA | 60 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0118 others(57): Show |
60 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-7+22218dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634029 | ||||||
| chr7:129634029 | TA | T | 9 | a0001c0001t0001g0209 a0001c0001t0002g0145 a0001c0002t0001g0357 others(6): Show |
9 | HG02451.hp1 HG02602.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+22218delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634029 | ||||||
| chr7:129634029 | TAA | T | 7 | a0001c0002t0003g0236 a0001c0002t0003g0238 a0001c0002t0003g0253 others(4): Show |
7 | HG00280.hp1 HG01257.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+22217_-7+22218d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634029 | ||||||
| chr7:129634037 | A | AT | 12 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0186 others(9): Show |
12 | HG02970.hp2 NA18942.hp1 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+22213_-7+22214i others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634037 | |||||||
| chr7:129634037 | A | T | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-7+22213A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634037 | |||||||
| chr7:129634039 | A | AT | 15 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0192 others(12): Show |
15 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7+22215_-7+22216i others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634039 | |||||||
| chr7:129634039 | A | ATAT | 4 | a0001c0001t0001g0165 a0001c0001t0001g0193 a0001c0001t0001g0197 others(1): Show |
4 | HG02083.hp1 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+22215_-7+22216i others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634039 | |||||||
| chr7:129634039 | A | T | 28 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0186 others(25): Show |
28 | HG00642.hp2 HG00673.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7+22215A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634039 | |||||||
| chr7:129634039 | AAAAGATA others(3): Show |
A | 1 | a0001c0002t0001g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-7+22217_-7+22226d others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634039 | ||||||
| chr7:129634040 | AAAG | A | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(8): Show |
11 | HG01516.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7+22218_-7+22220d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634040 | ||||||
| chr7:129634041 | A | AT | 5 | a0001c0001t0001g0136 a0001c0001t0001g0206 a0001c0001t0002g0090 others(2): Show |
5 | HG02145.hp2 HG02698.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+22217_-7+22218i others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634041 | |||||||
| chr7:129634041 | A | ATAT | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+22217_-7+22218i others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634041 | |||||||
| chr7:129634041 | A | T | 62 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0001t0001g0174 others(59): Show |
62 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-7+22217A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634041 | |||||||
| chr7:129634041 | AAG | A | 38 | a0001c0001t0017g0139 a0001c0002t0002g0265 a0001c0002t0003g0228 others(35): Show |
38 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-7+22219_-7+22220d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634041 | ||||||
| chr7:129634042 | AG | A | 41 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0167 others(38): Show |
41 | HG00280.hp2 HG00609.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.-7+22219delG | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634042 | |||||||
| chr7:129634042 | AGAT | A | 13 | a0001c0002t0003g0258 a0001c0003t0001g0001 a0001c0003t0001g0002 others(10): Show |
13 | HG00423.hp2 HG00621.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7+22219_-7+22221d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634042 | |||||||
| chr7:129634043 | G | A | 137 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0118 others(134): Show |
137 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-7+22219G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634043 | |||||||
| chr7:129634043 | G | T | 133 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0161 others(130): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-7+22219G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634043 | |||||||
| chr7:129634044 | A | ATTT | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+22221_-7+22222i others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634044 | ||||||
| chr7:129634044 | A | T | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-7+22220A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634044 | |||||||
| chr7:129634045 | T | A | 18 | a0001c0001t0002g0054 a0001c0002t0003g0237 a0001c0002t0003g0243 others(15): Show |
18 | HG00642.hp1 HG01346.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.-7+22221T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634045 | |||||||
| chr7:129634046 | A | T | 3 | a0001c0001t0001g0159 a0001c0001t0002g0156 a0001c0001t0006g0160 |
3 | HG02896.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-7+22222A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634046 | |||||||
| chr7:129634047 | T | A | 1 | a0001c0003t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-7+22223T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634047 | |||||||
| chr7:129634052 | A | C | 1 | a0001c0002t0002g0265 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-7+22228A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634052 | |||||||
| chr7:129634057 | T | C | 5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+22233T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634057 | |||||||
| chr7:129634059 | T | C | 11 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0214 others(8): Show |
11 | HG00597.hp2 HG01361.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+22235T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634059 | |||||||
| chr7:129634059 | T | TACAC | 3 | a0001c0001t0002g0130 a0001c0001t0002g0134 a0001c0001t0009g0135 |
3 | HG01243.hp1 HG01516.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-7+22236_-7+22237i others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634059 | ||||||
| chr7:129634059 | T | TACACAC | 60 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0118 others(57): Show |
60 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-7+22236_-7+22237i others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634059 | ||||||
| chr7:129634059 | T | TACACACA others(1): Show |
11 | a0001c0001t0002g0023 a0001c0001t0002g0031 a0001c0001t0002g0059 others(8): Show |
11 | HG00673.hp1 HG01074.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+22236_-7+22237i others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634059 | ||||||
| chr7:129634059 | T | TACACACA others(3): Show |
2 | a0001c0001t0002g0022 a0001c0001t0008g0128 |
2 | HG02486.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-7+22236_-7+22237i others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634059 | ||||||
| chr7:129634061 | T | C | 127 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0118 others(124): Show |
127 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.-7+22237T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634061 | |||||||
| chr7:129634061 | T | TACACACA others(1): Show |
35 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0126 others(32): Show |
35 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.-7+22254_-7+22261d others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634061 | ||||||
| chr7:129634061 | TACACAC | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 |
3 | HG02630.hp2 HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-7+22256_-7+22261d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634061 | ||||||
| chr7:129634061 | TACACACA others(1): Show |
T | 5 | a0001c0001t0001g0172 a0001c0001t0001g0178 a0001c0001t0001g0180 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+22254_-7+22261d others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634061 | ||||||
| chr7:129634061 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0167 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-7+22252_-7+22261d others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129634061 | ||||||
| chr7:129634063 | C | T | 92 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(89): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-7+22239C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634063 | |||||||
| chr7:129634067 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-7+22243C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634067 | |||||||
| chr7:129634069 | C | T | 5 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+22245C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634069 | |||||||
| chr7:129634071 | C | T | 10 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0170 others(7): Show |
10 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7+22247C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634071 | |||||||
| chr7:129634131 | G | A | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+22307G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634131 | |||||||
| chr7:129634164 | A | G | 328 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(325): Show |
328 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-7+22340A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634164 | |||||||
| chr7:129634180 | T | C | 1 | a0001c0002t0003g0277 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-7+22356T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634180 | |||||||
| chr7:129634259 | C | G | 3 | a0001c0002t0001g0362 a0001c0002t0001g0376 a0001c0002t0014g0378 |
3 | HG00408.hp2 NA18954.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-7+22435C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634259 | |||||||
| chr7:129634329 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-7+22505G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634329 | |||||||
| chr7:129634421 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-7+22597C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634421 | |||||||
| chr7:129634424 | A | G | 110 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-7+22600A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634424 | |||||||
| chr7:129634636 | A | G | 1 | a0001c0002t0005g0297 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-6-22710A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634636 | |||||||
| chr7:129634683 | T | C | 1 | a0001c0002t0001g0331 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-6-22663T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634683 | |||||||
| chr7:129634937 | C | T | 1 | a0001c0003t0001g0017 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-6-22409C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634937 | |||||||
| chr7:129634987 | C | T | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-22359C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129634987 | |||||||
| chr7:129635158 | T | G | 2 | a0001c0001t0002g0079 a0001c0001t0002g0103 |
2 | HG00408.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.-6-22188T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129635158 | |||||||
| chr7:129635187 | A | G | 1 | a0001c0002t0001g0349 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-6-22159A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129635187 | |||||||
| chr7:129635439 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-6-21907G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129635439 | |||||||
| chr7:129635503 | C | A | 5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-21843C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129635503 | |||||||
| chr7:129635520 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-6-21826A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129635520 | |||||||
| chr7:129635731 | C | T | 1 | a0001c0002t0002g0265 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-6-21615C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129635731 | |||||||
| chr7:129636040 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6-21306G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129636040 | |||||||
| chr7:129636209 | C | A | 3 | a0001c0002t0001g0345 a0001c0002t0001g0363 a0001c0002t0001g0364 |
3 | NA18946.hp2 NA18957.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-6-21137C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129636209 | |||||||
| chr7:129636214 | T | TTTAA | 59 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6-21130_-6-21129i others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129636214 | ||||||
| chr7:129636523 | C | G | 2 | a0001c0001t0001g0358 a0001c0002t0001g0357 |
2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-6-20823C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129636523 | |||||||
| chr7:129636776 | G | A | 11 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6-20570G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129636776 | |||||||
| chr7:129637071 | T | C | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-20275T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637071 | |||||||
| chr7:129637100 | A | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0073 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.-6-20246A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637100 | |||||||
| chr7:129637109 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-6-20237C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637109 | |||||||
| chr7:129637252 | GA | G | 58 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(55): Show |
58 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-6-20080delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129637252 | ||||||
| chr7:129637504 | A | C | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-6-19842A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637504 | |||||||
| chr7:129637504 | A | T | 5 | a0001c0002t0001g0349 a0001c0002t0003g0352 a0001c0002t0005g0344 others(2): Show |
5 | HG01433.hp2 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-19842A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637504 | |||||||
| chr7:129637558 | A | AT | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-19787dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129637558 | ||||||
| chr7:129637583 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG01891.hp2 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-19763G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637583 | |||||||
| chr7:129637590 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-6-19756T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637590 | |||||||
| chr7:129637591 | T | A | 58 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(55): Show |
58 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-6-19755T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637591 | |||||||
| chr7:129637647 | C | T | 59 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6-19699C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637647 | |||||||
| chr7:129637736 | T | C | 1 | a0001c0002t0003g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-6-19610T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637736 | |||||||
| chr7:129637739 | C | A | 4 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0155 others(1): Show |
4 | HG01243.hp2 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-19607C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637739 | |||||||
| chr7:129637787 | G | A | 1 | a0001c0002t0003g0253 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-6-19559G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637787 | |||||||
| chr7:129637850 | A | AT | 52 | a0001c0001t0001g0196 a0001c0002t0002g0265 a0001c0002t0003g0228 others(49): Show |
52 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.-6-19489dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129637850 | ||||||
| chr7:129637869 | T | A | 1 | a0001c0001t0002g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-6-19477T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637869 | |||||||
| chr7:129637870 | T | A | 32 | a0001c0001t0001g0126 a0001c0001t0002g0026 a0001c0001t0002g0028 others(29): Show |
32 | HG00673.hp1 HG00733.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.-6-19476T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637870 | |||||||
| chr7:129637871 | T | A | 13 | a0001c0001t0002g0047 a0001c0001t0002g0062 a0001c0001t0002g0079 others(10): Show |
13 | HG00408.hp1 HG00544.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-19475T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637871 | |||||||
| chr7:129637872 | TG | T | 3 | a0001c0001t0002g0045 a0001c0001t0002g0072 a0001c0001t0002g0089 |
3 | HG00609.hp2 NA18946.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.-6-19473delG | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637872 | |||||||
| chr7:129637873 | G | T | 108 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(105): Show |
108 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-6-19473G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637873 | |||||||
| chr7:129637874 | T | A | 1 | a0001c0001t0002g0109 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-6-19472T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637874 | |||||||
| chr7:129637900 | A | G | 1 | a0001c0002t0001g0332 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-6-19446A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129637900 | |||||||
| chr7:129638112 | T | C | 3 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0067 |
3 | NA18998.hp1 NA19055.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-6-19234T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129638112 | |||||||
| chr7:129638483 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-6-18863C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129638483 | |||||||
| chr7:129638532 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-6-18814C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129638532 | |||||||
| chr7:129638640 | T | C | 12 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 others(9): Show |
12 | HG00408.hp1 HG00544.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-18706T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129638640 | |||||||
| chr7:129638646 | T | C | 3 | a0001c0002t0004g0233 a0001c0002t0004g0234 a0001c0002t0016g0232 |
3 | HG00140.hp2 HG01168.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-6-18700T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129638646 | |||||||
| chr7:129638772 | C | G | 59 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6-18574C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129638772 | |||||||
| chr7:129638870 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-6-18476C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129638870 | |||||||
| chr7:129638962 | C | T | 2 | a0001c0002t0003g0236 a0001c0002t0003g0238 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-6-18384C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129638962 | |||||||
| chr7:129638986 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-6-18360T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129638986 | |||||||
| chr7:129639313 | T | C | 1 | a0001c0002t0001g0349 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-6-18033T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129639313 | |||||||
| chr7:129639492 | G | C | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-17854G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129639492 | |||||||
| chr7:129639545 | C | CT | 6 | a0001c0002t0001g0364 a0001c0002t0001g0375 a0001c0002t0004g0298 others(3): Show |
6 | HG02027.hp2 HG02559.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-17785dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129639545 | ||||||
| chr7:129639545 | CT | C | 268 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(265): Show |
268 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-6-17785delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129639545 | ||||||
| chr7:129639545 | CTT | C | 7 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(4): Show |
7 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-17786_-6-17785d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129639545 | ||||||
| chr7:129639651 | C | T | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-17695C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129639651 | |||||||
| chr7:129639683 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-6-17663G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129639683 | |||||||
| chr7:129639695 | A | T | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-6-17651A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129639695 | |||||||
| chr7:129639780 | T | G | 106 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(103): Show |
106 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-6-17566T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129639780 | |||||||
| chr7:129640359 | A | AG | 111 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(108): Show |
111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-6-16987_-6-16986i others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129640359 | |||||||
| chr7:129640640 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-6-16706A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129640640 | |||||||
| chr7:129640667 | G | A | 55 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(52): Show |
55 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-6-16679G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129640667 | |||||||
| chr7:129640798 | CACAATTT others(11): Show |
C | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG01496.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-6-16544_-6-16527d others(20): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129640798 | ||||||
| chr7:129640859 | C | T | 2 | a0001c0003t0001g0347 a0001c0003t0001g0348 |
2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.-6-16487C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129640859 | |||||||
| chr7:129640934 | A | G | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-16412A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129640934 | |||||||
| chr7:129641344 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0059 |
2 | HG01993.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-6-16002A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641344 | |||||||
| chr7:129641348 | CCTG | C | 3 | a0001c0003t0001g0015 a0001c0003t0001g0016 a0001c0003t0001g0020 |
3 | HG01099.hp1 HG01109.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-6-15997_-6-15995d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641348 | |||||||
| chr7:129641353 | A | G | 3 | a0001c0003t0001g0015 a0001c0003t0001g0016 a0001c0003t0001g0020 |
3 | HG01099.hp1 HG01109.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-6-15993A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641353 | |||||||
| chr7:129641423 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-6-15923C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641423 | |||||||
| chr7:129641596 | T | C | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0132 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-15750T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641596 | |||||||
| chr7:129641633 | T | C | 1 | a0001c0002t0001g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-6-15713T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641633 | |||||||
| chr7:129641749 | G | A | 111 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(108): Show |
111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-6-15597G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641749 | |||||||
| chr7:129641838 | C | T | 3 | a0001c0002t0003g0352 a0001c0002t0005g0350 a0001c0002t0005g0353 |
3 | HG01433.hp2 HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-6-15508C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641838 | |||||||
| chr7:129641872 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-6-15474A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641872 | |||||||
| chr7:129641894 | T | A | 1 | a0001c0002t0001g0342 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-6-15452T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641894 | |||||||
| chr7:129641901 | G | A | 2 | a0001c0001t0002g0149 a0001c0001t0002g0150 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-6-15445G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641901 | |||||||
| chr7:129641907 | C | A | 111 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(108): Show |
111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-6-15439C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641907 | |||||||
| chr7:129641926 | G | A | 3 | a0001c0002t0001g0345 a0001c0002t0001g0363 a0001c0002t0001g0364 |
3 | NA18946.hp2 NA18957.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-6-15420G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129641926 | |||||||
| chr7:129642078 | C | A | 344 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(341): Show |
344 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.-6-15268C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642078 | |||||||
| chr7:129642235 | C | T | 5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-15111C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642235 | |||||||
| chr7:129642541 | C | T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(13): Show |
16 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-6-14805C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642541 | |||||||
| chr7:129642713 | C | G | 7 | a0001c0001t0017g0139 a0001c0002t0001g0349 a0001c0002t0003g0352 others(4): Show |
7 | HG01433.hp2 HG01943.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-14633C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642713 | |||||||
| chr7:129642751 | TA | T | 137 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(134): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-6-14589delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129642751 | ||||||
| chr7:129642751 | TAA | T | 4 | a0001c0002t0004g0234 a0001c0002t0004g0320 a0001c0002t0005g0308 others(1): Show |
4 | HG01168.hp2 NA18964.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-14590_-6-14589d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129642751 | ||||||
| chr7:129642756 | A | ACTTTTTT others(302): Show |
1 | a0001c0001t0002g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(311): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(313): Show |
2 | a0001c0001t0007g0086 a0001c0001t0007g0087 |
2 | NA18984.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(322): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(320): Show |
1 | a0001c0001t0009g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(329): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(329): Show |
1 | a0001c0001t0002g0060 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(338): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(306): Show |
1 | a0001c0001t0007g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(315): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(310): Show |
5 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0049 others(2): Show |
5 | HG01123.hp1 HG01255.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(319): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(312): Show |
3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 |
3 | HG02004.hp2 HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(321): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(315): Show |
1 | a0001c0001t0002g0103 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(324): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(317): Show |
6 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0066 others(3): Show |
6 | HG02083.hp2 NA18966.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(326): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(318): Show |
3 | a0001c0001t0002g0065 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | NA18949.hp1 NA18995.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(327): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(319): Show |
1 | a0001c0001t0002g0085 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(328): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(320): Show |
4 | a0001c0001t0002g0062 a0001c0001t0002g0080 a0001c0001t0002g0081 others(1): Show |
4 | NA18944.hp2 NA18970.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(329): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(321): Show |
2 | a0001c0001t0002g0079 a0001c0001t0002g0082 |
2 | HG00408.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(330): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(322): Show |
1 | a0001c0001t0007g0074 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(331): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(328): Show |
3 | a0001c0001t0002g0030 a0001c0001t0002g0061 a0001c0001t0007g0095 |
3 | NA18945.hp1 NA19064.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(337): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(332): Show |
1 | a0001c0001t0002g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(341): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(334): Show |
1 | a0001c0001t0007g0108 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(343): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(343): Show |
1 | a0001c0001t0002g0029 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(352): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(355): Show |
1 | a0001c0001t0002g0028 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(364): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(311): Show |
1 | a0001c0001t0002g0036 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(320): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(318): Show |
1 | a0001c0001t0002g0072 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(327): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(319): Show |
2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | NA18968.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(328): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(320): Show |
1 | a0001c0001t0002g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(329): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(322): Show |
1 | a0001c0001t0002g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(331): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(308): Show |
2 | a0001c0001t0002g0055 a0001c0001t0002g0057 |
2 | NA18980.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(317): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(309): Show |
1 | a0001c0001t0002g0056 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(318): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(339): Show |
1 | a0001c0001t0002g0075 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(348): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(346): Show |
1 | a0001c0001t0002g0026 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(355): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(309): Show |
1 | a0001c0001t0002g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(318): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(313): Show |
1 | a0001c0001t0002g0090 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(322): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(314): Show |
1 | a0001c0001t0002g0092 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(323): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(320): Show |
1 | a0001c0001t0002g0032 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(329): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(316): Show |
2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(325): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(333): Show |
2 | a0001c0001t0002g0031 a0001c0001t0002g0073 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(342): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(313): Show |
1 | a0001c0001t0002g0107 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(322): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(333): Show |
1 | a0001c0001t0002g0052 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(342): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(362): Show |
1 | a0001c0001t0002g0105 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(371): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(329): Show |
1 | a0001c0001t0002g0093 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(338): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(330): Show |
1 | a0001c0001t0002g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(339): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(333): Show |
1 | a0001c0001t0002g0097 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(342): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(334): Show |
2 | a0001c0001t0002g0021 a0001c0001t0002g0047 |
2 | NA18982.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-6-14590_-6-14589i others(343): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(345): Show |
1 | a0001c0001t0002g0100 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(354): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(335): Show |
1 | a0001c0001t0002g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(344): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(339): Show |
1 | a0001c0001t0002g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(348): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(343): Show |
1 | a0001c0001t0002g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(352): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(322): Show |
1 | a0001c0001t0002g0101 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(331): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(334): Show |
1 | a0001c0001t0002g0096 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(343): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(323): Show |
1 | a0001c0001t0002g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(332): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(329): Show |
1 | a0001c0001t0002g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(338): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(335): Show |
1 | a0001c0001t0002g0053 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(344): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(343): Show |
1 | a0001c0001t0002g0040 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(352): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(366): Show |
1 | a0001c0001t0002g0089 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(375): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(344): Show |
1 | a0001c0001t0002g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(353): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(350): Show |
1 | a0001c0001t0002g0048 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(359): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(342): Show |
1 | a0001c0001t0002g0041 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(351): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(339): Show |
1 | a0001c0001t0002g0054 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(348): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(334): Show |
1 | a0001c0001t0002g0099 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(343): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(340): Show |
1 | a0001c0001t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(349): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | A | ACTTTTTT others(363): Show |
1 | a0001c0001t0002g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-6-14590_-6-14589i others(372): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642756 | AAT | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(6): Show |
9 | HG01099.hp2 HG01943.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6-14589_-6-14588d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642756 | |||||||
| chr7:129642757 | A | C | 52 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0002g0022 others(49): Show |
52 | HG00423.hp2 HG00621.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-6-14589A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642757 | |||||||
| chr7:129642757 | A | T | 139 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-6-14589A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642757 | |||||||
| chr7:129642757 | AT | A | 10 | a0001c0002t0001g0345 a0001c0002t0001g0357 a0001c0002t0001g0363 others(7): Show |
10 | HG01069.hp1 HG01168.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-6-14570delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129642757 | ||||||
| chr7:129642758 | T | A | 1 | a0001c0002t0003g0238 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-6-14588T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642758 | |||||||
| chr7:129642758 | T | C | 82 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(79): Show |
82 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.-6-14588T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642758 | |||||||
| chr7:129642759 | T | C | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(6): Show |
9 | HG01099.hp2 HG01943.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-6-14587T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642759 | |||||||
| chr7:129642776 | T | A | 1 | a0001c0001t0002g0058 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-6-14570T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642776 | |||||||
| chr7:129642867 | C | T | 1 | a0001c0002t0005g0278 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-6-14479C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642867 | |||||||
| chr7:129642919 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-6-14427C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129642919 | |||||||
| chr7:129643074 | G | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-14272G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643074 | |||||||
| chr7:129643116 | A | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01099.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-14230A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643116 | |||||||
| chr7:129643639 | A | G | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-13707A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643639 | |||||||
| chr7:129643696 | T | C | 4 | a0001c0002t0003g0283 a0001c0002t0003g0285 a0001c0002t0003g0286 others(1): Show |
4 | HG00639.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-13650T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643696 | |||||||
| chr7:129643735 | T | C | 1 | a0001c0002t0004g0346 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-6-13611T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643735 | |||||||
| chr7:129643812 | G | A | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-13534G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643812 | |||||||
| chr7:129643858 | A | G | 72 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(69): Show |
72 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-6-13488A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643858 | |||||||
| chr7:129643935 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-6-13411C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643935 | |||||||
| chr7:129643938 | G | A | 1 | a0001c0002t0001g0384 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-6-13408G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643938 | |||||||
| chr7:129643981 | G | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-13365G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129643981 | |||||||
| chr7:129644111 | C | G | 2 | a0001c0002t0001g0359 a0001c0002t0001g0360 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-6-13235C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129644111 | |||||||
| chr7:129644327 | G | A | 1 | a0001c0002t0003g0243 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-6-13019G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129644327 | |||||||
| chr7:129644342 | A | G | 59 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-6-13004A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129644342 | |||||||
| chr7:129644349 | G | A | 1 | a0001c0002t0001g0365 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-6-12997G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129644349 | |||||||
| chr7:129644706 | A | G | 2 | a0001c0001t0002g0131 a0001c0001t0009g0135 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-6-12640A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129644706 | |||||||
| chr7:129644717 | G | A | 1 | a0001c0002t0004g0336 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-6-12629G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129644717 | |||||||
| chr7:129645046 | TA | T | 58 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(55): Show |
58 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.-6-12283delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129645046 | ||||||
| chr7:129645352 | C | T | 1 | a0001c0002t0001g0374 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-6-11994C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129645352 | |||||||
| chr7:129645533 | A | G | 16 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(13): Show |
16 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-6-11813A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129645533 | |||||||
| chr7:129645534 | C | T | 1 | a0001c0001t0002g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-6-11812C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129645534 | |||||||
| chr7:129645541 | C | T | 1 | a0001c0002t0001g0349 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-6-11805C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129645541 | |||||||
| chr7:129645555 | G | A | 338 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(335): Show |
338 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.-6-11791G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129645555 | |||||||
| chr7:129645793 | A | G | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-6-11553A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129645793 | |||||||
| chr7:129645916 | C | T | 1 | a0001c0002t0001g0382 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-6-11430C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129645916 | |||||||
| chr7:129646011 | G | A | 1 | a0001c0002t0003g0244 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-6-11335G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646011 | |||||||
| chr7:129646134 | G | A | 199 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(196): Show |
199 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.-6-11212G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646134 | |||||||
| chr7:129646529 | G | A | 1 | a0001c0002t0001g0357 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-6-10817G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646529 | |||||||
| chr7:129646565 | T | G | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-10781T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646565 | |||||||
| chr7:129646568 | T | G | 221 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(218): Show |
221 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.-6-10778T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646568 | |||||||
| chr7:129646596 | A | G | 95 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(92): Show |
95 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-6-10750A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646596 | |||||||
| chr7:129646761 | A | G | 1 | a0001c0001t0002g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-6-10585A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646761 | |||||||
| chr7:129646793 | G | A | 8 | a0001c0001t0002g0062 a0001c0001t0002g0080 a0001c0001t0002g0081 others(5): Show |
8 | HG00438.hp2 HG02027.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-10553G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646793 | |||||||
| chr7:129646828 | G | A | 1 | a0001c0002t0001g0383 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-6-10518G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646828 | |||||||
| chr7:129646854 | G | A | 2 | a0001c0002t0003g0288 a0001c0002t0003g0334 |
2 | HG01123.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-6-10492G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646854 | |||||||
| chr7:129646856 | T | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0040 |
2 | NA18957.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.-6-10490T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646856 | |||||||
| chr7:129646974 | A | T | 1 | a0001c0001t0002g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-6-10372A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129646974 | |||||||
| chr7:129647099 | G | A | 11 | a0001c0001t0001g0184 a0001c0001t0001g0198 a0001c0001t0001g0199 others(8): Show |
11 | HG00673.hp2 HG01361.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6-10247G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647099 | |||||||
| chr7:129647112 | A | C | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-10234A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647112 | |||||||
| chr7:129647225 | G | T | 105 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(102): Show |
105 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-6-10121G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647225 | |||||||
| chr7:129647295 | T | G | 1 | a0001c0001t0002g0073 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-6-10051T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647295 | |||||||
| chr7:129647299 | G | A | 4 | a0001c0002t0004g0230 a0001c0002t0004g0292 a0001c0002t0004g0295 others(1): Show |
4 | HG03831.hp1 NA18975.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-10047G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647299 | |||||||
| chr7:129647382 | A | G | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0013g0121 |
3 | HG00733.hp2 HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-6-9964A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647382 | |||||||
| chr7:129647404 | C | CT | 16 | a0001c0001t0001g0209 a0001c0001t0002g0021 a0001c0001t0002g0071 others(13): Show |
16 | HG01361.hp2 HG01943.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.-6-9926dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129647404 | ||||||
| chr7:129647674 | G | A | 1 | a0001c0003t0001g0017 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-6-9672G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647674 | |||||||
| chr7:129647713 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-6-9633G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647713 | |||||||
| chr7:129647781 | T | A | 110 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-6-9565T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647781 | |||||||
| chr7:129647839 | C | T | 1 | a0001c0002t0005g0278 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-6-9507C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647839 | |||||||
| chr7:129647979 | A | G | 1 | a0001c0002t0005g0350 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-6-9367A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129647979 | |||||||
| chr7:129648081 | G | T | 7 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(4): Show |
7 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-9265G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129648081 | |||||||
| chr7:129648270 | T | C | 105 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(102): Show |
105 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-6-9076T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129648270 | |||||||
| chr7:129648274 | C | CT | 34 | a0001c0001t0001g0024 a0001c0001t0002g0058 a0001c0001t0017g0139 others(31): Show |
34 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-6-9049dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129648274 | ||||||
| chr7:129648274 | CT | C | 111 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0126 others(108): Show |
111 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-6-9049delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129648274 | ||||||
| chr7:129648274 | CTT | C | 71 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(68): Show |
71 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.-6-9050_-6-9049del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129648274 | ||||||
| chr7:129648343 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-6-9003A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129648343 | |||||||
| chr7:129648469 | CGG | C | 15 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0039 others(12): Show |
15 | HG00438.hp1 HG01261.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6-8874_-6-8873del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129648469 | ||||||
| chr7:129648472 | G | C | 15 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0039 others(12): Show |
15 | HG00438.hp1 HG01261.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.-6-8874G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129648472 | |||||||
| chr7:129648492 | G | C | 1 | a0001c0001t0002g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-6-8854G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129648492 | |||||||
| chr7:129648653 | A | T | 5 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0005g0328 others(2): Show |
5 | HG00099.hp2 HG01256.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-6-8693A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129648653 | |||||||
| chr7:129648680 | A | C | 1 | a0001c0002t0001g0372 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-6-8666A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129648680 | |||||||
| chr7:129648917 | AT | A | 50 | a0001c0001t0002g0156 a0001c0002t0002g0265 a0001c0002t0003g0228 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-6-8415delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129648917 | ||||||
| chr7:129649297 | G | C | 1 | a0001c0001t0002g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-6-8049G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129649297 | |||||||
| chr7:129649622 | A | T | 1 | a0001c0002t0001g0384 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-6-7724A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129649622 | |||||||
| chr7:129649697 | CAG | C | 220 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(217): Show |
220 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.-6-7644_-6-7643del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129649697 | ||||||
| chr7:129649714 | C | T | 2 | a0001c0002t0001g0359 a0001c0002t0001g0360 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-6-7632C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129649714 | |||||||
| chr7:129649717 | A | G | 22 | a0001c0001t0002g0058 a0001c0003t0001g0001 a0001c0003t0001g0002 others(19): Show |
22 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-6-7629A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129649717 | |||||||
| chr7:129649816 | C | T | 117 | a0001c0002t0001g0164 a0001c0002t0001g0331 a0001c0002t0001g0332 others(114): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.-6-7530C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129649816 | |||||||
| chr7:129649872 | G | A | 1 | a0001c0002t0001g0362 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-6-7474G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129649872 | |||||||
| chr7:129649934 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-6-7412G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129649934 | |||||||
| chr7:129649992 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-6-7354A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129649992 | |||||||
| chr7:129650172 | C | CT | 8 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0151 others(5): Show |
8 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-7160dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129650172 | ||||||
| chr7:129650418 | T | C | 1 | a0001c0002t0003g0252 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-6-6928T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129650418 | |||||||
| chr7:129650481 | G | T | 1 | a0001c0001t0002g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-6-6865G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129650481 | |||||||
| chr7:129650719 | G | A | 55 | a0001c0002t0001g0164 a0001c0002t0002g0265 a0001c0002t0003g0228 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-6-6627G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129650719 | |||||||
| chr7:129651289 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-6-6057G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129651289 | |||||||
| chr7:129651419 | C | CA | 116 | a0001c0001t0001g0159 a0001c0002t0001g0331 a0001c0002t0001g0332 others(113): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-6-5911dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129651419 | ||||||
| chr7:129651419 | CA | C | 200 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(197): Show |
200 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.-6-5911delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129651419 | ||||||
| chr7:129651440 | TAGAG | T | 61 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0340 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.-6-5903_-6-5900del others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129651440 | ||||||
| chr7:129651524 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-6-5822C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129651524 | |||||||
| chr7:129651714 | G | A | 1 | a0001c0002t0001g0362 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-6-5632G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129651714 | |||||||
| chr7:129651720 | A | G | 1 | a0001c0002t0004g0318 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-6-5626A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129651720 | |||||||
| chr7:129651795 | G | C | 1 | a0001c0002t0001g0362 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-6-5551G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129651795 | |||||||
| chr7:129651891 | A | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-5455A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129651891 | |||||||
| chr7:129652107 | C | T | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-5239C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129652107 | |||||||
| chr7:129652248 | A | G | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0132 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-5098A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129652248 | |||||||
| chr7:129652311 | A | T | 1 | a0001c0002t0004g0313 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-6-5035A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129652311 | |||||||
| chr7:129652334 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-6-5012A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129652334 | |||||||
| chr7:129652368 | A | T | 2 | a0001c0002t0003g0252 a0001c0002t0003g0263 |
2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-6-4978A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129652368 | |||||||
| chr7:129652450 | A | G | 22 | a0001c0001t0002g0058 a0001c0003t0001g0001 a0001c0003t0001g0002 others(19): Show |
22 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-6-4896A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129652450 | |||||||
| chr7:129652691 | C | T | 1 | a0001c0002t0003g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-6-4655C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129652691 | |||||||
| chr7:129652776 | T | C | 1 | a0001c0002t0004g0313 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-6-4570T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129652776 | |||||||
| chr7:129652889 | G | A | 4 | a0001c0002t0001g0374 a0001c0002t0001g0375 a0001c0002t0006g0380 others(1): Show |
4 | HG00642.hp2 HG01074.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-4457G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129652889 | |||||||
| chr7:129653153 | A | C | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-6-4193A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129653153 | |||||||
| chr7:129653571 | C | A | 1 | a0001c0001t0002g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-6-3775C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129653571 | |||||||
| chr7:129653704 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-6-3642G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129653704 | |||||||
| chr7:129653705 | A | G | 1 | a0001c0001t0002g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-6-3641A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129653705 | |||||||
| chr7:129653707 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-6-3639G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129653707 | |||||||
| chr7:129653729 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-6-3617G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129653729 | |||||||
| chr7:129653839 | C | T | 7 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(4): Show |
7 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-6-3507C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129653839 | |||||||
| chr7:129653981 | C | A | 338 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(335): Show |
338 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.-6-3365C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129653981 | |||||||
| chr7:129653992 | C | T | 5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-3354C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129653992 | |||||||
| chr7:129654011 | A | T | 1 | a0001c0002t0004g0302 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-6-3335A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654011 | |||||||
| chr7:129654098 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-6-3248A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654098 | |||||||
| chr7:129654126 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-6-3220A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654126 | |||||||
| chr7:129654138 | G | A | 55 | a0001c0002t0001g0164 a0001c0002t0002g0265 a0001c0002t0003g0228 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-6-3208G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654138 | |||||||
| chr7:129654257 | T | C | 1 | a0001c0002t0005g0296 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-6-3089T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654257 | |||||||
| chr7:129654262 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-6-3084A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654262 | |||||||
| chr7:129654347 | C | G | 1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-6-2999C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654347 | |||||||
| chr7:129654411 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-6-2935G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654411 | |||||||
| chr7:129654447 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-6-2899A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654447 | |||||||
| chr7:129654459 | T | A | 3 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 |
3 | HG01261.hp2 HG01433.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.-6-2887T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654459 | |||||||
| chr7:129654703 | T | A | 1 | a0001c0001t0003g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-6-2643T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129654703 | |||||||
| chr7:129655102 | C | T | 220 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(217): Show |
220 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.-6-2244C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129655102 | |||||||
| chr7:129655104 | A | G | 1 | a0001c0002t0001g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-6-2242A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129655104 | |||||||
| chr7:129655330 | T | G | 1 | a0001c0002t0001g0349 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-6-2016T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129655330 | |||||||
| chr7:129655466 | C | G | 2 | a0001c0002t0003g0275 a0001c0002t0003g0276 |
2 | NA18941.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-6-1880C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129655466 | |||||||
| chr7:129655522 | C | CT | 247 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(244): Show |
247 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-6-1813dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129655522 | ||||||
| chr7:129655522 | CT | C | 22 | a0001c0002t0001g0367 a0001c0003t0001g0001 a0001c0003t0001g0002 others(19): Show |
22 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-6-1813delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129655522 | ||||||
| chr7:129655731 | A | G | 111 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(108): Show |
111 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-6-1615A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129655731 | |||||||
| chr7:129655774 | G | A | 1 | a0001c0002t0003g0352 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-6-1572G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129655774 | |||||||
| chr7:129655952 | A | G | 338 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(335): Show |
338 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.-6-1394A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129655952 | |||||||
| chr7:129656029 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-6-1317A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129656029 | |||||||
| chr7:129656120 | G | GTT | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-1217_-6-1216dup others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129656120 | ||||||
| chr7:129656120 | GT | G | 60 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(57): Show |
60 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.-6-1216delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 129656120 | ||||||
| chr7:129656231 | A | G | 340 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(337): Show |
340 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.-6-1115A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129656231 | |||||||
| chr7:129656279 | G | A | 119 | a0001c0002t0001g0164 a0001c0002t0001g0331 a0001c0002t0001g0332 others(116): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.-6-1067G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129656279 | |||||||
| chr7:129656732 | G | T | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-614G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129656732 | |||||||
| chr7:129656809 | T | G | 1 | a0001c0002t0004g0233 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-6-537T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129656809 | |||||||
| chr7:129656871 | C | T | 64 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0340 others(61): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.-6-475C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129656871 | |||||||
| chr7:129657055 | T | C | 2 | a0001c0002t0003g0252 a0001c0002t0003g0263 |
2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-6-291T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 1/10 | chr7 | 129657055 | |||||||
| chr7:129657607 | A | AT | 139 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(136): Show |
139 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.223+52dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129657607 | ||||||
| chr7:129657607 | A | ATT | 57 | a0001c0001t0001g0190 a0001c0002t0001g0164 a0001c0002t0001g0332 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.223+51_223+52dupTT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129657607 | ||||||
| chr7:129657607 | AT | A | 6 | a0001c0001t0002g0047 a0001c0001t0002g0059 a0001c0001t0007g0074 others(3): Show |
6 | HG01993.hp1 HG02055.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+52delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129657607 | ||||||
| chr7:129657848 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.223+274C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129657848 | |||||||
| chr7:129657862 | C | T | 1 | a0001c0003t0001g0015 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.223+288C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129657862 | |||||||
| chr7:129658005 | T | C | 1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+431T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658005 | |||||||
| chr7:129658068 | A | G | 4 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(1): Show |
4 | HG01261.hp2 HG01433.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+494A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658068 | |||||||
| chr7:129658076 | A | G | 200 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(197): Show |
200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.223+502A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658076 | |||||||
| chr7:129658153 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.223+579G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658153 | |||||||
| chr7:129658168 | T | C | 1 | a0001c0002t0004g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.223+594T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658168 | |||||||
| chr7:129658175 | G | A | 113 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(110): Show |
113 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.223+601G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658175 | |||||||
| chr7:129658240 | T | C | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.223+666T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658240 | |||||||
| chr7:129658296 | C | T | 55 | a0001c0002t0001g0164 a0001c0002t0002g0265 a0001c0002t0003g0228 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.223+722C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658296 | |||||||
| chr7:129658351 | G | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.223+777G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658351 | |||||||
| chr7:129658596 | G | GA | 6 | a0001c0001t0001g0187 a0001c0001t0001g0192 a0001c0001t0002g0036 others(3): Show |
6 | HG01928.hp2 NA18941.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+1038dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129658596 | ||||||
| chr7:129658596 | GA | G | 63 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0001g0340 others(60): Show |
63 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.223+1038delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129658596 | ||||||
| chr7:129658696 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.223+1122C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658696 | |||||||
| chr7:129658752 | T | G | 10 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(7): Show |
10 | HG01099.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.223+1178T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658752 | |||||||
| chr7:129658836 | C | G | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.223+1262C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129658836 | |||||||
| chr7:129659073 | C | CT | 11 | a0001c0002t0001g0164 a0001c0002t0003g0352 a0001c0002t0004g0323 others(8): Show |
11 | HG01981.hp2 HG02055.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.223+1522dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129659073 | ||||||
| chr7:129659073 | C | CTT | 34 | a0001c0001t0001g0136 a0001c0001t0001g0140 a0001c0001t0001g0141 others(31): Show |
34 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.223+1521_223+1522d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129659073 | ||||||
| chr7:129659073 | C | CTTT | 71 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(68): Show |
71 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.223+1520_223+1522d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129659073 | ||||||
| chr7:129659073 | C | CTTTT | 100 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(97): Show |
100 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.223+1519_223+1522d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129659073 | ||||||
| chr7:129659073 | C | CTTTTT | 14 | a0001c0001t0001g0126 a0001c0001t0002g0022 a0001c0001t0002g0023 others(11): Show |
14 | HG01106.hp2 HG02055.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.223+1518_223+1522d others(7): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129659073 | ||||||
| chr7:129659073 | CT | C | 9 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0227 others(6): Show |
9 | HG00323.hp1 HG01168.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.223+1522delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129659073 | ||||||
| chr7:129659184 | C | T | 1 | a0001c0002t0001g0379 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.223+1610C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129659184 | |||||||
| chr7:129659619 | G | T | 10 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
10 | HG02083.hp2 NA18946.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.223+2045G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129659619 | |||||||
| chr7:129659822 | A | G | 110 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.223+2248A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129659822 | |||||||
| chr7:129659838 | T | C | 1 | a0001c0002t0003g0352 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.223+2264T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129659838 | |||||||
| chr7:129660050 | G | A | 220 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(217): Show |
220 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.223+2476G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129660050 | |||||||
| chr7:129660224 | ATTATGAG others(1932): Show |
A | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+2681_223+4619d others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129660224 | ||||||
| chr7:129660302 | C | G | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.223+2728C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129660302 | |||||||
| chr7:129660343 | C | T | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+2769C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129660343 | |||||||
| chr7:129660519 | G | A | 213 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(210): Show |
213 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.223+2945G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129660519 | |||||||
| chr7:129660664 | C | T | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.223+3090C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129660664 | |||||||
| chr7:129660682 | T | C | 119 | a0001c0002t0001g0164 a0001c0002t0001g0331 a0001c0002t0001g0332 others(116): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.223+3108T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129660682 | |||||||
| chr7:129661028 | T | C | 1 | a0001c0002t0001g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.223+3454T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661028 | |||||||
| chr7:129661167 | G | A | 1 | a0001c0002t0003g0290 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.223+3593G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661167 | |||||||
| chr7:129661213 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.223+3639T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661213 | |||||||
| chr7:129661578 | C | T | 1 | a0001c0002t0001g0372 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.223+4004C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661578 | |||||||
| chr7:129661579 | G | A | 5 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0044 others(2): Show |
5 | HG00609.hp2 NA18968.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+4005G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661579 | |||||||
| chr7:129661588 | CAA | C | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.223+4015_223+4016d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661588 | |||||||
| chr7:129661592 | A | C | 17 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0192 others(14): Show |
17 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.223+4018A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661592 | |||||||
| chr7:129661740 | G | T | 3 | a0001c0002t0001g0374 a0001c0002t0006g0380 a0001c0002t0006g0381 |
3 | HG00642.hp2 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.223+4166G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661740 | |||||||
| chr7:129661829 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG01167.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+4255G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661829 | |||||||
| chr7:129661886 | G | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.223+4312G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661886 | |||||||
| chr7:129661918 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG01167.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+4344C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661918 | |||||||
| chr7:129661968 | A | T | 1 | a0001c0001t0008g0128 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.223+4394A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129661968 | |||||||
| chr7:129662101 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0171 |
3 | HG01069.hp2 HG01071.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.223+4527C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662101 | |||||||
| chr7:129662153 | A | G | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | NA18945.hp2 NA18963.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+4579A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662153 | |||||||
| chr7:129662383 | A | AGT | 8 | a0001c0002t0001g0370 a0001c0002t0001g0382 a0001c0002t0001g0383 others(5): Show |
8 | HG01257.hp1 HG01346.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.223+4848_223+4849d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662383 | A | AGTGT | 3 | a0001c0002t0001g0349 a0001c0002t0005g0350 a0001c0002t0015g0351 |
3 | HG02572.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.223+4846_223+4849d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662383 | A | AGTGTGTG others(3): Show |
1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.223+4840_223+4849d others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662383 | AGT | A | 24 | a0001c0001t0001g0165 a0001c0001t0001g0175 a0001c0001t0001g0176 others(21): Show |
24 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.223+4848_223+4849d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662383 | AGTGT | A | 14 | a0001c0001t0001g0172 a0001c0001t0001g0185 a0001c0001t0001g0186 others(11): Show |
14 | HG00323.hp2 HG01168.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.223+4846_223+4849d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662383 | AGTGTGT | A | 51 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(48): Show |
51 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.223+4844_223+4849d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662383 | AGTGTGTG others(1): Show |
A | 92 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0001g0141 others(89): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.223+4842_223+4849d others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662383 | AGTGTGTG others(3): Show |
A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(112): Show |
115 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.223+4840_223+4849d others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662383 | AGTGTGTG others(5): Show |
A | 4 | a0001c0001t0002g0033 a0001c0001t0002g0040 a0001c0001t0002g0153 others(1): Show |
4 | HG01496.hp2 HG03225.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+4838_223+4849d others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662383 | AGTGTGTG others(7): Show |
A | 1 | a0001c0002t0003g0277 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.223+4836_223+4849d others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662383 | ||||||
| chr7:129662529 | A | G | 33 | a0001c0001t0001g0165 a0001c0001t0001g0175 a0001c0001t0001g0176 others(30): Show |
33 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.223+4955A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662529 | |||||||
| chr7:129662556 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.223+4982G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662556 | |||||||
| chr7:129662579 | A | G | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+5005A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662579 | |||||||
| chr7:129662600 | G | A | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.223+5026G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662600 | |||||||
| chr7:129662643 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.223+5069T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662643 | |||||||
| chr7:129662708 | A | G | 1 | a0001c0002t0003g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.223+5134A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662708 | |||||||
| chr7:129662731 | C | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01099.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+5157C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662731 | |||||||
| chr7:129662740 | G | GTTTA | 19 | a0001c0001t0001g0136 a0001c0003t0001g0001 a0001c0003t0001g0002 others(16): Show |
19 | HG00423.hp2 HG00621.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.223+5190_223+5193d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129662740 | ||||||
| chr7:129662760 | A | T | 1 | a0001c0001t0002g0097 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.223+5186A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662760 | |||||||
| chr7:129662764 | A | T | 171 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(168): Show |
171 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.223+5190A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662764 | |||||||
| chr7:129662871 | G | A | 110 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.223+5297G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662871 | |||||||
| chr7:129662873 | C | T | 31 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(28): Show |
31 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.223+5299C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662873 | |||||||
| chr7:129662958 | C | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0163 |
2 | HG01099.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.223+5384C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662958 | |||||||
| chr7:129662963 | C | T | 11 | a0001c0001t0001g0184 a0001c0001t0001g0198 a0001c0001t0001g0199 others(8): Show |
11 | HG00673.hp2 HG01361.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.223+5389C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129662963 | |||||||
| chr7:129663080 | A | G | 8 | a0001c0002t0004g0315 a0001c0002t0004g0318 a0001c0002t0004g0320 others(5): Show |
8 | NA18943.hp2 NA18947.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+5506A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663080 | |||||||
| chr7:129663262 | G | A | 110 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.223+5688G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663262 | |||||||
| chr7:129663354 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.223+5780C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663354 | |||||||
| chr7:129663412 | C | CG | 17 | a0001c0001t0001g0161 a0001c0001t0001g0188 a0001c0001t0001g0208 others(14): Show |
17 | HG00735.hp1 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.223+5842dupG | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129663412 | ||||||
| chr7:129663413 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.223+5839G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663413 | |||||||
| chr7:129663465 | A | G | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.223+5891A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663465 | |||||||
| chr7:129663473 | T | C | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.223+5899T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663473 | |||||||
| chr7:129663479 | T | C | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.223+5905T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663479 | |||||||
| chr7:129663497 | G | A | 1 | a0001c0003t0001g0014 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.223+5923G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663497 | |||||||
| chr7:129663528 | C | T | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+5954C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663528 | |||||||
| chr7:129663533 | T | C | 346 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(343): Show |
346 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.223+5959T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663533 | |||||||
| chr7:129663534 | G | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.223+5960G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663534 | |||||||
| chr7:129663538 | G | A | 2 | a0001c0002t0005g0308 a0001c0002t0005g0338 |
2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.223+5964G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663538 | |||||||
| chr7:129663603 | C | CG | 24 | a0001c0001t0001g0024 a0001c0001t0001g0123 a0001c0001t0001g0126 others(21): Show |
24 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.223+6033dupG | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129663603 | ||||||
| chr7:129663603 | C | T | 2 | a0001c0002t0003g0248 a0001c0002t0004g0298 |
2 | HG02027.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.223+6029C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663603 | |||||||
| chr7:129663612 | G | A | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+6038G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663612 | |||||||
| chr7:129663625 | C | T | 7 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(4): Show |
7 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.223+6051C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663625 | |||||||
| chr7:129663680 | C | T | 2 | a0001c0002t0003g0275 a0001c0002t0003g0276 |
2 | NA18941.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.223+6106C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663680 | |||||||
| chr7:129663688 | G | A | 8 | a0001c0002t0004g0315 a0001c0002t0004g0318 a0001c0002t0004g0320 others(5): Show |
8 | NA18943.hp2 NA18947.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+6114G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663688 | |||||||
| chr7:129663701 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.223+6127C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663701 | |||||||
| chr7:129663776 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.223+6202A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663776 | |||||||
| chr7:129663798 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.223+6224C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663798 | |||||||
| chr7:129663799 | G | A | 10 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(7): Show |
10 | HG01361.hp2 HG01433.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.223+6225G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663799 | |||||||
| chr7:129663825 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.223+6251A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663825 | |||||||
| chr7:129663885 | G | T | 200 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(197): Show |
200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.223+6311G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663885 | |||||||
| chr7:129663926 | A | G | 1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+6352A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663926 | |||||||
| chr7:129663931 | T | C | 340 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(337): Show |
340 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.223+6357T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663931 | |||||||
| chr7:129663946 | G | A | 59 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(56): Show |
59 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.223+6372G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663946 | |||||||
| chr7:129663994 | G | A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | NA18945.hp2 NA18963.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+6420G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129663994 | |||||||
| chr7:129664093 | C | T | 4 | a0001c0002t0001g0374 a0001c0002t0001g0375 a0001c0002t0006g0380 others(1): Show |
4 | HG00642.hp2 HG01074.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+6519C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129664093 | |||||||
| chr7:129664104 | A | C | 106 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(103): Show |
106 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.223+6530A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129664104 | |||||||
| chr7:129664133 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.223+6559G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129664133 | |||||||
| chr7:129664374 | C | G | 1 | a0001c0002t0003g0253 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.223+6800C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129664374 | |||||||
| chr7:129664575 | G | A | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.224-6854G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129664575 | |||||||
| chr7:129664623 | A | G | 2 | a0001c0002t0001g0223 a0001c0002t0001g0224 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.224-6806A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129664623 | |||||||
| chr7:129664666 | C | T | 1 | a0001c0002t0003g0231 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.224-6763C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129664666 | |||||||
| chr7:129664887 | G | A | 86 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(83): Show |
86 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.224-6542G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129664887 | |||||||
| chr7:129665151 | C | T | 340 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(337): Show |
340 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.224-6278C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129665151 | |||||||
| chr7:129665269 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.224-6160G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129665269 | |||||||
| chr7:129665438 | T | C | 1 | a0001c0003t0001g0011 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.224-5991T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129665438 | |||||||
| chr7:129665451 | A | G | 61 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.224-5978A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129665451 | |||||||
| chr7:129665674 | A | G | 1 | a0001c0002t0004g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.224-5755A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129665674 | |||||||
| chr7:129665840 | C | T | 1 | a0001c0003t0001g0348 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.224-5589C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129665840 | |||||||
| chr7:129665875 | G | A | 221 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(218): Show |
221 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.224-5554G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129665875 | |||||||
| chr7:129665978 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(2): Show |
5 | HG01167.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-5451T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129665978 | |||||||
| chr7:129665984 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224-5445A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129665984 | |||||||
| chr7:129666251 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.224-5178G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666251 | |||||||
| chr7:129666327 | A | T | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.224-5102A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666327 | |||||||
| chr7:129666379 | A | T | 1 | a0001c0002t0005g0327 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.224-5050A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666379 | |||||||
| chr7:129666382 | T | C | 1 | a0001c0002t0005g0350 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.224-5047T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666382 | |||||||
| chr7:129666464 | A | T | 1 | a0001c0002t0005g0333 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.224-4965A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666464 | |||||||
| chr7:129666498 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.224-4931A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666498 | |||||||
| chr7:129666563 | A | G | 17 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(14): Show |
17 | HG00423.hp2 HG00621.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.224-4866A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666563 | |||||||
| chr7:129666618 | G | C | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.224-4811G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666618 | |||||||
| chr7:129666666 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.224-4763G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666666 | |||||||
| chr7:129666805 | A | G | 2 | a0001c0002t0003g0252 a0001c0002t0003g0263 |
2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.224-4624A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666805 | |||||||
| chr7:129666844 | T | C | 1 | a0001c0002t0001g0362 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.224-4585T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666844 | |||||||
| chr7:129666865 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224-4564T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666865 | |||||||
| chr7:129666902 | A | T | 1 | a0001c0002t0005g0333 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.224-4527A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666902 | |||||||
| chr7:129666974 | A | G | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.224-4455A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129666974 | |||||||
| chr7:129667117 | G | A | 1 | a0001c0002t0001g0361 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.224-4312G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129667117 | |||||||
| chr7:129667165 | A | C | 55 | a0001c0002t0001g0164 a0001c0002t0002g0265 a0001c0002t0003g0228 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.224-4264A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129667165 | |||||||
| chr7:129667244 | C | G | 3 | a0001c0001t0002g0069 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | NA18946.hp1 NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.224-4185C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129667244 | |||||||
| chr7:129667345 | G | A | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-4084G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129667345 | |||||||
| chr7:129667450 | T | C | 1 | a0001c0003t0001g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.224-3979T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129667450 | |||||||
| chr7:129667490 | A | G | 1 | a0001c0002t0001g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.224-3939A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129667490 | |||||||
| chr7:129667603 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.224-3826G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129667603 | |||||||
| chr7:129667741 | GTATT | G | 59 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(56): Show |
59 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.224-3647_224-3644d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129667741 | ||||||
| chr7:129667741 | GTATTTAT others(1): Show |
G | 220 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(217): Show |
220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.224-3651_224-3644d others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129667741 | ||||||
| chr7:129667741 | GTATTTAT others(5): Show |
G | 85 | a0001c0001t0001g0165 a0001c0001t0001g0172 a0001c0001t0001g0173 others(82): Show |
85 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.224-3655_224-3644d others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129667741 | ||||||
| chr7:129667741 | GTATTTAT others(9): Show |
G | 8 | a0001c0001t0001g0207 a0001c0001t0002g0149 a0001c0001t0002g0150 others(5): Show |
8 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-3659_224-3644d others(18): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129667741 | ||||||
| chr7:129667741 | GTATTTAT others(17): Show |
G | 1 | a0001c0001t0001g0167 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.224-3667_224-3644d others(26): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 129667741 | ||||||
| chr7:129667797 | C | T | 21 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(18): Show |
21 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.224-3632C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129667797 | |||||||
| chr7:129667902 | G | A | 340 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(337): Show |
340 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.224-3527G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129667902 | |||||||
| chr7:129668116 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224-3313T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129668116 | |||||||
| chr7:129668185 | A | T | 1 | a0001c0002t0005g0333 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.224-3244A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129668185 | |||||||
| chr7:129668366 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.224-3063G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129668366 | |||||||
| chr7:129668454 | A | G | 54 | a0001c0002t0002g0265 a0001c0002t0003g0228 a0001c0002t0003g0229 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.224-2975A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129668454 | |||||||
| chr7:129668714 | C | T | 41 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(38): Show |
41 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.224-2715C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129668714 | |||||||
| chr7:129668720 | G | A | 41 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(38): Show |
41 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.224-2709G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129668720 | |||||||
| chr7:129668763 | C | A | 110 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.224-2666C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129668763 | |||||||
| chr7:129668964 | T | C | 110 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.224-2465T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129668964 | |||||||
| chr7:129669004 | G | A | 61 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.224-2425G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129669004 | |||||||
| chr7:129669677 | C | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.224-1752C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129669677 | |||||||
| chr7:129669694 | G | A | 5 | a0001c0002t0003g0283 a0001c0002t0003g0284 a0001c0002t0003g0285 others(2): Show |
5 | HG00639.hp1 HG01891.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.224-1735G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129669694 | |||||||
| chr7:129669706 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.224-1723G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129669706 | |||||||
| chr7:129669858 | T | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.224-1571T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129669858 | |||||||
| chr7:129669983 | G | C | 1 | a0001c0002t0004g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.224-1446G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129669983 | |||||||
| chr7:129670002 | A | T | 4 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-1427A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129670002 | |||||||
| chr7:129670005 | C | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0059 |
2 | HG01993.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.224-1424C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129670005 | |||||||
| chr7:129670075 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.224-1354G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129670075 | |||||||
| chr7:129670144 | A | G | 1 | a0001c0002t0002g0265 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.224-1285A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129670144 | |||||||
| chr7:129670196 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.224-1233G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129670196 | |||||||
| chr7:129670252 | T | C | 110 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.224-1177T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129670252 | |||||||
| chr7:129670283 | A | G | 200 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(197): Show |
200 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.224-1146A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129670283 | |||||||
| chr7:129670698 | C | G | 4 | a0001c0002t0003g0352 a0001c0002t0005g0344 a0001c0002t0005g0350 others(1): Show |
4 | HG01433.hp2 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-731C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129670698 | |||||||
| chr7:129671011 | CAG | C | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-417_224-416del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129671011 | |||||||
| chr7:129671057 | C | A | 1 | a0001c0002t0003g0253 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.224-372C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129671057 | |||||||
| chr7:129671089 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.224-340A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 2/10 | chr7 | 129671089 | |||||||
| chr7:129671727 | A | G | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.338+184A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129671727 | |||||||
| chr7:129672097 | G | C | 7 | a0001c0002t0005g0278 a0001c0002t0005g0294 a0001c0002t0005g0296 others(4): Show |
7 | HG01346.hp2 NA18939.hp1 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.338+554G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129672097 | |||||||
| chr7:129672200 | C | CT | 141 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0118 others(138): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.338+677dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129672200 | ||||||
| chr7:129672200 | C | CTT | 101 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0127 others(98): Show |
101 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.338+676_338+677dup others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129672200 | ||||||
| chr7:129672200 | C | CTTT | 28 | a0001c0001t0001g0126 a0001c0001t0002g0062 a0001c0001t0002g0080 others(25): Show |
28 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.338+675_338+677dup others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129672200 | ||||||
| chr7:129672730 | G | A | 101 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(98): Show |
101 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.338+1187G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129672730 | |||||||
| chr7:129672797 | C | G | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.338+1254C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129672797 | |||||||
| chr7:129673073 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.338+1530G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673073 | |||||||
| chr7:129673126 | A | G | 1 | a0001c0002t0003g0231 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.338+1583A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673126 | |||||||
| chr7:129673169 | A | G | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.338+1626A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673169 | |||||||
| chr7:129673245 | GGA | G | 3 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 |
3 | NA18970.hp1 NA18971.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.338+1708_338+1709d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129673245 | ||||||
| chr7:129673280 | T | C | 2 | a0001c0002t0004g0298 a0001c0002t0004g0336 |
2 | HG02027.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.338+1737T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673280 | |||||||
| chr7:129673453 | G | A | 1 | a0001c0003t0001g0013 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.338+1910G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673453 | |||||||
| chr7:129673501 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.338+1958G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673501 | |||||||
| chr7:129673533 | T | TCCTGGCT others(5): Show |
1 | a0001c0001t0001g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.338+1990_338+1991i others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673533 | |||||||
| chr7:129673585 | C | T | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.338+2042C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673585 | |||||||
| chr7:129673646 | G | A | 1 | a0001c0004t0001g0369 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.338+2103G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673646 | |||||||
| chr7:129673665 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.338+2122G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673665 | |||||||
| chr7:129673672 | G | C | 1 | a0001c0002t0004g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.338+2129G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673672 | |||||||
| chr7:129673674 | G | A | 1 | a0001c0002t0001g0370 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.338+2131G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673674 | |||||||
| chr7:129673679 | A | T | 1 | a0001c0002t0004g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.338+2136A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673679 | |||||||
| chr7:129673687 | C | A | 1 | a0001c0002t0004g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.338+2144C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673687 | |||||||
| chr7:129673702 | G | A | 339 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(336): Show |
339 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.338+2159G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673702 | |||||||
| chr7:129673703 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.338+2160C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673703 | |||||||
| chr7:129673716 | C | CA | 271 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(268): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.338+2192dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129673716 | ||||||
| chr7:129673716 | C | CAA | 36 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0222 others(33): Show |
36 | HG00597.hp2 HG01243.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.338+2191_338+2192d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129673716 | ||||||
| chr7:129673716 | C | CAAA | 22 | a0001c0001t0001g0136 a0001c0001t0002g0145 a0001c0001t0002g0156 others(19): Show |
22 | HG00423.hp2 HG00621.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.338+2190_338+2192d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129673716 | ||||||
| chr7:129673760 | G | C | 2 | a0001c0002t0003g0228 a0001c0002t0003g0229 |
2 | HG00639.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.338+2217G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673760 | |||||||
| chr7:129673794 | A | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.338+2251A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673794 | |||||||
| chr7:129673804 | A | G | 60 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0004g0138 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.338+2261A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673804 | |||||||
| chr7:129673838 | A | T | 1 | a0001c0001t0001g0222 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.338+2295A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673838 | |||||||
| chr7:129673840 | T | A | 3 | a0001c0001t0009g0135 a0001c0003t0001g0003 a0001c0003t0001g0004 |
3 | HG02145.hp1 NA18951.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.338+2297T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673840 | |||||||
| chr7:129673855 | T | C | 107 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(104): Show |
107 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.338+2312T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673855 | |||||||
| chr7:129673866 | A | C | 1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.338+2323A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673866 | |||||||
| chr7:129673880 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.338+2337C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129673880 | |||||||
| chr7:129674139 | T | TA | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.338+2610dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129674139 | ||||||
| chr7:129674149 | A | G | 223 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(220): Show |
223 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.338+2606A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129674149 | |||||||
| chr7:129674158 | T | C | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+2615T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129674158 | |||||||
| chr7:129674313 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.338+2770A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129674313 | |||||||
| chr7:129674402 | T | TA | 195 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(192): Show |
195 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.338+2870dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129674402 | ||||||
| chr7:129674428 | G | A | 166 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(163): Show |
166 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.338+2885G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129674428 | |||||||
| chr7:129674442 | C | CT | 8 | a0001c0001t0001g0202 a0001c0001t0002g0043 a0001c0001t0008g0110 others(5): Show |
8 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.338+2908dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129674442 | ||||||
| chr7:129674555 | T | G | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.338+3012T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129674555 | |||||||
| chr7:129674597 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.339-3035C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129674597 | |||||||
| chr7:129674812 | G | A | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.339-2820G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129674812 | |||||||
| chr7:129674957 | G | A | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.339-2675G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129674957 | |||||||
| chr7:129674976 | T | C | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.339-2656T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129674976 | |||||||
| chr7:129675021 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.339-2611A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129675021 | |||||||
| chr7:129675065 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.339-2567T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129675065 | |||||||
| chr7:129675602 | C | T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(12): Show |
15 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.339-2030C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129675602 | |||||||
| chr7:129675915 | T | G | 1 | a0001c0001t0002g0080 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.339-1717T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129675915 | |||||||
| chr7:129676243 | G | C | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.339-1389G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129676243 | |||||||
| chr7:129676303 | A | G | 1 | a0001c0002t0004g0235 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.339-1329A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129676303 | |||||||
| chr7:129676389 | G | A | 58 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(55): Show |
58 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.339-1243G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129676389 | |||||||
| chr7:129676399 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.339-1233G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129676399 | |||||||
| chr7:129676449 | G | C | 1 | a0001c0002t0001g0365 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.339-1183G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129676449 | |||||||
| chr7:129676476 | G | A | 1 | a0001c0002t0001g0377 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.339-1156G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129676476 | |||||||
| chr7:129676588 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.339-1044G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129676588 | |||||||
| chr7:129676631 | CACAGATC others(6): Show |
C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG00544.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.339-994_339-982del others(13): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129676631 | ||||||
| chr7:129676974 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.339-658A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129676974 | |||||||
| chr7:129677007 | A | AT | 45 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0002g0145 others(42): Show |
45 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.339-604dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129677007 | ||||||
| chr7:129677007 | A | ATT | 51 | a0001c0001t0001g0126 a0001c0001t0001g0167 a0001c0001t0001g0168 others(48): Show |
51 | HG00673.hp2 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.339-605_339-604dup others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129677007 | ||||||
| chr7:129677007 | A | ATTT | 150 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(147): Show |
150 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.339-606_339-604dup others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129677007 | ||||||
| chr7:129677007 | A | ATTTT | 77 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0190 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.339-607_339-604dup others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129677007 | ||||||
| chr7:129677007 | A | ATTTTT | 9 | a0001c0001t0002g0102 a0001c0002t0001g0341 a0001c0002t0001g0342 others(6): Show |
9 | HG02056.hp1 HG03098.hp2 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.339-608_339-604dup others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129677007 | ||||||
| chr7:129677100 | TC | T | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-530delC | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 129677100 | ||||||
| chr7:129677120 | C | T | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.339-512C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129677120 | |||||||
| chr7:129677146 | G | A | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.339-486G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129677146 | |||||||
| chr7:129677156 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.339-476G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129677156 | |||||||
| chr7:129677162 | C | T | 1 | a0001c0001t0001g0358 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.339-470C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129677162 | |||||||
| chr7:129677380 | C | A | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.339-252C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129677380 | |||||||
| chr7:129677380 | C | G | 1 | a0001c0002t0005g0294 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.339-252C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129677380 | |||||||
| chr7:129677501 | A | G | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.339-131A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129677501 | |||||||
| chr7:129677588 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.339-44C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 3/10 | chr7 | 129677588 | |||||||
| chr7:129677956 | G | A | 3 | a0001c0002t0003g0352 a0001c0002t0005g0350 a0001c0002t0005g0353 |
3 | HG01433.hp2 HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.465+198G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129677956 | |||||||
| chr7:129677973 | A | G | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0132 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+215A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129677973 | |||||||
| chr7:129677988 | G | A | 1 | a0001c0002t0012g0311 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.465+230G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129677988 | |||||||
| chr7:129677996 | G | T | 35 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(32): Show |
35 | HG01099.hp2 HG01167.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.465+238G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129677996 | |||||||
| chr7:129678132 | G | A | 3 | a0001c0003t0001g0015 a0001c0003t0001g0016 a0001c0003t0001g0020 |
3 | HG01099.hp1 HG01109.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.465+374G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129678132 | |||||||
| chr7:129678628 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.465+870T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129678628 | |||||||
| chr7:129678709 | A | G | 2 | a0001c0002t0003g0272 a0001c0002t0003g0273 |
2 | NA18971.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.465+951A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129678709 | |||||||
| chr7:129679171 | A | G | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+1413A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129679171 | |||||||
| chr7:129679458 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.465+1700A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129679458 | |||||||
| chr7:129679517 | C | T | 1 | a0001c0002t0006g0354 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.465+1759C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129679517 | |||||||
| chr7:129679613 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0039 |
2 | NA19074.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.465+1855C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129679613 | |||||||
| chr7:129679628 | C | G | 3 | a0001c0002t0001g0374 a0001c0002t0006g0380 a0001c0002t0006g0381 |
3 | HG00642.hp2 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.465+1870C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129679628 | |||||||
| chr7:129679793 | C | A | 23 | a0001c0001t0002g0021 a0001c0001t0002g0033 a0001c0001t0002g0039 others(20): Show |
23 | HG00438.hp1 HG00609.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.465+2035C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129679793 | |||||||
| chr7:129680020 | A | G | 1 | a0001c0002t0004g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.465+2262A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129680020 | |||||||
| chr7:129680199 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.465+2441T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129680199 | |||||||
| chr7:129680216 | A | T | 1 | a0001c0002t0001g0349 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.465+2458A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129680216 | |||||||
| chr7:129680304 | A | G | 1 | a0001c0002t0004g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.465+2546A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129680304 | |||||||
| chr7:129680589 | A | G | 2 | a0001c0001t0002g0048 a0001c0001t0002g0054 |
2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.465+2831A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129680589 | |||||||
| chr7:129680762 | G | A | 54 | a0001c0002t0003g0228 a0001c0002t0003g0229 a0001c0002t0003g0231 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.465+3004G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129680762 | |||||||
| chr7:129680889 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.465+3131A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129680889 | |||||||
| chr7:129681055 | G | A | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+3297G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681055 | |||||||
| chr7:129681351 | T | C | 220 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(217): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.465+3593T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681351 | |||||||
| chr7:129681381 | G | T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(13): Show |
16 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.465+3623G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681381 | |||||||
| chr7:129681463 | A | G | 220 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(217): Show |
220 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.465+3705A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681463 | |||||||
| chr7:129681483 | G | A | 58 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(55): Show |
58 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.465+3725G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681483 | |||||||
| chr7:129681484 | G | T | 1 | a0001c0001t0002g0047 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.465+3726G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681484 | |||||||
| chr7:129681602 | C | T | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.465+3844C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681602 | |||||||
| chr7:129681726 | G | A | 1 | a0001c0002t0003g0264 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.465+3968G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681726 | |||||||
| chr7:129681807 | T | C | 341 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(338): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.465+4049T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681807 | |||||||
| chr7:129681922 | C | CA | 29 | a0001c0001t0002g0043 a0001c0001t0002g0066 a0001c0001t0002g0098 others(26): Show |
29 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.465+4177dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129681922 | ||||||
| chr7:129681967 | A | G | 3 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0067 |
3 | NA18998.hp1 NA19055.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.465+4209A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681967 | |||||||
| chr7:129681971 | A | G | 1 | a0001c0001t0010g0216 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.465+4213A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129681971 | |||||||
| chr7:129682085 | CAGT | C | 283 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(280): Show |
283 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.465+4328_465+4330d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682085 | |||||||
| chr7:129682179 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.465+4421G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682179 | |||||||
| chr7:129682321 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.465+4563T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682321 | |||||||
| chr7:129682325 | A | G | 3 | a0001c0001t0002g0069 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | NA18946.hp1 NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.465+4567A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682325 | |||||||
| chr7:129682387 | G | T | 1 | a0001c0001t0002g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.465+4629G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682387 | |||||||
| chr7:129682468 | A | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.465+4710A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682468 | |||||||
| chr7:129682473 | C | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0190 |
3 | HG02258.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.465+4715C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682473 | |||||||
| chr7:129682514 | A | C | 1 | a0001c0001t0002g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.465+4756A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682514 | |||||||
| chr7:129682516 | C | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+4758C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682516 | |||||||
| chr7:129682630 | T | TA | 15 | a0001c0001t0001g0191 a0001c0001t0002g0023 a0001c0001t0002g0041 others(12): Show |
15 | HG01981.hp2 HG02056.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.465+4894dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129682630 | ||||||
| chr7:129682630 | TA | T | 59 | a0001c0001t0001g0024 a0001c0001t0001g0123 a0001c0001t0001g0127 others(56): Show |
59 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.465+4894delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129682630 | ||||||
| chr7:129682630 | TAA | T | 9 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
9 | HG02451.hp2 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+4893_465+4894d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129682630 | ||||||
| chr7:129682630 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465+4884_465+4894d others(13): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129682630 | ||||||
| chr7:129682631 | A | T | 2 | a0001c0002t0001g0376 a0001c0002t0014g0378 |
2 | HG00408.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.465+4873A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129682631 | |||||||
| chr7:129683025 | A | G | 3 | a0001c0002t0005g0301 a0001c0002t0005g0308 a0001c0002t0005g0338 |
3 | NA18964.hp1 NA19065.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.465+5267A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683025 | |||||||
| chr7:129683159 | T | C | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+5401T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683159 | |||||||
| chr7:129683284 | GGA | G | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+5530_465+5531d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683284 | ||||||
| chr7:129683288 | A | AGT | 9 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(6): Show |
9 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.465+5562_465+5563d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683288 | ||||||
| chr7:129683288 | A | AGTGT | 48 | a0001c0001t0001g0192 a0001c0002t0003g0228 a0001c0002t0003g0231 others(45): Show |
48 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.465+5560_465+5563d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683288 | ||||||
| chr7:129683288 | A | AGTGTGT | 6 | a0001c0001t0001g0172 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG00639.hp2 HG01891.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+5558_465+5563d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683288 | ||||||
| chr7:129683288 | AGT | A | 9 | a0001c0001t0001g0136 a0001c0001t0002g0145 a0001c0001t0002g0151 others(6): Show |
9 | HG01978.hp2 HG02572.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.465+5562_465+5563d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683288 | ||||||
| chr7:129683288 | AGTGT | A | 17 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(14): Show |
17 | HG00099.hp1 HG00733.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.465+5560_465+5563d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683288 | ||||||
| chr7:129683288 | AGTGTGT | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG01099.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+5558_465+5563d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683288 | ||||||
| chr7:129683288 | AGTGTGTG others(1): Show |
A | 17 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(14): Show |
17 | HG00423.hp2 HG00621.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.465+5556_465+5563d others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683288 | ||||||
| chr7:129683288 | AGTGTGTG others(3): Show |
A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(2): Show |
5 | HG01167.hp2 HG02257.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.465+5554_465+5563d others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683288 | ||||||
| chr7:129683290 | T | A | 3 | a0001c0002t0001g0345 a0001c0002t0001g0363 a0001c0002t0001g0364 |
3 | NA18946.hp2 NA18957.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.465+5532T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683290 | |||||||
| chr7:129683306 | T | A | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 |
3 | HG02970.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.465+5548T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683306 | |||||||
| chr7:129683308 | T | A | 5 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 others(2): Show |
5 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+5550T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683308 | |||||||
| chr7:129683308 | T | TGAGAGAG others(11): Show |
1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.465+5551_465+5552i others(20): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683308 | ||||||
| chr7:129683310 | T | A | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+5552T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683310 | |||||||
| chr7:129683312 | T | A | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+5554T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683312 | |||||||
| chr7:129683314 | T | A | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+5556T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683314 | |||||||
| chr7:129683316 | T | A | 12 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(9): Show |
12 | HG01099.hp1 HG01109.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.465+5558T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683316 | |||||||
| chr7:129683316 | TGTGTGA | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(3): Show |
6 | HG02135.hp1 NA18965.hp1 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+5560_465+5565d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683316 | ||||||
| chr7:129683318 | T | A | 20 | a0001c0001t0001g0136 a0001c0001t0002g0145 a0001c0001t0002g0146 others(17): Show |
20 | HG00099.hp1 HG00733.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.465+5560T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683318 | |||||||
| chr7:129683318 | T | TGA | 3 | a0001c0002t0004g0324 a0001c0002t0004g0325 a0001c0002t0004g0326 |
3 | NA18943.hp2 NA18947.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.465+5561_465+5562i others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683318 | ||||||
| chr7:129683318 | TGTGA | T | 33 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(30): Show |
33 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.465+5562_465+5565d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683318 | ||||||
| chr7:129683320 | T | A | 55 | a0001c0001t0001g0136 a0001c0001t0001g0185 a0001c0001t0001g0186 others(52): Show |
55 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.465+5562T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683320 | |||||||
| chr7:129683320 | T | TGA | 12 | a0001c0002t0001g0340 a0001c0002t0001g0362 a0001c0002t0001g0366 others(9): Show |
12 | HG00408.hp2 HG01975.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.465+5587_465+5588d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683320 | ||||||
| chr7:129683320 | TGA | T | 16 | a0001c0001t0001g0126 a0001c0001t0002g0023 a0001c0001t0002g0026 others(13): Show |
16 | HG01106.hp2 HG02055.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.465+5587_465+5588d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683320 | ||||||
| chr7:129683320 | TGAGA | T | 55 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0031 others(52): Show |
55 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.465+5585_465+5588d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683320 | ||||||
| chr7:129683322 | A | T | 11 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(8): Show |
11 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.465+5564A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683322 | |||||||
| chr7:129683324 | A | T | 6 | a0001c0001t0001g0126 a0001c0001t0002g0023 a0001c0001t0002g0041 others(3): Show |
6 | HG01106.hp2 HG02080.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.465+5566A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683324 | |||||||
| chr7:129683326 | A | T | 1 | a0001c0002t0003g0287 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.465+5568A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683326 | |||||||
| chr7:129683328 | A | T | 1 | a0001c0002t0003g0287 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.465+5570A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683328 | |||||||
| chr7:129683353 | G | T | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+5595G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683353 | |||||||
| chr7:129683365 | A | G | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.465+5607A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683365 | |||||||
| chr7:129683512 | T | C | 1 | a0001c0001t0007g0087 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.465+5754T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683512 | |||||||
| chr7:129683580 | T | G | 7 | a0001c0001t0001g0136 a0001c0001t0002g0149 a0001c0001t0002g0150 others(4): Show |
7 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.465+5822T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683580 | |||||||
| chr7:129683618 | C | G | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG01496.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.465+5860C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683618 | |||||||
| chr7:129683633 | A | AT | 205 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(202): Show |
205 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.465+5894dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683633 | ||||||
| chr7:129683633 | A | ATT | 15 | a0001c0001t0001g0142 a0001c0001t0002g0021 a0001c0001t0002g0023 others(12): Show |
15 | HG00423.hp2 HG01255.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.465+5893_465+5894d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129683633 | ||||||
| chr7:129683739 | A | G | 1 | a0001c0002t0003g0352 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.465+5981A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683739 | |||||||
| chr7:129683849 | T | G | 2 | a0001c0002t0003g0275 a0001c0002t0003g0276 |
2 | NA18941.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.465+6091T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129683849 | |||||||
| chr7:129684012 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0002g0147 |
2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.465+6254A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129684012 | |||||||
| chr7:129684038 | T | C | 1 | a0001c0002t0001g0379 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.465+6280T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129684038 | |||||||
| chr7:129684246 | CAG | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(12): Show |
15 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.466-6158_466-6157d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129684246 | ||||||
| chr7:129684413 | TAGTA | T | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-5990_466-5987d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129684413 | ||||||
| chr7:129684499 | A | G | 1 | a0001c0002t0004g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.466-5907A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129684499 | |||||||
| chr7:129684797 | A | G | 3 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 |
3 | HG02970.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.466-5609A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129684797 | |||||||
| chr7:129684883 | C | A | 1 | a0001c0002t0003g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.466-5523C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129684883 | |||||||
| chr7:129684951 | C | G | 1 | a0001c0002t0004g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.466-5455C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129684951 | |||||||
| chr7:129684952 | T | C | 1 | a0001c0002t0004g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.466-5454T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129684952 | |||||||
| chr7:129684953 | G | T | 1 | a0001c0002t0004g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.466-5453G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129684953 | |||||||
| chr7:129684976 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.466-5430A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129684976 | |||||||
| chr7:129685091 | G | A | 1 | a0001c0002t0004g0320 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.466-5315G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685091 | |||||||
| chr7:129685115 | T | A | 15 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(12): Show |
15 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.466-5291T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685115 | |||||||
| chr7:129685117 | A | T | 1 | a0001c0003t0001g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.466-5289A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685117 | |||||||
| chr7:129685126 | T | A | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-5280T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685126 | |||||||
| chr7:129685148 | A | G | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-5258A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685148 | |||||||
| chr7:129685405 | A | C | 1 | a0001c0002t0004g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.466-5001A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685405 | |||||||
| chr7:129685406 | C | A | 1 | a0001c0002t0004g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.466-5000C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685406 | |||||||
| chr7:129685407 | A | C | 1 | a0001c0002t0004g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.466-4999A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685407 | |||||||
| chr7:129685556 | A | AGT | 34 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0170 others(31): Show |
34 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.466-4803_466-4802d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | A | AGTGT | 20 | a0001c0001t0001g0197 a0001c0001t0001g0220 a0001c0001t0002g0041 others(17): Show |
20 | HG00438.hp2 HG00544.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.466-4805_466-4802d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | A | AGTGTGT | 7 | a0001c0001t0001g0207 a0001c0001t0002g0045 a0001c0001t0002g0056 others(4): Show |
7 | HG00609.hp2 HG01975.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-4807_466-4802d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0002g0114 a0001c0001t0002g0131 |
2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.466-4811_466-4802d others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGT | A | 69 | a0001c0001t0001g0024 a0001c0001t0001g0123 a0001c0001t0001g0143 others(66): Show |
69 | HG00673.hp2 HG00733.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.466-4803_466-4802d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGT | A | 63 | a0001c0001t0001g0126 a0001c0001t0001g0140 a0001c0001t0001g0141 others(60): Show |
63 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.466-4805_466-4802d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGT | A | 10 | a0001c0001t0002g0090 a0001c0001t0002g0151 a0001c0001t0002g0152 others(7): Show |
10 | HG00733.hp1 HG01168.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-4807_466-4802d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGTG others(1): Show |
A | 24 | a0001c0001t0017g0139 a0001c0002t0004g0138 a0001c0002t0004g0292 others(21): Show |
24 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.466-4809_466-4802d others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGTG others(3): Show |
A | 3 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0002t0003g0282 |
3 | HG01496.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.466-4811_466-4802d others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGTG others(5): Show |
A | 6 | a0001c0001t0001g0159 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-4813_466-4802d others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGTG others(9): Show |
A | 5 | a0001c0002t0001g0349 a0001c0002t0001g0370 a0001c0002t0011g0371 others(2): Show |
5 | HG00140.hp1 HG01346.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-4817_466-4802d others(18): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGTG others(11): Show |
A | 1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.466-4819_466-4802d others(20): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGTG others(13): Show |
A | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.466-4821_466-4802d others(22): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGTG others(15): Show |
A | 1 | a0001c0002t0003g0290 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.466-4823_466-4802d others(24): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGTG others(17): Show |
A | 47 | a0001c0002t0003g0228 a0001c0002t0003g0229 a0001c0002t0003g0231 others(44): Show |
47 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.466-4825_466-4802d others(26): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685556 | AGTGTGTG others(21): Show |
A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.466-4829_466-4802d others(30): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129685556 | ||||||
| chr7:129685582 | T | C | 2 | a0001c0002t0001g0340 a0001c0002t0001g0341 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.466-4824T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685582 | |||||||
| chr7:129685669 | G | A | 22 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(19): Show |
22 | HG01099.hp2 HG01167.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.466-4737G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685669 | |||||||
| chr7:129685826 | C | T | 1 | a0001c0002t0005g0353 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.466-4580C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685826 | |||||||
| chr7:129685956 | G | T | 1 | a0001c0002t0001g0361 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.466-4450G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129685956 | |||||||
| chr7:129686101 | C | CA | 33 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(30): Show |
33 | HG00099.hp1 HG00733.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.466-4285dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129686101 | ||||||
| chr7:129686101 | CA | C | 14 | a0001c0001t0001g0192 a0001c0001t0002g0047 a0001c0001t0002g0145 others(11): Show |
14 | HG00323.hp1 HG01361.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.466-4285delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129686101 | ||||||
| chr7:129686180 | G | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0004g0177 |
3 | HG01256.hp2 HG01258.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.466-4226G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686180 | |||||||
| chr7:129686191 | G | A | 1 | a0001c0002t0004g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.466-4215G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686191 | |||||||
| chr7:129686192 | A | G | 1 | a0001c0002t0004g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.466-4214A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686192 | |||||||
| chr7:129686217 | C | A | 62 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(59): Show |
62 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.466-4189C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686217 | |||||||
| chr7:129686292 | G | C | 31 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(28): Show |
31 | HG01099.hp2 HG01167.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.466-4114G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686292 | |||||||
| chr7:129686320 | A | G | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.466-4086A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686320 | |||||||
| chr7:129686359 | G | C | 1 | a0001c0002t0001g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.466-4047G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686359 | |||||||
| chr7:129686533 | T | G | 1 | a0001c0002t0005g0289 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.466-3873T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686533 | |||||||
| chr7:129686578 | A | G | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | NA18945.hp2 NA18963.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-3828A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686578 | |||||||
| chr7:129686704 | G | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-3702G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686704 | |||||||
| chr7:129686837 | G | A | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.466-3569G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686837 | |||||||
| chr7:129686904 | T | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0040 |
2 | NA18957.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.466-3502T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129686904 | |||||||
| chr7:129687276 | C | CT | 72 | a0001c0001t0002g0021 a0001c0001t0002g0052 a0001c0001t0002g0124 others(69): Show |
72 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.466-3114dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129687276 | ||||||
| chr7:129687276 | C | CTT | 10 | a0001c0002t0004g0138 a0001c0002t0004g0233 a0001c0002t0004g0234 others(7): Show |
10 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.466-3115_466-3114d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129687276 | ||||||
| chr7:129687523 | G | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-2883G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129687523 | |||||||
| chr7:129687556 | G | A | 47 | a0001c0002t0003g0228 a0001c0002t0003g0229 a0001c0002t0003g0231 others(44): Show |
47 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.466-2850G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129687556 | |||||||
| chr7:129687865 | G | T | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-2541G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129687865 | |||||||
| chr7:129688530 | C | T | 1 | a0001c0002t0003g0249 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.466-1876C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129688530 | |||||||
| chr7:129688550 | G | T | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.466-1856G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129688550 | |||||||
| chr7:129688626 | C | T | 2 | a0001c0002t0003g0240 a0001c0002t0003g0241 |
2 | HG01069.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.466-1780C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129688626 | |||||||
| chr7:129688688 | GAGAC | G | 6 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(3): Show |
6 | HG02818.hp1 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-1714_466-1711d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129688688 | ||||||
| chr7:129688690 | GAC | G | 27 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(24): Show |
27 | HG00408.hp2 HG01099.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.466-1714_466-1713d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129688690 | ||||||
| chr7:129688692 | C | G | 319 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(316): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.466-1714C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129688692 | |||||||
| chr7:129688720 | C | T | 2 | a0001c0003t0001g0018 a0001c0003t0001g0019 |
2 | NA18940.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.466-1686C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129688720 | |||||||
| chr7:129688723 | A | G | 309 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(306): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.466-1683A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129688723 | |||||||
| chr7:129688734 | C | T | 1 | a0001c0002t0005g0305 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.466-1672C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129688734 | |||||||
| chr7:129688898 | G | A | 120 | a0001c0001t0001g0136 a0001c0001t0002g0105 a0001c0001t0002g0106 others(117): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.466-1508G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129688898 | |||||||
| chr7:129688931 | TTG | T | 350 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(347): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.466-1458_466-1457d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 129688931 | ||||||
| chr7:129688947 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.466-1459G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129688947 | |||||||
| chr7:129689173 | A | G | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | NA18945.hp2 NA18963.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-1233A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129689173 | |||||||
| chr7:129689304 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-1102G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129689304 | |||||||
| chr7:129689421 | G | A | 61 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.466-985G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129689421 | |||||||
| chr7:129689568 | C | T | 54 | a0001c0001t0001g0136 a0001c0002t0003g0228 a0001c0002t0003g0229 others(51): Show |
54 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.466-838C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129689568 | |||||||
| chr7:129689598 | G | A | 21 | a0001c0002t0003g0231 a0001c0002t0003g0242 a0001c0002t0003g0243 others(18): Show |
21 | HG00558.hp1 HG01928.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.466-808G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129689598 | |||||||
| chr7:129689778 | C | T | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-628C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129689778 | |||||||
| chr7:129689833 | A | G | 61 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0002t0003g0290 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.466-573A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129689833 | |||||||
| chr7:129689893 | G | A | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.466-513G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129689893 | |||||||
| chr7:129690176 | C | G | 47 | a0001c0002t0003g0228 a0001c0002t0003g0229 a0001c0002t0003g0231 others(44): Show |
47 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.466-230C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 4/10 | chr7 | 129690176 | |||||||
| chr7:129690731 | C | G | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.606+185C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129690731 | |||||||
| chr7:129690982 | C | T | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.606+436C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129690982 | |||||||
| chr7:129691021 | G | A | 1 | a0001c0002t0004g0298 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.606+475G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691021 | |||||||
| chr7:129691063 | C | T | 111 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(108): Show |
111 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.606+517C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691063 | |||||||
| chr7:129691094 | G | A | 3 | a0001c0001t0002g0031 a0001c0001t0002g0073 a0001c0001t0002g0092 |
3 | HG00673.hp1 HG02074.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.606+548G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691094 | |||||||
| chr7:129691128 | A | T | 5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(2): Show |
5 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.606+582A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691128 | |||||||
| chr7:129691349 | T | TTTA | 7 | a0001c0001t0002g0145 a0001c0001t0002g0148 a0001c0001t0002g0151 others(4): Show |
7 | HG01361.hp2 HG01943.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.606+818_606+820dup others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129691349 | ||||||
| chr7:129691361 | A | AT | 51 | a0001c0001t0001g0126 a0001c0001t0001g0172 a0001c0001t0001g0180 others(48): Show |
51 | HG00639.hp1 HG00673.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.606+817dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129691361 | ||||||
| chr7:129691364 | A | AT | 218 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(215): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.606+833dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129691364 | ||||||
| chr7:129691364 | A | T | 55 | a0001c0001t0001g0126 a0001c0001t0001g0172 a0001c0001t0001g0180 others(52): Show |
55 | HG00408.hp1 HG00639.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.606+818A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691364 | |||||||
| chr7:129691366 | T | TA | 34 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(31): Show |
34 | HG00140.hp2 HG00597.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.606+820_606+821ins others(1): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691366 | |||||||
| chr7:129691367 | T | A | 27 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(24): Show |
27 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.606+821T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691367 | |||||||
| chr7:129691471 | C | T | 1 | a0001c0001t0002g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.606+925C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691471 | |||||||
| chr7:129691479 | C | T | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+933C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691479 | |||||||
| chr7:129691909 | G | A | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+1363G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691909 | |||||||
| chr7:129691972 | C | T | 1 | a0001c0002t0003g0247 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.606+1426C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129691972 | |||||||
| chr7:129692130 | C | T | 4 | a0001c0002t0003g0352 a0001c0002t0005g0344 a0001c0002t0005g0350 others(1): Show |
4 | HG01433.hp2 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+1584C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129692130 | |||||||
| chr7:129692257 | A | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.606+1711A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129692257 | |||||||
| chr7:129692293 | G | A | 3 | a0001c0002t0004g0233 a0001c0002t0004g0234 a0001c0002t0016g0232 |
3 | HG00140.hp2 HG01168.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.606+1747G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129692293 | |||||||
| chr7:129692345 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.606+1799G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129692345 | |||||||
| chr7:129692588 | A | G | 1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.606+2042A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129692588 | |||||||
| chr7:129692793 | G | A | 2 | a0001c0002t0003g0288 a0001c0002t0003g0334 |
2 | HG01123.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.606+2247G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129692793 | |||||||
| chr7:129692848 | A | G | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.606+2302A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129692848 | |||||||
| chr7:129693043 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.606+2497C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693043 | |||||||
| chr7:129693106 | T | C | 96 | a0001c0001t0001g0136 a0001c0001t0002g0145 a0001c0001t0002g0146 others(93): Show |
96 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.606+2560T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693106 | |||||||
| chr7:129693193 | G | C | 3 | a0001c0001t0007g0086 a0001c0001t0007g0087 a0001c0001t0007g0088 |
3 | NA18947.hp2 NA18984.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.606+2647G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693193 | |||||||
| chr7:129693347 | T | A | 9 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
9 | HG01361.hp2 HG01943.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+2801T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693347 | |||||||
| chr7:129693450 | C | T | 1 | a0001c0002t0003g0247 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.606+2904C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693450 | |||||||
| chr7:129693451 | G | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.606+2905G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693451 | |||||||
| chr7:129693497 | A | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.606+2951A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693497 | |||||||
| chr7:129693692 | A | G | 1 | a0001c0002t0003g0290 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.606+3146A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693692 | |||||||
| chr7:129693700 | G | A | 67 | a0001c0001t0001g0136 a0001c0001t0002g0145 a0001c0001t0002g0146 others(64): Show |
67 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.606+3154G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693700 | |||||||
| chr7:129693738 | CAT | C | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+3194_606+3195d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129693738 | ||||||
| chr7:129693913 | G | A | 1 | a0001c0002t0001g0379 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.606+3367G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129693913 | |||||||
| chr7:129694007 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0215 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.606+3461G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694007 | |||||||
| chr7:129694065 | G | A | 166 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(163): Show |
166 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.606+3519G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694065 | |||||||
| chr7:129694141 | C | T | 1 | a0001c0002t0005g0300 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.606+3595C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694141 | |||||||
| chr7:129694161 | A | T | 1 | a0001c0001t0001g0192 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.606+3615A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694161 | |||||||
| chr7:129694229 | A | G | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.606+3683A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694229 | |||||||
| chr7:129694295 | C | T | 1 | a0001c0001t0002g0035 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.606+3749C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694295 | |||||||
| chr7:129694381 | T | G | 1 | a0001c0001t0002g0058 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.606+3835T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694381 | |||||||
| chr7:129694450 | C | T | 1 | a0001c0002t0005g0333 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.606+3904C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694450 | |||||||
| chr7:129694570 | G | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+4024G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694570 | |||||||
| chr7:129694593 | C | G | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(9): Show |
12 | HG00544.hp2 HG00609.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.606+4047C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694593 | |||||||
| chr7:129694672 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.606+4126G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694672 | |||||||
| chr7:129694706 | T | C | 55 | a0001c0001t0001g0136 a0001c0002t0003g0228 a0001c0002t0003g0229 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.606+4160T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129694706 | |||||||
| chr7:129695047 | C | T | 1 | a0001c0002t0003g0286 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.606+4501C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129695047 | |||||||
| chr7:129695074 | G | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.606+4528G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129695074 | |||||||
| chr7:129695309 | G | T | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.606+4763G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129695309 | |||||||
| chr7:129695396 | G | C | 2 | a0001c0001t0008g0110 a0001c0001t0008g0111 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.606+4850G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129695396 | |||||||
| chr7:129695470 | G | A | 1 | a0001c0003t0001g0017 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.606+4924G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129695470 | |||||||
| chr7:129695575 | C | CA | 71 | a0001c0001t0001g0136 a0001c0001t0001g0190 a0001c0001t0002g0043 others(68): Show |
71 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.606+5042dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129695575 | ||||||
| chr7:129695687 | T | A | 15 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(12): Show |
15 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.606+5141T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129695687 | |||||||
| chr7:129695709 | T | C | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+5163T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129695709 | |||||||
| chr7:129696021 | G | A | 2 | a0001c0001t0002g0101 a0001c0001t0002g0102 |
2 | HG02056.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.606+5475G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129696021 | |||||||
| chr7:129696032 | G | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.606+5486G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129696032 | |||||||
| chr7:129696055 | T | C | 48 | a0001c0002t0003g0228 a0001c0002t0003g0229 a0001c0002t0003g0231 others(45): Show |
48 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.606+5509T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129696055 | |||||||
| chr7:129696060 | T | TA | 85 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0140 others(82): Show |
85 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.606+5540dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129696060 | ||||||
| chr7:129696060 | T | TAA | 74 | a0001c0001t0001g0024 a0001c0001t0001g0136 a0001c0001t0001g0142 others(71): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.606+5539_606+5540d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129696060 | ||||||
| chr7:129696060 | T | TAAA | 10 | a0001c0001t0001g0118 a0001c0002t0003g0282 a0001c0002t0004g0299 others(7): Show |
10 | HG01978.hp2 HG02717.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+5538_606+5540d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129696060 | ||||||
| chr7:129696084 | A | AAAAC | 25 | a0001c0001t0001g0077 a0001c0001t0001g0174 a0001c0001t0001g0178 others(22): Show |
25 | HG00621.hp2 HG00735.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.606+5540_606+5541i others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129696084 | ||||||
| chr7:129696084 | A | AAAC | 127 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0126 others(124): Show |
127 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.606+5542_606+5544d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129696084 | ||||||
| chr7:129696084 | A | AAC | 11 | a0001c0001t0001g0175 a0001c0001t0001g0200 a0001c0001t0002g0054 others(8): Show |
11 | HG01256.hp2 HG02965.hp2 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.606+5539_606+5540i others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129696084 | ||||||
| chr7:129696084 | A | C | 1 | a0001c0001t0002g0109 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.606+5538A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129696084 | |||||||
| chr7:129696295 | G | A | 1 | a0001c0002t0001g0361 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.606+5749G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129696295 | |||||||
| chr7:129696372 | T | G | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.606+5826T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129696372 | |||||||
| chr7:129696397 | G | T | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0013g0121 |
3 | HG00733.hp2 HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.606+5851G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129696397 | |||||||
| chr7:129697115 | A | C | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.606+6569A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697115 | |||||||
| chr7:129697132 | G | T | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+6586G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697132 | |||||||
| chr7:129697193 | C | CT | 55 | a0001c0001t0001g0136 a0001c0002t0003g0228 a0001c0002t0003g0229 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.606+6656dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129697193 | ||||||
| chr7:129697266 | G | A | 65 | a0001c0001t0001g0136 a0001c0001t0002g0149 a0001c0001t0002g0150 others(62): Show |
65 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.606+6720G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697266 | |||||||
| chr7:129697284 | A | C | 97 | a0001c0001t0001g0136 a0001c0001t0002g0145 a0001c0001t0002g0146 others(94): Show |
97 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.606+6738A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697284 | |||||||
| chr7:129697368 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.606+6822C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697368 | |||||||
| chr7:129697387 | T | A | 4 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0113 others(1): Show |
4 | HG02056.hp1 HG02258.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+6841T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697387 | |||||||
| chr7:129697405 | C | T | 1 | a0001c0002t0004g0313 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.606+6859C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697405 | |||||||
| chr7:129697602 | G | T | 1 | a0001c0002t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.606+7056G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697602 | |||||||
| chr7:129697729 | T | TTTTTTG | 74 | a0001c0001t0001g0136 a0001c0001t0002g0145 a0001c0001t0002g0146 others(71): Show |
74 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.606+7202_606+7207d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129697729 | ||||||
| chr7:129697732 | T | G | 1 | a0001c0003t0001g0015 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.606+7186T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697732 | |||||||
| chr7:129697892 | G | A | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.606+7346G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697892 | |||||||
| chr7:129697926 | G | C | 1 | a0001c0002t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.606+7380G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697926 | |||||||
| chr7:129697955 | C | G | 62 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(59): Show |
62 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.606+7409C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697955 | |||||||
| chr7:129697978 | G | A | 1 | a0001c0001t0007g0095 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.606+7432G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129697978 | |||||||
| chr7:129698341 | G | C | 74 | a0001c0001t0001g0136 a0001c0001t0002g0145 a0001c0001t0002g0146 others(71): Show |
74 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.606+7795G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129698341 | |||||||
| chr7:129698791 | A | C | 2 | a0001c0002t0003g0244 a0001c0002t0003g0255 |
2 | NA18975.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.606+8245A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129698791 | |||||||
| chr7:129698814 | T | C | 1 | a0001c0002t0005g0291 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.606+8268T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129698814 | |||||||
| chr7:129699123 | G | A | 1 | a0001c0002t0005g0297 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.606+8577G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699123 | |||||||
| chr7:129699225 | C | T | 1 | a0001c0002t0001g0349 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.606+8679C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699225 | |||||||
| chr7:129699231 | T | G | 1 | a0001c0002t0001g0383 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.606+8685T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699231 | |||||||
| chr7:129699385 | A | C | 1 | a0001c0001t0002g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.606+8839A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699385 | |||||||
| chr7:129699718 | G | C | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.606+9172G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699718 | |||||||
| chr7:129699802 | T | C | 1 | a0001c0002t0003g0286 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.606+9256T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699802 | |||||||
| chr7:129699804 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.606+9258G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699804 | |||||||
| chr7:129699833 | T | C | 1 | a0001c0001t0013g0121 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.607-9242T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699833 | |||||||
| chr7:129699910 | C | T | 5 | a0001c0002t0003g0283 a0001c0002t0003g0284 a0001c0002t0003g0285 others(2): Show |
5 | HG00639.hp1 HG01891.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-9165C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699910 | |||||||
| chr7:129699975 | T | TA | 377 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(374): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.607-9085dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129699975 | ||||||
| chr7:129699993 | T | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-9082T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699993 | |||||||
| chr7:129699998 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.607-9077G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129699998 | |||||||
| chr7:129700140 | C | CA | 24 | a0001c0002t0004g0313 a0001c0003t0001g0001 a0001c0003t0001g0002 others(21): Show |
24 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.607-8923dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129700140 | ||||||
| chr7:129700159 | G | T | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.607-8916G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129700159 | |||||||
| chr7:129700358 | C | A | 1 | a0001c0002t0005g0281 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.607-8717C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129700358 | |||||||
| chr7:129700365 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.607-8710C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129700365 | |||||||
| chr7:129700386 | A | G | 15 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(12): Show |
15 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.607-8689A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129700386 | |||||||
| chr7:129700622 | A | G | 4 | a0001c0002t0003g0352 a0001c0002t0005g0344 a0001c0002t0005g0350 others(1): Show |
4 | HG01433.hp2 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-8453A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129700622 | |||||||
| chr7:129700893 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.607-8182G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129700893 | |||||||
| chr7:129701302 | A | G | 15 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(12): Show |
15 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.607-7773A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129701302 | |||||||
| chr7:129701456 | C | T | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.607-7619C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129701456 | |||||||
| chr7:129701476 | T | G | 1 | a0001c0001t0002g0152 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.607-7599T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129701476 | |||||||
| chr7:129701591 | CA | C | 9 | a0001c0001t0001g0184 a0001c0001t0001g0199 a0001c0001t0001g0200 others(6): Show |
9 | HG00673.hp2 HG01361.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.607-7472delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129701591 | ||||||
| chr7:129701617 | A | T | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-7458A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129701617 | |||||||
| chr7:129701722 | G | A | 2 | a0001c0002t0004g0346 a0001c0002t0004g0373 |
2 | NA18955.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.607-7353G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129701722 | |||||||
| chr7:129701902 | A | T | 29 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(26): Show |
29 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.607-7173A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129701902 | |||||||
| chr7:129702041 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.607-7034T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129702041 | |||||||
| chr7:129702085 | C | T | 381 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(378): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.607-6990C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129702085 | |||||||
| chr7:129702203 | A | G | 128 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(125): Show |
128 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.607-6872A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129702203 | |||||||
| chr7:129702518 | ATC | A | 127 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(124): Show |
127 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.607-6551_607-6550d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129702518 | ||||||
| chr7:129702564 | G | A | 121 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(118): Show |
121 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.607-6511G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129702564 | |||||||
| chr7:129702741 | A | C | 104 | a0001c0001t0001g0126 a0001c0001t0002g0021 a0001c0001t0002g0022 others(101): Show |
104 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.607-6334A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129702741 | |||||||
| chr7:129702832 | T | G | 1 | a0001c0002t0003g0242 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.607-6243T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129702832 | |||||||
| chr7:129703204 | G | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.607-5871G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129703204 | |||||||
| chr7:129703344 | T | G | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.607-5731T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129703344 | |||||||
| chr7:129703510 | CTTTATTA others(24): Show |
C | 1 | a0001c0001t0002g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.607-5558_607-5528d others(33): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129703510 | ||||||
| chr7:129703615 | A | G | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.607-5460A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129703615 | |||||||
| chr7:129703665 | A | AC | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-5409dupC | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129703665 | ||||||
| chr7:129703688 | C | G | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.607-5387C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129703688 | |||||||
| chr7:129703867 | G | C | 1 | a0001c0002t0003g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.607-5208G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129703867 | |||||||
| chr7:129704080 | A | G | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | NA18945.hp2 NA18963.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-4995A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704080 | |||||||
| chr7:129704127 | T | A | 67 | a0001c0001t0001g0136 a0001c0001t0002g0149 a0001c0001t0002g0150 others(64): Show |
67 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.607-4948T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704127 | |||||||
| chr7:129704142 | G | A | 1 | a0001c0002t0001g0365 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.607-4933G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704142 | |||||||
| chr7:129704229 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.607-4846G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704229 | |||||||
| chr7:129704314 | C | T | 11 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(8): Show |
11 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.607-4761C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704314 | |||||||
| chr7:129704559 | A | G | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.607-4516A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704559 | |||||||
| chr7:129704579 | G | A | 1 | a0001c0002t0003g0283 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.607-4496G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704579 | |||||||
| chr7:129704655 | T | C | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.607-4420T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704655 | |||||||
| chr7:129704720 | T | C | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-4355T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704720 | |||||||
| chr7:129704837 | G | A | 61 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.607-4238G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704837 | |||||||
| chr7:129704845 | C | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.607-4230C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704845 | |||||||
| chr7:129704848 | T | C | 5 | a0001c0002t0001g0366 a0001c0002t0001g0367 a0001c0002t0001g0372 others(2): Show |
5 | HG01975.hp1 HG01981.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-4227T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704848 | |||||||
| chr7:129704872 | T | C | 1 | a0001c0002t0003g0247 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.607-4203T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704872 | |||||||
| chr7:129704978 | T | A | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.607-4097T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704978 | |||||||
| chr7:129704979 | A | T | 5 | a0001c0001t0002g0058 a0001c0001t0002g0109 a0001c0001t0002g0129 others(2): Show |
5 | HG01243.hp1 HG01516.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.607-4096A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129704979 | |||||||
| chr7:129705055 | A | G | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.607-4020A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705055 | |||||||
| chr7:129705197 | T | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.607-3878T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705197 | |||||||
| chr7:129705204 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.607-3871T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705204 | |||||||
| chr7:129705276 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.607-3799T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705276 | |||||||
| chr7:129705314 | G | A | 1 | a0001c0002t0003g0352 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.607-3761G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705314 | |||||||
| chr7:129705413 | C | T | 1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.607-3662C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705413 | |||||||
| chr7:129705421 | G | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-3654G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705421 | |||||||
| chr7:129705479 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.607-3596C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705479 | |||||||
| chr7:129705599 | C | T | 2 | a0001c0002t0005g0280 a0001c0002t0005g0327 |
2 | HG01167.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.607-3476C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705599 | |||||||
| chr7:129705751 | A | G | 3 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0013g0121 |
3 | HG00733.hp2 HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.607-3324A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705751 | |||||||
| chr7:129705876 | G | A | 1 | a0001c0002t0001g0383 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.607-3199G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705876 | |||||||
| chr7:129705904 | G | A | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-3171G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129705904 | |||||||
| chr7:129705940 | T | TGA | 56 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(53): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.607-3116_607-3115d others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129705940 | ||||||
| chr7:129705940 | T | TGAGA | 6 | a0001c0002t0004g0293 a0001c0002t0004g0307 a0001c0002t0004g0337 others(3): Show |
6 | NA18955.hp1 NA18972.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-3118_607-3115d others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129705940 | ||||||
| chr7:129706091 | G | A | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.607-2984G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129706091 | |||||||
| chr7:129706269 | T | C | 1 | a0001c0002t0003g0238 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.607-2806T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129706269 | |||||||
| chr7:129706433 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.607-2642G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129706433 | |||||||
| chr7:129706450 | C | T | 66 | a0001c0001t0001g0136 a0001c0001t0002g0149 a0001c0001t0002g0150 others(63): Show |
66 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.607-2625C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129706450 | |||||||
| chr7:129706621 | G | A | 1 | a0001c0002t0003g0259 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.607-2454G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129706621 | |||||||
| chr7:129706765 | C | G | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.607-2310C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129706765 | |||||||
| chr7:129706929 | T | C | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-2146T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129706929 | |||||||
| chr7:129706982 | T | TTTTTG | 20 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(17): Show |
20 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.607-2067_607-2063d others(7): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 129706982 | ||||||
| chr7:129707078 | T | G | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-1997T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129707078 | |||||||
| chr7:129707083 | T | A | 1 | a0001c0001t0007g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.607-1992T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129707083 | |||||||
| chr7:129707184 | G | A | 19 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(16): Show |
19 | HG01167.hp2 HG01361.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.607-1891G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129707184 | |||||||
| chr7:129707627 | G | A | 1 | a0001c0003t0001g0009 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.607-1448G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129707627 | |||||||
| chr7:129707716 | A | G | 1 | a0001c0001t0010g0216 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.607-1359A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129707716 | |||||||
| chr7:129707784 | C | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-1291C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129707784 | |||||||
| chr7:129707889 | G | A | 1 | a0001c0002t0014g0378 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.607-1186G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129707889 | |||||||
| chr7:129708114 | G | T | 1 | a0001c0002t0003g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.607-961G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129708114 | |||||||
| chr7:129708147 | G | A | 3 | a0001c0002t0003g0237 a0001c0002t0003g0258 a0001c0002t0003g0264 |
3 | HG00642.hp1 HG01070.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.607-928G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129708147 | |||||||
| chr7:129708211 | A | C | 320 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(317): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.607-864A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129708211 | |||||||
| chr7:129708776 | T | C | 1 | a0001c0002t0003g0247 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.607-299T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 5/10 | chr7 | 129708776 | |||||||
| chr7:129709240 | G | A | 1 | a0001c0002t0004g0260 | 1 | HG00735.hp2 | splice_region_variant&intron_variant | LOW | c.765+7G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709240 | |||||||
| chr7:129709261 | G | A | 55 | a0001c0001t0003g0183 a0001c0002t0003g0228 a0001c0002t0003g0229 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.765+28G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709261 | |||||||
| chr7:129709446 | A | C | 1 | a0001c0002t0004g0261 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.765+213A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709446 | |||||||
| chr7:129709462 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.765+229G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709462 | |||||||
| chr7:129709547 | C | T | 231 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(228): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.765+314C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709547 | |||||||
| chr7:129709674 | C | T | 2 | a0001c0001t0002g0130 a0001c0001t0002g0134 |
2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.765+441C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709674 | |||||||
| chr7:129709729 | CT | C | 33 | a0001c0001t0001g0197 a0001c0001t0002g0149 a0001c0001t0002g0150 others(30): Show |
33 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.765+514delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 129709729 | ||||||
| chr7:129709729 | CTT | C | 58 | a0001c0001t0003g0183 a0001c0001t0008g0110 a0001c0001t0008g0111 others(55): Show |
58 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.765+513_765+514del others(2): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 129709729 | ||||||
| chr7:129709733 | T | C | 61 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.765+500T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709733 | |||||||
| chr7:129709805 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.766-569G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709805 | |||||||
| chr7:129709808 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.766-566G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709808 | |||||||
| chr7:129709973 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.766-401G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129709973 | |||||||
| chr7:129710113 | A | C | 1 | a0001c0001t0003g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.766-261A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129710113 | |||||||
| chr7:129710206 | AC | A | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.766-167delC | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129710206 | |||||||
| chr7:129710330 | A | C | 66 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(63): Show |
66 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.766-44A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 6/10 | chr7 | 129710330 | |||||||
| chr7:129710745 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.963+174T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 7/10 | chr7 | 129710745 | |||||||
| chr7:129710903 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0116 |
2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.963+332G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 7/10 | chr7 | 129710903 | |||||||
| chr7:129710997 | G | C | 1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.963+426G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 7/10 | chr7 | 129710997 | |||||||
| chr7:129711182 | C | T | 4 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0155 others(1): Show |
4 | HG01243.hp2 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-293C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 7/10 | chr7 | 129711182 | |||||||
| chr7:129711236 | A | G | 1 | a0001c0002t0001g0375 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.964-239A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 7/10 | chr7 | 129711236 | |||||||
| chr7:129711285 | A | C | 1 | a0001c0001t0002g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.964-190A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 7/10 | chr7 | 129711285 | |||||||
| chr7:129711302 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.964-173C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 7/10 | chr7 | 129711302 | |||||||
| chr7:129711422 | A | C | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.964-53A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 7/10 | chr7 | 129711422 | |||||||
| chr7:129711453 | C | T | 1 | a0001c0002t0001g0370 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.964-22C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 7/10 | chr7 | 129711453 | |||||||
| chr7:129711604 | C | G | 55 | a0001c0001t0003g0183 a0001c0002t0003g0228 a0001c0002t0003g0229 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1065+28C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129711604 | |||||||
| chr7:129711638 | A | G | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0132 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065+62A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129711638 | |||||||
| chr7:129711821 | G | T | 1 | a0001c0001t0002g0093 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1065+245G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129711821 | |||||||
| chr7:129711850 | C | T | 1 | a0001c0001t0002g0101 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1065+274C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129711850 | |||||||
| chr7:129711880 | G | A | 167 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(164): Show |
167 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.1065+304G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129711880 | |||||||
| chr7:129711914 | T | G | 380 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(377): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.1065+338T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129711914 | |||||||
| chr7:129712144 | T | TATC | 347 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(344): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.1065+569_1065+571d others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 129712144 | ||||||
| chr7:129712497 | G | A | 265 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(262): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1065+921G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129712497 | |||||||
| chr7:129712728 | G | A | 4 | a0001c0002t0004g0230 a0001c0002t0004g0292 a0001c0002t0004g0298 others(1): Show |
4 | HG02027.hp2 NA18975.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065+1152G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129712728 | |||||||
| chr7:129712807 | T | C | 1 | a0001c0002t0003g0245 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1065+1231T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129712807 | |||||||
| chr7:129713025 | G | A | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1065+1449G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129713025 | |||||||
| chr7:129713093 | C | CT | 116 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0201 others(113): Show |
116 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1065+1535dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 129713093 | ||||||
| chr7:129713172 | C | T | 66 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(63): Show |
66 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1065+1596C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129713172 | |||||||
| chr7:129713176 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1065+1600A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129713176 | |||||||
| chr7:129713446 | T | C | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1065+1870T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129713446 | |||||||
| chr7:129713737 | T | C | 61 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1065+2161T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129713737 | |||||||
| chr7:129713754 | G | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065+2178G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129713754 | |||||||
| chr7:129714305 | A | T | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1065+2729A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129714305 | |||||||
| chr7:129714381 | G | A | 12 | a0001c0001t0002g0044 a0001c0001t0002g0063 a0001c0001t0002g0065 others(9): Show |
12 | HG00408.hp1 HG00544.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1065+2805G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129714381 | |||||||
| chr7:129714601 | C | T | 1 | a0001c0002t0001g0349 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1066-2618C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129714601 | |||||||
| chr7:129714813 | A | C | 56 | a0001c0001t0003g0183 a0001c0001t0013g0121 a0001c0002t0003g0228 others(53): Show |
56 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1066-2406A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129714813 | |||||||
| chr7:129715071 | G | A | 90 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(87): Show |
90 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1066-2148G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715071 | |||||||
| chr7:129715118 | T | C | 1 | a0001c0001t0003g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1066-2101T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715118 | |||||||
| chr7:129715230 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1066-1989C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715230 | |||||||
| chr7:129715635 | A | G | 1 | a0001c0002t0003g0237 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1066-1584A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715635 | |||||||
| chr7:129715713 | G | A | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1066-1506G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715713 | |||||||
| chr7:129715755 | A | C | 1 | a0001c0001t0002g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1066-1464A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715755 | |||||||
| chr7:129715769 | C | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0064 |
2 | NA19066.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1066-1450C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715769 | |||||||
| chr7:129715831 | C | T | 5 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
5 | HG02818.hp1 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1066-1388C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715831 | |||||||
| chr7:129715862 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1066-1357G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715862 | |||||||
| chr7:129715920 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1066-1299G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129715920 | |||||||
| chr7:129716009 | C | CA | 11 | a0001c0001t0001g0078 a0001c0001t0001g0194 a0001c0001t0001g0210 others(8): Show |
11 | HG00423.hp1 HG02145.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.1066-1208dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 129716009 | ||||||
| chr7:129716012 | C | A | 229 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(226): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1066-1207C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716012 | |||||||
| chr7:129716014 | A | AC | 26 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 others(23): Show |
26 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1066-1205_1066-120 others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716014 | |||||||
| chr7:129716015 | A | C | 50 | a0001c0001t0003g0183 a0001c0001t0013g0121 a0001c0002t0003g0228 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1066-1204A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716015 | |||||||
| chr7:129716017 | A | C | 3 | a0001c0003t0001g0008 a0001c0003t0001g0347 a0001c0003t0001g0348 |
3 | HG00099.hp1 HG00733.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1066-1202A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716017 | |||||||
| chr7:129716239 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1066-980A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716239 | |||||||
| chr7:129716282 | A | T | 166 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(163): Show |
166 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.1066-937A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716282 | |||||||
| chr7:129716357 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1066-862A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716357 | |||||||
| chr7:129716366 | G | A | 230 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(227): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1066-853G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716366 | |||||||
| chr7:129716549 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1066-670C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716549 | |||||||
| chr7:129716592 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1066-627C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716592 | |||||||
| chr7:129716627 | T | A | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-592T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716627 | |||||||
| chr7:129716750 | A | G | 2 | a0001c0002t0001g0370 a0001c0004t0001g0369 |
2 | HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1066-469A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129716750 | |||||||
| chr7:129716869 | C | CA | 226 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(223): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1066-336dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 129716869 | ||||||
| chr7:129716869 | CA | C | 49 | a0001c0001t0003g0183 a0001c0002t0003g0228 a0001c0002t0003g0229 others(46): Show |
49 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1066-336delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr7 | 129716869 | ||||||
| chr7:129717096 | A | G | 34 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(31): Show |
34 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1066-123A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129717096 | |||||||
| chr7:129717099 | T | G | 56 | a0001c0001t0003g0183 a0001c0001t0013g0121 a0001c0002t0003g0228 others(53): Show |
56 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1066-120T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 8/10 | chr7 | 129717099 | |||||||
| chr7:129717458 | T | C | 56 | a0001c0001t0003g0183 a0001c0001t0013g0121 a0001c0002t0003g0228 others(53): Show |
56 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1223+82T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129717458 | |||||||
| chr7:129717548 | A | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | NA18998.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1223+172A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129717548 | |||||||
| chr7:129717637 | A | G | 4 | a0001c0001t0007g0086 a0001c0001t0007g0087 a0001c0001t0007g0088 others(1): Show |
4 | NA18947.hp2 NA18965.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223+261A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129717637 | |||||||
| chr7:129717738 | T | C | 320 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(317): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1223+362T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129717738 | |||||||
| chr7:129717806 | A | G | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1223+430A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129717806 | |||||||
| chr7:129717990 | G | T | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1223+614G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129717990 | |||||||
| chr7:129718005 | A | G | 1 | a0001c0002t0001g0357 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1223+629A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129718005 | |||||||
| chr7:129718109 | T | C | 1 | a0001c0002t0004g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1223+733T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129718109 | |||||||
| chr7:129718183 | C | T | 1 | a0001c0001t0001g0358 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1223+807C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129718183 | |||||||
| chr7:129718245 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1223+869G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129718245 | |||||||
| chr7:129718636 | G | A | 320 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(317): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1223+1260G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129718636 | |||||||
| chr7:129718641 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1223+1265C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129718641 | |||||||
| chr7:129718822 | C | T | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1223+1446C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129718822 | |||||||
| chr7:129718898 | C | T | 1 | a0001c0003t0001g0013 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1223+1522C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129718898 | |||||||
| chr7:129718952 | T | C | 2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | NA18999.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1223+1576T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129718952 | |||||||
| chr7:129719082 | C | T | 1 | a0001c0002t0003g0287 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1223+1706C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719082 | |||||||
| chr7:129719145 | TA | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0207 a0001c0002t0001g0331 |
3 | HG01256.hp1 HG02273.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1223+1770delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719145 | |||||||
| chr7:129719146 | A | T | 344 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(341): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.1223+1770A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719146 | |||||||
| chr7:129719226 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1223+1850G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719226 | |||||||
| chr7:129719283 | C | T | 1 | a0001c0002t0005g0350 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1223+1907C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719283 | |||||||
| chr7:129719294 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1223+1918G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719294 | |||||||
| chr7:129719411 | C | T | 4 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | NA18965.hp1 NA19058.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1223+2035C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719411 | |||||||
| chr7:129719497 | A | AAC | 17 | a0001c0002t0001g0345 a0001c0002t0001g0359 a0001c0002t0001g0360 others(14): Show |
17 | HG01074.hp1 HG01109.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1223+2167_1223+216 others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | A | AACAC | 18 | a0001c0001t0001g0126 a0001c0001t0013g0121 a0001c0002t0001g0361 others(15): Show |
18 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(15): Show |
intron_variant | MODIFIER | c.1223+2165_1223+216 others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | A | AACACAC | 7 | a0001c0001t0002g0154 a0001c0002t0001g0227 a0001c0002t0001g0382 others(4): Show |
7 | HG00323.hp1 HG01070.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1223+2163_1223+216 others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | A | AACACACA others(1): Show |
12 | a0001c0001t0002g0150 a0001c0001t0002g0153 a0001c0002t0003g0236 others(9): Show |
12 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1223+2161_1223+216 others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | A | AACACACA others(3): Show |
9 | a0001c0001t0008g0112 a0001c0002t0001g0349 a0001c0002t0003g0242 others(6): Show |
9 | HG00140.hp1 HG01934.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1223+2159_1223+216 others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | A | AACACACA others(5): Show |
17 | a0001c0001t0002g0158 a0001c0001t0008g0128 a0001c0002t0003g0229 others(14): Show |
17 | HG00639.hp2 HG01123.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1223+2157_1223+216 others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | A | AACACACA others(7): Show |
7 | a0001c0001t0002g0145 a0001c0001t0002g0155 a0001c0001t0008g0110 others(4): Show |
7 | HG00323.hp2 HG00558.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1223+2155_1223+216 others(18): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | A | AACACACA others(9): Show |
5 | a0001c0002t0003g0239 a0001c0002t0003g0246 a0001c0002t0003g0249 others(2): Show |
5 | HG01257.hp1 HG04228.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1223+2153_1223+216 others(20): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | A | AACACACA others(11): Show |
4 | a0001c0001t0002g0149 a0001c0001t0003g0183 a0001c0002t0003g0228 others(1): Show |
4 | HG01255.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223+2151_1223+216 others(22): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | A | ACACACAC others(4): Show |
1 | a0001c0001t0008g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1223+2121_1223+212 others(15): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719497 | |||||||
| chr7:129719497 | A | ACACACAC others(8): Show |
2 | a0001c0002t0003g0237 a0001c0002t0004g0335 |
2 | HG01993.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1223+2121_1223+212 others(19): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719497 | |||||||
| chr7:129719497 | AAC | A | 5 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0002t0001g0164 others(2): Show |
5 | HG02074.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1223+2167_1223+216 others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | AACACACA others(1): Show |
A | 5 | a0001c0002t0001g0366 a0001c0002t0001g0367 a0001c0002t0001g0372 others(2): Show |
5 | HG01975.hp1 HG01981.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1223+2161_1223+216 others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | AACACACA others(3): Show |
A | 4 | a0001c0002t0001g0223 a0001c0002t0001g0224 a0001c0002t0001g0225 others(1): Show |
4 | HG03491.hp2 HG03492.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223+2159_1223+216 others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | AACACACA others(5): Show |
A | 1 | a0001c0002t0001g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1223+2157_1223+216 others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | AACACACA others(7): Show |
A | 7 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
7 | HG00558.hp2 HG01361.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1223+2155_1223+216 others(18): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | AACACACA others(9): Show |
A | 10 | a0001c0001t0001g0179 a0001c0001t0001g0210 a0001c0001t0001g0213 others(7): Show |
10 | HG00621.hp2 HG01516.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.1223+2153_1223+216 others(20): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719497 | AACACACA others(11): Show |
A | 229 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(226): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1223+2151_1223+216 others(22): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719497 | ||||||
| chr7:129719543 | C | CACACACA others(3): Show |
1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1223+2168_1223+216 others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719543 | ||||||
| chr7:129719655 | C | CG | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1223+2280dupG | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129719655 | ||||||
| chr7:129719659 | T | C | 1 | a0001c0002t0001g0384 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1223+2283T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719659 | |||||||
| chr7:129719896 | A | T | 166 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(163): Show |
166 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.1223+2520A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719896 | |||||||
| chr7:129719897 | G | A | 1 | a0001c0002t0001g0225 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1223+2521G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129719897 | |||||||
| chr7:129720176 | A | T | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1223+2800A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129720176 | |||||||
| chr7:129720261 | A | G | 1 | a0001c0002t0005g0279 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1223+2885A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129720261 | |||||||
| chr7:129720361 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1223+2985G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129720361 | |||||||
| chr7:129720480 | C | T | 1 | a0001c0002t0004g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1223+3104C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129720480 | |||||||
| chr7:129720510 | C | T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(13): Show |
16 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1223+3134C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129720510 | |||||||
| chr7:129720663 | G | A | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1223+3287G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129720663 | |||||||
| chr7:129720758 | T | G | 2 | a0001c0001t0009g0025 a0001c0001t0009g0135 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1223+3382T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129720758 | |||||||
| chr7:129720939 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1223+3563C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129720939 | |||||||
| chr7:129720992 | A | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1223+3616A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129720992 | |||||||
| chr7:129721252 | T | G | 2 | a0001c0001t0007g0086 a0001c0001t0007g0087 |
2 | NA18984.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1223+3876T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129721252 | |||||||
| chr7:129721275 | G | A | 7 | a0001c0001t0002g0062 a0001c0001t0002g0080 a0001c0001t0002g0081 others(4): Show |
7 | HG00438.hp2 NA18944.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1223+3899G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129721275 | |||||||
| chr7:129721374 | T | C | 314 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1223+3998T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129721374 | |||||||
| chr7:129721480 | C | CT | 10 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(7): Show |
10 | HG00621.hp1 HG01099.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.1223+4120dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129721480 | ||||||
| chr7:129721593 | T | G | 1 | a0001c0002t0005g0296 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1223+4217T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129721593 | |||||||
| chr7:129721599 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1223+4223G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129721599 | |||||||
| chr7:129721606 | C | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1223+4230C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129721606 | |||||||
| chr7:129721717 | G | A | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1223+4341G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129721717 | |||||||
| chr7:129721727 | C | T | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1223+4351C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129721727 | |||||||
| chr7:129721858 | G | A | 128 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1223+4482G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129721858 | |||||||
| chr7:129722146 | G | A | 1 | a0001c0002t0004g0256 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1223+4770G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722146 | |||||||
| chr7:129722208 | A | G | 1 | a0001c0002t0004g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1223+4832A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722208 | |||||||
| chr7:129722248 | G | A | 2 | a0001c0002t0005g0280 a0001c0002t0005g0327 |
2 | HG01167.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1223+4872G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722248 | |||||||
| chr7:129722323 | G | A | 1 | a0001c0002t0005g0308 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1224-4918G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722323 | |||||||
| chr7:129722379 | G | A | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1224-4862G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722379 | |||||||
| chr7:129722386 | C | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(6): Show |
9 | HG01167.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1224-4855C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722386 | |||||||
| chr7:129722387 | G | A | 128 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1224-4854G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722387 | |||||||
| chr7:129722544 | G | T | 6 | a0001c0002t0004g0230 a0001c0002t0004g0292 a0001c0002t0004g0295 others(3): Show |
6 | HG02027.hp2 HG03831.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1224-4697G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722544 | |||||||
| chr7:129722774 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1224-4467C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722774 | |||||||
| chr7:129722823 | G | A | 1 | a0001c0002t0004g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1224-4418G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722823 | |||||||
| chr7:129722825 | T | G | 23 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(20): Show |
23 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1224-4416T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722825 | |||||||
| chr7:129722848 | T | C | 3 | a0001c0002t0004g0324 a0001c0002t0004g0325 a0001c0002t0004g0326 |
3 | NA18943.hp2 NA18947.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1224-4393T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722848 | |||||||
| chr7:129722877 | G | T | 1 | a0001c0002t0001g0377 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1224-4364G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129722877 | |||||||
| chr7:129723427 | G | C | 1 | a0001c0002t0005g0303 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1224-3814G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129723427 | |||||||
| chr7:129723443 | C | CA | 10 | a0001c0001t0001g0170 a0001c0001t0001g0203 a0001c0001t0001g0204 others(7): Show |
10 | HG02135.hp1 HG03688.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224-3782dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129723443 | ||||||
| chr7:129723443 | CA | C | 24 | a0001c0001t0001g0175 a0001c0001t0002g0085 a0001c0001t0007g0086 others(21): Show |
24 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1224-3782delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 129723443 | ||||||
| chr7:129723459 | A | T | 3 | a0001c0001t0002g0093 a0001c0002t0001g0365 a0001c0002t0001g0379 |
3 | HG01109.hp1 HG03831.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1224-3782A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129723459 | |||||||
| chr7:129723460 | T | A | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(8): Show |
11 | HG01433.hp2 HG02055.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1224-3781T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129723460 | |||||||
| chr7:129723652 | C | T | 1 | a0001c0002t0001g0361 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1224-3589C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129723652 | |||||||
| chr7:129723929 | T | C | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1224-3312T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129723929 | |||||||
| chr7:129724077 | C | T | 50 | a0001c0001t0003g0183 a0001c0001t0013g0121 a0001c0002t0003g0228 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1224-3164C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129724077 | |||||||
| chr7:129724344 | C | G | 230 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(227): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1224-2897C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129724344 | |||||||
| chr7:129724389 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1224-2852G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129724389 | |||||||
| chr7:129724534 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1224-2707A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129724534 | |||||||
| chr7:129724645 | G | C | 1 | a0001c0002t0003g0352 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1224-2596G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129724645 | |||||||
| chr7:129724832 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1224-2409T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129724832 | |||||||
| chr7:129725000 | C | T | 13 | a0001c0001t0001g0184 a0001c0001t0001g0198 a0001c0001t0001g0199 others(10): Show |
13 | HG00673.hp2 HG01361.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1224-2241C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129725000 | |||||||
| chr7:129725050 | A | T | 56 | a0001c0001t0003g0183 a0001c0001t0013g0121 a0001c0002t0003g0228 others(53): Show |
56 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1224-2191A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129725050 | |||||||
| chr7:129725397 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1224-1844G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129725397 | |||||||
| chr7:129725404 | T | C | 315 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(312): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.1224-1837T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129725404 | |||||||
| chr7:129725508 | G | A | 1 | a0001c0002t0001g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1224-1733G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129725508 | |||||||
| chr7:129725624 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1224-1617G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129725624 | |||||||
| chr7:129725713 | C | T | 1 | a0001c0003t0001g0014 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1224-1528C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129725713 | |||||||
| chr7:129725874 | C | T | 1 | a0001c0002t0003g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1224-1367C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129725874 | |||||||
| chr7:129726214 | A | C | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1224-1027A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129726214 | |||||||
| chr7:129726312 | A | G | 1 | a0001c0001t0007g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1224-929A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129726312 | |||||||
| chr7:129726517 | G | A | 13 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0036 others(10): Show |
13 | HG00438.hp2 HG01123.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1224-724G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129726517 | |||||||
| chr7:129726761 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1224-480C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129726761 | |||||||
| chr7:129726907 | C | T | 1 | a0001c0002t0005g0350 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224-334C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129726907 | |||||||
| chr7:129726961 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1224-280A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129726961 | |||||||
| chr7:129726994 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1224-247C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 9/10 | chr7 | 129726994 | |||||||
| chr7:129727406 | T | C | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1348+41T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129727406 | |||||||
| chr7:129727588 | T | C | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348+223T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129727588 | |||||||
| chr7:129727689 | C | T | 4 | a0001c0001t0009g0135 a0001c0002t0001g0340 a0001c0002t0001g0341 others(1): Show |
4 | HG02145.hp1 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1348+324C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129727689 | |||||||
| chr7:129727749 | A | T | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1348+384A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129727749 | |||||||
| chr7:129727750 | T | C | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1348+385T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129727750 | |||||||
| chr7:129727953 | T | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | HG00438.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1348+588T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129727953 | |||||||
| chr7:129728245 | C | T | 1 | a0001c0003t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1348+880C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129728245 | |||||||
| chr7:129728426 | G | A | 102 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(99): Show |
102 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1348+1061G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129728426 | |||||||
| chr7:129728468 | C | CA | 98 | a0001c0001t0001g0126 a0001c0001t0002g0030 a0001c0001t0002g0031 others(95): Show |
98 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1348+1129dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129728468 | ||||||
| chr7:129728468 | C | CAA | 39 | a0001c0001t0001g0118 a0001c0001t0001g0136 a0001c0001t0001g0140 others(36): Show |
39 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.1348+1128_1348+112 others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129728468 | ||||||
| chr7:129728468 | C | CAAA | 9 | a0001c0001t0001g0024 a0001c0001t0001g0123 a0001c0001t0001g0127 others(6): Show |
9 | HG01167.hp2 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1348+1127_1348+112 others(7): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129728468 | ||||||
| chr7:129728468 | CAAAAAAA others(8): Show |
C | 7 | a0001c0001t0001g0171 a0001c0001t0001g0202 a0001c0001t0001g0203 others(4): Show |
7 | HG01070.hp2 HG04228.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348+1115_1348+112 others(19): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129728468 | ||||||
| chr7:129728468 | CAAAAAAA others(9): Show |
C | 121 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(118): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1348+1114_1348+112 others(20): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129728468 | ||||||
| chr7:129728494 | A | C | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1348+1129A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129728494 | |||||||
| chr7:129728496 | C | G | 1 | a0001c0002t0005g0333 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1348+1131C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129728496 | |||||||
| chr7:129728650 | G | A | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+1285G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129728650 | |||||||
| chr7:129728772 | G | T | 128 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1348+1407G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129728772 | |||||||
| chr7:129729234 | A | AG | 314 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1348+1869_1348+187 others(5): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729234 | |||||||
| chr7:129729235 | A | G | 314 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1348+1870A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729235 | |||||||
| chr7:129729316 | G | T | 1 | a0001c0001t0002g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1348+1951G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729316 | |||||||
| chr7:129729317 | A | T | 1 | a0001c0001t0002g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1348+1952A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729317 | |||||||
| chr7:129729338 | T | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0208 |
2 | HG01361.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1348+1973T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729338 | |||||||
| chr7:129729512 | A | C | 128 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1348+2147A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729512 | |||||||
| chr7:129729597 | T | C | 1 | a0001c0001t0002g0107 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1348+2232T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729597 | |||||||
| chr7:129729701 | A | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348+2336A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729701 | |||||||
| chr7:129729722 | A | G | 4 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0155 others(1): Show |
4 | HG01243.hp2 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+2357A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729722 | |||||||
| chr7:129729723 | C | T | 1 | a0001c0001t0002g0092 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1348+2358C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729723 | |||||||
| chr7:129729837 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1348+2472G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729837 | |||||||
| chr7:129729950 | G | A | 5 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0036 others(2): Show |
5 | HG01123.hp1 HG01255.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348+2585G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129729950 | |||||||
| chr7:129730177 | A | T | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348+2812A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129730177 | |||||||
| chr7:129730258 | C | T | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1348+2893C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129730258 | |||||||
| chr7:129730667 | T | C | 61 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1348+3302T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129730667 | |||||||
| chr7:129730833 | C | T | 1 | a0001c0002t0004g0323 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1348+3468C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129730833 | |||||||
| chr7:129730976 | C | CA | 22 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0171 others(19): Show |
22 | HG00438.hp2 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1348+3625dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129730976 | ||||||
| chr7:129731159 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1348+3794G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731159 | |||||||
| chr7:129731172 | C | A | 102 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(99): Show |
102 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1348+3807C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731172 | |||||||
| chr7:129731241 | G | A | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1348+3876G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731241 | |||||||
| chr7:129731266 | G | A | 2 | a0001c0002t0003g0250 a0001c0002t0003g0251 |
2 | NA19070.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1348+3901G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731266 | |||||||
| chr7:129731271 | GA | G | 159 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0027 others(156): Show |
159 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1348+3923delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129731271 | ||||||
| chr7:129731291 | T | C | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1348+3926T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731291 | |||||||
| chr7:129731294 | T | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1348+3929T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731294 | |||||||
| chr7:129731397 | G | C | 343 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(340): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.1348+4032G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731397 | |||||||
| chr7:129731550 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1348+4185T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731550 | |||||||
| chr7:129731611 | C | CTTGT | 55 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(52): Show |
55 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1348+4277_1348+428 others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129731611 | ||||||
| chr7:129731611 | C | CTTGTTTG others(1): Show |
75 | a0001c0001t0001g0207 a0001c0001t0002g0022 a0001c0001t0002g0023 others(72): Show |
75 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1348+4273_1348+428 others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129731611 | ||||||
| chr7:129731611 | C | CTTGTTTG others(5): Show |
5 | a0001c0001t0002g0026 a0001c0001t0002g0091 a0001c0001t0002g0130 others(2): Show |
5 | HG01243.hp1 HG01516.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1348+4269_1348+428 others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129731611 | ||||||
| chr7:129731611 | CTTGT | C | 3 | a0001c0001t0017g0139 a0001c0002t0001g0342 a0001c0002t0001g0384 |
3 | HG01943.hp2 HG02135.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1348+4277_1348+428 others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129731611 | ||||||
| chr7:129731611 | CTTGTTTG others(1): Show |
C | 65 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(62): Show |
65 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1348+4273_1348+428 others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129731611 | ||||||
| chr7:129731614 | G | GTTTGTTT others(2): Show |
4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+4252_1348+426 others(13): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129731614 | ||||||
| chr7:129731673 | G | C | 61 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1348+4308G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731673 | |||||||
| chr7:129731790 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1348+4425T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731790 | |||||||
| chr7:129731909 | G | A | 129 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(126): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1348+4544G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731909 | |||||||
| chr7:129731965 | A | G | 1 | a0001c0003t0001g0008 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1348+4600A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129731965 | |||||||
| chr7:129732084 | A | G | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+4719A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732084 | |||||||
| chr7:129732139 | C | G | 1 | a0001c0002t0001g0340 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1348+4774C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732139 | |||||||
| chr7:129732245 | G | C | 347 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(344): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.1348+4880G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732245 | |||||||
| chr7:129732389 | G | GT | 4 | a0001c0001t0001g0203 a0001c0001t0002g0071 a0001c0002t0001g0377 others(1): Show |
4 | HG02300.hp2 NA18949.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+5031dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129732389 | ||||||
| chr7:129732433 | A | G | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1348+5068A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732433 | |||||||
| chr7:129732458 | C | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348+5093C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732458 | |||||||
| chr7:129732535 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1348+5170A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732535 | |||||||
| chr7:129732541 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1348+5176A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732541 | |||||||
| chr7:129732575 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1348+5210T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732575 | |||||||
| chr7:129732590 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1348+5225T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732590 | |||||||
| chr7:129732598 | T | TTTTG | 340 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(337): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.1348+5249_1348+525 others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129732598 | ||||||
| chr7:129732598 | T | TTTTGTTT others(1): Show |
6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348+5245_1348+525 others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129732598 | ||||||
| chr7:129732656 | G | A | 13 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0036 others(10): Show |
13 | HG00438.hp2 HG01123.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1348+5291G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732656 | |||||||
| chr7:129732694 | C | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348+5329C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732694 | |||||||
| chr7:129732728 | G | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1348+5363G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732728 | |||||||
| chr7:129732769 | T | A | 314 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1348+5404T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732769 | |||||||
| chr7:129732927 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1348+5562C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732927 | |||||||
| chr7:129732933 | T | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1348+5568T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129732933 | |||||||
| chr7:129733042 | G | C | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348+5677G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733042 | |||||||
| chr7:129733061 | A | ACT | 381 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(378): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1348+5697_1348+569 others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129733061 | ||||||
| chr7:129733087 | T | C | 1 | a0001c0001t0007g0108 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1348+5722T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733087 | |||||||
| chr7:129733149 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1348+5784T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733149 | |||||||
| chr7:129733195 | C | T | 4 | a0001c0001t0001g0136 a0001c0002t0001g0164 a0001c0002t0001g0349 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+5830C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733195 | |||||||
| chr7:129733328 | G | A | 186 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(183): Show |
186 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.1348+5963G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733328 | |||||||
| chr7:129733329 | C | T | 1 | a0001c0002t0005g0328 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1348+5964C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733329 | |||||||
| chr7:129733344 | G | A | 128 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1348+5979G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733344 | |||||||
| chr7:129733424 | G | A | 1 | a0001c0002t0003g0334 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1348+6059G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733424 | |||||||
| chr7:129733465 | C | CA | 131 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(128): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1348+6112dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129733465 | ||||||
| chr7:129733465 | C | CAA | 54 | a0001c0001t0001g0178 a0001c0001t0013g0121 a0001c0002t0003g0228 others(51): Show |
54 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1348+6111_1348+611 others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129733465 | ||||||
| chr7:129733567 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1348+6202T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733567 | |||||||
| chr7:129733579 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1348+6214T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733579 | |||||||
| chr7:129733657 | T | C | 1 | a0001c0002t0003g0262 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1348+6292T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733657 | |||||||
| chr7:129733672 | A | T | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1348+6307A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733672 | |||||||
| chr7:129733827 | C | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0163 |
2 | HG01099.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1348+6462C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733827 | |||||||
| chr7:129733869 | T | C | 7 | a0001c0002t0005g0278 a0001c0002t0005g0294 a0001c0002t0005g0296 others(4): Show |
7 | HG01346.hp2 NA18939.hp1 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.1348+6504T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733869 | |||||||
| chr7:129733977 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1348+6612C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733977 | |||||||
| chr7:129733983 | G | A | 347 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(344): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.1348+6618G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129733983 | |||||||
| chr7:129734138 | G | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1348+6773G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734138 | |||||||
| chr7:129734366 | T | C | 61 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1348+7001T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734366 | |||||||
| chr7:129734529 | C | A | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1348+7164C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734529 | |||||||
| chr7:129734530 | A | C | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1348+7165A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734530 | |||||||
| chr7:129734532 | C | A | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1348+7167C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734532 | |||||||
| chr7:129734541 | G | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1348+7176G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734541 | |||||||
| chr7:129734581 | C | T | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348+7216C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734581 | |||||||
| chr7:129734587 | C | A | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1348+7222C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734587 | |||||||
| chr7:129734663 | C | G | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1348+7298C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734663 | |||||||
| chr7:129734665 | G | T | 1 | a0001c0002t0003g0268 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1348+7300G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734665 | |||||||
| chr7:129734715 | G | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(7): Show |
10 | HG01167.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1348+7350G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734715 | |||||||
| chr7:129734817 | A | G | 314 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1348+7452A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129734817 | |||||||
| chr7:129735285 | A | C | 2 | a0001c0002t0004g0299 a0001c0002t0004g0306 |
2 | HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1348+7920A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735285 | |||||||
| chr7:129735303 | G | A | 5 | a0001c0001t0004g0177 a0001c0002t0004g0233 a0001c0002t0004g0234 others(2): Show |
5 | HG00140.hp2 HG00280.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348+7938G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735303 | |||||||
| chr7:129735307 | G | A | 1 | a0001c0002t0005g0350 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1348+7942G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735307 | |||||||
| chr7:129735363 | A | C | 314 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1348+7998A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735363 | |||||||
| chr7:129735391 | G | T | 102 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(99): Show |
102 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1348+8026G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735391 | |||||||
| chr7:129735612 | TTCGCAAG others(107): Show |
T | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8248_1348+836 others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735612 | |||||||
| chr7:129735712 | C | G | 2 | a0001c0002t0003g0242 a0001c0002t0003g0243 |
2 | HG01934.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1348+8347C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735712 | |||||||
| chr7:129735727 | C | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8362C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735727 | |||||||
| chr7:129735728 | A | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8363A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735728 | |||||||
| chr7:129735744 | G | C | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8379G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735744 | |||||||
| chr7:129735746 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1348+8381C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735746 | |||||||
| chr7:129735780 | A | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8415A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735780 | |||||||
| chr7:129735782 | A | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8417A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735782 | |||||||
| chr7:129735783 | T | C | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8418T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735783 | |||||||
| chr7:129735805 | G | A | 2 | a0001c0002t0001g0340 a0001c0002t0001g0341 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1348+8440G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735805 | |||||||
| chr7:129735815 | T | C | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8450T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735815 | |||||||
| chr7:129735817 | A | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8452A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735817 | |||||||
| chr7:129735822 | C | A | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8457C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735822 | |||||||
| chr7:129735857 | T | A | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8492T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735857 | |||||||
| chr7:129735865 | A | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8500A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735865 | |||||||
| chr7:129735866 | T | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8501T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735866 | |||||||
| chr7:129735871 | G | A | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8506G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735871 | |||||||
| chr7:129735877 | A | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8512A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735877 | |||||||
| chr7:129735881 | A | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8516A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735881 | |||||||
| chr7:129735932 | T | C | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8567T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735932 | |||||||
| chr7:129735939 | T | C | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8574T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735939 | |||||||
| chr7:129735952 | A | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8587A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735952 | |||||||
| chr7:129735957 | T | G | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8592T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735957 | |||||||
| chr7:129735969 | G | C | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8604G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735969 | |||||||
| chr7:129735981 | T | C | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+8616T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735981 | |||||||
| chr7:129735998 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1348+8633G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129735998 | |||||||
| chr7:129736039 | A | T | 2 | a0001c0002t0001g0340 a0001c0002t0001g0341 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1348+8674A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129736039 | |||||||
| chr7:129736172 | A | G | 2 | a0001c0002t0001g0359 a0001c0002t0001g0360 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1348+8807A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129736172 | |||||||
| chr7:129736274 | A | AT | 8 | a0001c0001t0001g0174 a0001c0001t0001g0201 a0001c0001t0001g0204 others(5): Show |
8 | HG00140.hp1 HG00673.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348+8932dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129736274 | ||||||
| chr7:129736274 | AT | A | 105 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(102): Show |
105 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1348+8932delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129736274 | ||||||
| chr7:129736274 | ATT | A | 204 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(201): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1348+8931_1348+893 others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129736274 | ||||||
| chr7:129736274 | ATTT | A | 6 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0002g0073 others(3): Show |
6 | HG00280.hp1 HG00323.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.1348+8930_1348+893 others(7): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129736274 | ||||||
| chr7:129736354 | T | C | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1348+8989T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129736354 | |||||||
| chr7:129736441 | G | A | 1 | a0001c0002t0003g0247 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1348+9076G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129736441 | |||||||
| chr7:129736498 | C | T | 3 | a0001c0002t0001g0370 a0001c0002t0011g0371 a0001c0004t0001g0369 |
3 | HG00140.hp1 HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1348+9133C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129736498 | |||||||
| chr7:129736610 | A | AT | 151 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1348+9254dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129736610 | ||||||
| chr7:129736631 | CT | C | 313 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(310): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1348+9278delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129736631 | ||||||
| chr7:129736653 | C | T | 5 | a0001c0002t0003g0266 a0001c0002t0003g0267 a0001c0002t0003g0268 others(2): Show |
5 | NA18953.hp1 NA18959.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348+9288C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129736653 | |||||||
| chr7:129736680 | T | G | 3 | a0001c0002t0005g0294 a0001c0002t0005g0296 a0001c0002t0005g0339 |
3 | HG01346.hp2 NA19074.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1348+9315T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129736680 | |||||||
| chr7:129736984 | A | G | 1 | a0001c0002t0004g0321 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1348+9619A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129736984 | |||||||
| chr7:129737278 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1348+9913A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129737278 | |||||||
| chr7:129737383 | G | T | 1 | a0001c0002t0006g0354 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1348+10018G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129737383 | |||||||
| chr7:129737426 | A | G | 2 | a0001c0002t0003g0288 a0001c0002t0003g0334 |
2 | HG01123.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1348+10061A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129737426 | |||||||
| chr7:129737506 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0215 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1348+10141A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129737506 | |||||||
| chr7:129737594 | TC | T | 162 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(159): Show |
162 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1348+10232delC | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129737594 | ||||||
| chr7:129737616 | G | A | 1 | a0001c0002t0003g0264 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1348+10251G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129737616 | |||||||
| chr7:129737865 | T | C | 1 | a0001c0001t0003g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1348+10500T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129737865 | |||||||
| chr7:129737887 | C | G | 14 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(11): Show |
14 | HG01099.hp2 HG01167.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1348+10522C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129737887 | |||||||
| chr7:129737895 | C | T | 4 | a0001c0001t0001g0136 a0001c0002t0001g0164 a0001c0002t0001g0349 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+10530C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129737895 | |||||||
| chr7:129738349 | C | T | 343 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(340): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.1348+10984C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738349 | |||||||
| chr7:129738458 | C | G | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | NA18945.hp2 NA18963.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348+11093C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738458 | |||||||
| chr7:129738557 | C | T | 31 | a0001c0001t0004g0177 a0001c0002t0004g0138 a0001c0002t0004g0230 others(28): Show |
31 | HG00140.hp2 HG00280.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1348+11192C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738557 | |||||||
| chr7:129738728 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1348+11363C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738728 | |||||||
| chr7:129738800 | C | T | 102 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(99): Show |
102 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1348+11435C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738800 | |||||||
| chr7:129738802 | G | C | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1348+11437G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738802 | |||||||
| chr7:129738911 | T | A | 1 | a0001c0002t0001g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1348+11546T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738911 | |||||||
| chr7:129738912 | A | G | 1 | a0001c0002t0001g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1348+11547A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738912 | |||||||
| chr7:129738913 | G | C | 1 | a0001c0002t0001g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1348+11548G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738913 | |||||||
| chr7:129738990 | T | G | 1 | a0001c0002t0001g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1348+11625T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738990 | |||||||
| chr7:129738992 | G | T | 1 | a0001c0002t0001g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1348+11627G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129738992 | |||||||
| chr7:129739026 | A | T | 1 | a0001c0002t0001g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1348+11661A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129739026 | |||||||
| chr7:129739092 | A | T | 1 | a0001c0002t0001g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1348+11727A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129739092 | |||||||
| chr7:129739093 | T | A | 1 | a0001c0002t0001g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1348+11728T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129739093 | |||||||
| chr7:129739173 | T | C | 60 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(57): Show |
60 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1348+11808T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129739173 | |||||||
| chr7:129739181 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1348+11816C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129739181 | |||||||
| chr7:129739425 | C | T | 4 | a0001c0002t0004g0230 a0001c0002t0004g0292 a0001c0002t0004g0295 others(1): Show |
4 | HG03831.hp1 NA18975.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1348+12060C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129739425 | |||||||
| chr7:129739465 | G | T | 1 | a0001c0001t0002g0109 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1348+12100G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129739465 | |||||||
| chr7:129739541 | T | TA | 62 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(59): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1348+12192dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129739541 | ||||||
| chr7:129739541 | TA | T | 102 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(99): Show |
102 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1348+12192delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129739541 | ||||||
| chr7:129739961 | C | T | 64 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(61): Show |
64 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1348+12596C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129739961 | |||||||
| chr7:129740266 | T | C | 381 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(378): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1348+12901T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740266 | |||||||
| chr7:129740313 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1348+12948T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740313 | |||||||
| chr7:129740403 | T | C | 102 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(99): Show |
102 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1348+13038T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740403 | |||||||
| chr7:129740435 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348+13070G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740435 | |||||||
| chr7:129740467 | T | C | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348+13102T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740467 | |||||||
| chr7:129740579 | C | A | 4 | a0001c0002t0003g0352 a0001c0002t0005g0344 a0001c0002t0005g0350 others(1): Show |
4 | HG01433.hp2 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+13214C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740579 | |||||||
| chr7:129740581 | C | T | 102 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(99): Show |
102 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1348+13216C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740581 | |||||||
| chr7:129740585 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1348+13220G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740585 | |||||||
| chr7:129740621 | G | A | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1348+13256G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740621 | |||||||
| chr7:129740745 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1348+13380C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740745 | |||||||
| chr7:129740807 | G | T | 64 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(61): Show |
64 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1348+13442G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740807 | |||||||
| chr7:129740855 | A | T | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1348+13490A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740855 | |||||||
| chr7:129740981 | A | T | 1 | a0001c0002t0001g0364 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1348+13616A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129740981 | |||||||
| chr7:129741316 | C | G | 163 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(160): Show |
163 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1349-13702C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129741316 | |||||||
| chr7:129741701 | C | T | 2 | a0001c0002t0001g0359 a0001c0002t0001g0360 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1349-13317C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129741701 | |||||||
| chr7:129741801 | A | G | 1 | a0001c0001t0002g0104 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1349-13217A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129741801 | |||||||
| chr7:129741886 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1349-13132G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129741886 | |||||||
| chr7:129741920 | A | G | 1 | a0001c0001t0002g0156 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1349-13098A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129741920 | |||||||
| chr7:129742037 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1349-12981G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129742037 | |||||||
| chr7:129742113 | A | G | 348 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(345): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.1349-12905A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129742113 | |||||||
| chr7:129742275 | T | TA | 16 | a0001c0001t0001g0126 a0001c0001t0002g0021 a0001c0001t0002g0033 others(13): Show |
16 | HG00408.hp2 HG01106.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1349-12726dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129742275 | ||||||
| chr7:129742275 | T | TAAA | 20 | a0001c0003t0001g0001 a0001c0003t0001g0003 a0001c0003t0001g0004 others(17): Show |
20 | HG00099.hp1 HG00621.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1349-12728_1349-12 others(9): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129742275 | ||||||
| chr7:129742275 | TA | T | 110 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(107): Show |
110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1349-12726delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129742275 | ||||||
| chr7:129742275 | TAA | T | 7 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(4): Show |
7 | HG02055.hp2 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1349-12727_1349-12 others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129742275 | ||||||
| chr7:129742284 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1349-12734A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129742284 | |||||||
| chr7:129742292 | AC | A | 10 | a0001c0001t0002g0061 a0001c0001t0002g0109 a0001c0001t0007g0087 others(7): Show |
10 | HG00323.hp2 HG01256.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1349-12725delC | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129742292 | |||||||
| chr7:129742293 | C | A | 181 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(178): Show |
181 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1349-12725C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129742293 | |||||||
| chr7:129742295 | A | C | 1 | a0001c0001t0002g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1349-12723A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129742295 | |||||||
| chr7:129742332 | G | C | 1 | a0001c0002t0001g0345 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1349-12686G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129742332 | |||||||
| chr7:129742350 | C | CT | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-12667dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129742350 | ||||||
| chr7:129742994 | G | A | 8 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0147 others(5): Show |
8 | HG01361.hp2 HG02970.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1349-12024G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129742994 | |||||||
| chr7:129743136 | C | G | 1 | a0001c0002t0004g0326 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1349-11882C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129743136 | |||||||
| chr7:129743155 | G | T | 314 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(311): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1349-11863G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129743155 | |||||||
| chr7:129743160 | C | A | 1 | a0001c0003t0001g0008 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1349-11858C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129743160 | |||||||
| chr7:129743175 | TA | T | 239 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(236): Show |
239 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1349-11828delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129743175 | ||||||
| chr7:129743175 | TAA | T | 65 | a0001c0001t0001g0172 a0001c0001t0001g0180 a0001c0001t0001g0181 others(62): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1349-11829_1349-11 others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129743175 | ||||||
| chr7:129743199 | A | G | 1 | a0001c0002t0004g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1349-11819A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129743199 | |||||||
| chr7:129743762 | A | G | 1 | a0001c0001t0002g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1349-11256A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129743762 | |||||||
| chr7:129743952 | C | G | 61 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1349-11066C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129743952 | |||||||
| chr7:129744063 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1349-10955C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129744063 | |||||||
| chr7:129744130 | C | CT | 24 | a0001c0001t0001g0024 a0001c0001t0001g0173 a0001c0001t0001g0174 others(21): Show |
24 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1349-10868dupT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129744130 | ||||||
| chr7:129744130 | C | CTTT | 20 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(17): Show |
20 | HG00423.hp2 HG00621.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1349-10870_1349-10 others(9): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129744130 | ||||||
| chr7:129744598 | G | A | 102 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(99): Show |
102 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1349-10420G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129744598 | |||||||
| chr7:129744702 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1349-10316A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129744702 | |||||||
| chr7:129744746 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1349-10272G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129744746 | |||||||
| chr7:129744902 | AG | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-10115delG | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129744902 | |||||||
| chr7:129744936 | T | TGGGG | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-10080_1349-10 others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129744936 | ||||||
| chr7:129745003 | G | GA | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-10005dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129745003 | ||||||
| chr7:129745003 | GA | G | 61 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1349-10005delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129745003 | ||||||
| chr7:129745111 | T | C | 4 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0132 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1349-9907T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129745111 | |||||||
| chr7:129745202 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-9816G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129745202 | |||||||
| chr7:129745203 | A | C | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-9815A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129745203 | |||||||
| chr7:129745296 | T | C | 347 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(344): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.1349-9722T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129745296 | |||||||
| chr7:129745440 | A | C | 2 | a0001c0002t0005g0350 a0001c0002t0005g0353 |
2 | HG01433.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1349-9578A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129745440 | |||||||
| chr7:129745486 | TCCCCAAA others(7): Show |
T | 3 | a0001c0002t0001g0374 a0001c0002t0006g0380 a0001c0002t0006g0381 |
3 | HG00642.hp2 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1349-9529_1349-951 others(18): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129745486 | ||||||
| chr7:129745506 | A | AC | 122 | a0001c0001t0001g0178 a0001c0001t0001g0214 a0001c0001t0002g0149 others(119): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1349-9502dupC | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129745506 | ||||||
| chr7:129745506 | AC | A | 100 | a0001c0001t0001g0192 a0001c0001t0002g0021 a0001c0001t0002g0022 others(97): Show |
100 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1349-9502delC | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129745506 | ||||||
| chr7:129745508 | C | A | 4 | a0001c0001t0008g0110 a0001c0001t0008g0111 a0001c0001t0008g0112 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1349-9510C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129745508 | |||||||
| chr7:129745781 | T | C | 381 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(378): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1349-9237T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129745781 | |||||||
| chr7:129746317 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1349-8701T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129746317 | |||||||
| chr7:129746620 | T | C | 2 | a0001c0001t0002g0048 a0001c0001t0002g0054 |
2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1349-8398T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129746620 | |||||||
| chr7:129746713 | A | G | 4 | a0001c0002t0003g0352 a0001c0002t0005g0344 a0001c0002t0005g0350 others(1): Show |
4 | HG01433.hp2 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1349-8305A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129746713 | |||||||
| chr7:129746922 | C | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-8096C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129746922 | |||||||
| chr7:129747060 | A | T | 1 | a0001c0003t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1349-7958A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129747060 | |||||||
| chr7:129747478 | T | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-7540T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129747478 | |||||||
| chr7:129747529 | C | A | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1349-7489C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129747529 | |||||||
| chr7:129747540 | A | C | 151 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1349-7478A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129747540 | |||||||
| chr7:129747571 | A | C | 128 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1349-7447A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129747571 | |||||||
| chr7:129747608 | T | C | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1349-7410T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129747608 | |||||||
| chr7:129747885 | C | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1349-7133C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129747885 | |||||||
| chr7:129748019 | T | C | 4 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0155 others(1): Show |
4 | HG01243.hp2 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1349-6999T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129748019 | |||||||
| chr7:129748057 | C | T | 1 | a0001c0002t0004g0261 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1349-6961C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129748057 | |||||||
| chr7:129748132 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0073 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1349-6886G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129748132 | |||||||
| chr7:129748145 | C | T | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1349-6873C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129748145 | |||||||
| chr7:129748235 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1349-6783A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129748235 | |||||||
| chr7:129748274 | C | CA | 57 | a0001c0001t0001g0181 a0001c0001t0002g0146 a0001c0001t0004g0177 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1349-6722dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129748274 | ||||||
| chr7:129748274 | C | CAA | 57 | a0001c0001t0001g0168 a0001c0001t0001g0172 a0001c0001t0001g0175 others(54): Show |
57 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1349-6723_1349-672 others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129748274 | ||||||
| chr7:129748274 | C | CAAA | 148 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(145): Show |
148 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1349-6724_1349-672 others(7): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129748274 | ||||||
| chr7:129748274 | C | CAAAA | 23 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(20): Show |
23 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1349-6725_1349-672 others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129748274 | ||||||
| chr7:129748274 | CAAAAAAA others(2): Show |
C | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-6730_1349-672 others(13): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129748274 | ||||||
| chr7:129748274 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1349-6731_1349-672 others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129748274 | ||||||
| chr7:129748416 | G | A | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1349-6602G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129748416 | |||||||
| chr7:129748542 | A | C | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1349-6476A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129748542 | |||||||
| chr7:129748677 | TGATGG | T | 63 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(60): Show |
63 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1349-6330_1349-632 others(9): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129748677 | ||||||
| chr7:129748807 | T | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-6211T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129748807 | |||||||
| chr7:129748813 | A | C | 1 | a0001c0001t0002g0166 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1349-6205A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129748813 | |||||||
| chr7:129749012 | C | G | 2 | a0001c0002t0004g0316 a0001c0002t0004g0317 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1349-6006C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749012 | |||||||
| chr7:129749045 | G | T | 5 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
5 | HG02818.hp1 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1349-5973G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749045 | |||||||
| chr7:129749055 | A | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-5963A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749055 | |||||||
| chr7:129749307 | A | AGGGGGGG others(98): Show |
1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1349-5711_1349-571 others(109): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749307 | |||||||
| chr7:129749308 | A | G | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1349-5710A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749308 | |||||||
| chr7:129749309 | GTAAAGGA others(102): Show |
G | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1349-5708_1349-560 others(4): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749309 | |||||||
| chr7:129749414 | C | T | 6 | a0001c0002t0003g0282 a0001c0002t0003g0283 a0001c0002t0003g0284 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1349-5604C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749414 | |||||||
| chr7:129749432 | T | TA | 81 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1349-5571dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129749432 | ||||||
| chr7:129749432 | TA | T | 11 | a0001c0001t0001g0127 a0001c0001t0002g0028 a0001c0001t0002g0029 others(8): Show |
11 | HG00323.hp2 HG01070.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1349-5571delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129749432 | ||||||
| chr7:129749433 | A | T | 1 | a0001c0002t0003g0231 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1349-5585A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749433 | |||||||
| chr7:129749448 | T | A | 1 | a0001c0002t0001g0340 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1349-5570T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749448 | |||||||
| chr7:129749449 | A | T | 1 | a0001c0001t0006g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1349-5569A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749449 | |||||||
| chr7:129749824 | G | T | 1 | a0001c0002t0001g0379 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1349-5194G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749824 | |||||||
| chr7:129749880 | G | C | 4 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(1): Show |
4 | HG01261.hp2 HG01433.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1349-5138G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749880 | |||||||
| chr7:129749997 | G | A | 1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1349-5021G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129749997 | |||||||
| chr7:129750022 | T | A | 1 | a0001c0001t0002g0091 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1349-4996T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129750022 | |||||||
| chr7:129750073 | G | C | 33 | a0001c0001t0001g0126 a0001c0002t0001g0225 a0001c0002t0001g0226 others(30): Show |
33 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.1349-4945G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129750073 | |||||||
| chr7:129750344 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1349-4674G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129750344 | |||||||
| chr7:129750354 | G | A | 1 | a0001c0002t0005g0319 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1349-4664G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129750354 | |||||||
| chr7:129750505 | G | GTGGGA | 316 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(313): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.1349-4510_1349-450 others(9): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129750505 | ||||||
| chr7:129750543 | C | G | 17 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(14): Show |
17 | HG00423.hp2 HG00621.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1349-4475C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129750543 | |||||||
| chr7:129750561 | G | A | 64 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(61): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1349-4457G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129750561 | |||||||
| chr7:129750755 | T | G | 61 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.1349-4263T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129750755 | |||||||
| chr7:129750766 | G | T | 3 | a0001c0002t0001g0362 a0001c0002t0001g0376 a0001c0002t0014g0378 |
3 | HG00408.hp2 NA18954.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1349-4252G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129750766 | |||||||
| chr7:129750945 | T | G | 2 | a0001c0001t0007g0086 a0001c0001t0007g0087 |
2 | NA18984.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1349-4073T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129750945 | |||||||
| chr7:129751101 | G | A | 1 | a0001c0002t0003g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1349-3917G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129751101 | |||||||
| chr7:129751318 | T | C | 85 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(82): Show |
85 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1349-3700T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129751318 | |||||||
| chr7:129751414 | A | AGAT | 4 | a0001c0002t0003g0352 a0001c0002t0005g0344 a0001c0002t0005g0350 others(1): Show |
4 | HG01433.hp2 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1349-3603_1349-360 others(7): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129751414 | ||||||
| chr7:129751475 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1349-3543A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129751475 | |||||||
| chr7:129751672 | C | CTT | 64 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(61): Show |
64 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1349-3345_1349-334 others(6): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129751672 | ||||||
| chr7:129752029 | A | G | 64 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(61): Show |
64 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1349-2989A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752029 | |||||||
| chr7:129752041 | C | T | 102 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(99): Show |
102 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1349-2977C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752041 | |||||||
| chr7:129752150 | G | A | 1 | a0001c0002t0005g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1349-2868G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752150 | |||||||
| chr7:129752254 | A | G | 1 | a0001c0002t0005g0344 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1349-2764A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752254 | |||||||
| chr7:129752262 | C | T | 1 | a0001c0003t0001g0006 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1349-2756C>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752262 | |||||||
| chr7:129752372 | T | TG | 25 | a0001c0001t0002g0090 a0001c0002t0001g0384 a0001c0003t0001g0001 others(22): Show |
25 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1349-2640dupG | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129752372 | ||||||
| chr7:129752450 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1349-2568G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752450 | |||||||
| chr7:129752529 | ATGTT | A | 6 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0001t0002g0153 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1349-2486_1349-248 others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129752529 | ||||||
| chr7:129752662 | G | A | 1 | a0001c0001t0017g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1349-2356G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752662 | |||||||
| chr7:129752695 | A | C | 1 | a0001c0002t0004g0318 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1349-2323A>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752695 | |||||||
| chr7:129752729 | T | C | 23 | a0001c0003t0001g0001 a0001c0003t0001g0002 a0001c0003t0001g0003 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-2289T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752729 | |||||||
| chr7:129752758 | G | C | 4 | a0001c0002t0003g0352 a0001c0002t0005g0344 a0001c0002t0005g0350 others(1): Show |
4 | HG01433.hp2 HG02055.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1349-2260G>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752758 | |||||||
| chr7:129752840 | G | A | 162 | a0001c0001t0001g0159 a0001c0001t0002g0021 a0001c0001t0002g0022 others(159): Show |
162 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1349-2178G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752840 | |||||||
| chr7:129752918 | A | G | 1 | a0001c0002t0001g0340 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1349-2100A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129752918 | |||||||
| chr7:129753023 | A | T | 1 | a0001c0002t0002g0265 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1349-1995A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129753023 | |||||||
| chr7:129753136 | AT | A | 321 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(318): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1349-1874delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129753136 | ||||||
| chr7:129753150 | A | G | 1 | a0001c0002t0012g0311 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1349-1868A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129753150 | |||||||
| chr7:129753184 | T | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0215 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1349-1834T>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129753184 | |||||||
| chr7:129753322 | G | T | 58 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(55): Show |
58 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1349-1696G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129753322 | |||||||
| chr7:129753386 | G | A | 1 | a0001c0002t0003g0231 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1349-1632G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129753386 | |||||||
| chr7:129753402 | G | A | 3 | a0001c0002t0001g0340 a0001c0002t0001g0341 a0001c0002t0001g0342 |
3 | HG02886.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1349-1616G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129753402 | |||||||
| chr7:129753501 | A | G | 125 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(122): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1349-1517A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129753501 | |||||||
| chr7:129753532 | A | T | 60 | a0001c0001t0004g0177 a0001c0002t0001g0331 a0001c0002t0001g0332 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1349-1486A>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129753532 | |||||||
| chr7:129753726 | CT | C | 336 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(333): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.1349-1282delT | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129753726 | ||||||
| chr7:129753973 | CA | C | 23 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0003t0001g0001 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-1042delA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129753973 | ||||||
| chr7:129754170 | A | AT | 6 | a0001c0001t0002g0041 a0001c0001t0002g0043 a0001c0001t0002g0045 others(3): Show |
6 | HG00609.hp2 NA18943.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.1349-848_1349-847i others(3): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129754170 | |||||||
| chr7:129754213 | C | G | 1 | a0001c0002t0004g0373 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1349-805C>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129754213 | |||||||
| chr7:129754253 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1349-765G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129754253 | |||||||
| chr7:129754294 | C | CA | 23 | a0001c0002t0001g0331 a0001c0003t0001g0001 a0001c0003t0001g0002 others(20): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1349-710dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754294 | ||||||
| chr7:129754308 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1349-710A>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129754308 | |||||||
| chr7:129754396 | G | A | 243 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0023 others(240): Show |
243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1349-622G>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129754396 | |||||||
| chr7:129754400 | T | C | 349 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(346): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.1349-618T>C | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129754400 | |||||||
| chr7:129754420 | G | T | 1 | a0001c0001t0002g0082 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1349-598G>T | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129754420 | |||||||
| chr7:129754464 | T | TA | 24 | a0001c0002t0001g0331 a0001c0002t0001g0332 a0001c0003t0001g0001 others(21): Show |
24 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1349-535dupA | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAA | 13 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0123 others(10): Show |
13 | HG01167.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1349-540_1349-535d others(8): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA | 16 | a0001c0001t0002g0029 a0001c0001t0002g0034 a0001c0001t0002g0039 others(13): Show |
16 | HG02886.hp1 HG02965.hp2 HG02970.hp2 others(13): Show |
intron_variant | MODIFIER | c.1349-541_1349-535d others(9): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(1): Show |
84 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0026 others(81): Show |
84 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1349-542_1349-535d others(10): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(2): Show |
63 | a0001c0001t0001g0207 a0001c0001t0002g0021 a0001c0001t0002g0032 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1349-543_1349-535d others(11): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(3): Show |
28 | a0001c0002t0003g0231 a0001c0002t0003g0236 a0001c0002t0003g0244 others(25): Show |
28 | HG00280.hp1 HG00558.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.1349-544_1349-535d others(12): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(4): Show |
10 | a0001c0001t0002g0064 a0001c0002t0003g0242 a0001c0002t0003g0248 others(7): Show |
10 | HG00323.hp2 HG01934.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.1349-545_1349-535d others(13): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(5): Show |
24 | a0001c0001t0004g0177 a0001c0002t0004g0138 a0001c0002t0004g0230 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1349-546_1349-535d others(14): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(6): Show |
9 | a0001c0002t0004g0256 a0001c0002t0004g0293 a0001c0002t0004g0295 others(6): Show |
9 | HG01978.hp1 HG02027.hp2 HG04115.hp1 others(6): Show |
intron_variant | MODIFIER | c.1349-547_1349-535d others(15): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(7): Show |
1 | a0001c0001t0002g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1349-548_1349-535d others(16): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(8): Show |
6 | a0001c0001t0001g0206 a0001c0001t0002g0149 a0001c0001t0002g0153 others(3): Show |
6 | HG01496.hp2 HG01943.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1349-549_1349-535d others(17): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(9): Show |
19 | a0001c0001t0001g0136 a0001c0001t0001g0172 a0001c0001t0001g0195 others(16): Show |
19 | HG00597.hp2 HG00621.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1349-550_1349-535d others(18): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(10): Show |
29 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(26): Show |
29 | HG00544.hp2 HG00609.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1349-551_1349-535d others(19): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(11): Show |
9 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0169 others(6): Show |
9 | HG01071.hp1 HG01943.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1349-552_1349-535d others(20): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(12): Show |
2 | a0001c0001t0001g0170 a0001c0001t0001g0191 |
2 | HG02615.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1349-553_1349-535d others(21): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(13): Show |
1 | a0001c0002t0015g0351 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1349-535_1349-534i others(22): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(14): Show |
1 | a0001c0002t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1349-535_1349-534i others(23): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(18): Show |
1 | a0001c0001t0001g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1349-535_1349-534i others(27): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(19): Show |
1 | a0001c0001t0001g0187 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1349-535_1349-534i others(28): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(21): Show |
1 | a0001c0001t0001g0189 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1349-535_1349-534i others(30): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(23): Show |
1 | a0001c0001t0001g0188 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1349-535_1349-534i others(32): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754464 | T | TAAAAAAA others(24): Show |
1 | a0001c0001t0001g0186 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1349-535_1349-534i others(33): Show |
NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 129754464 | ||||||
| chr7:129754651 | T | G | 60 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0094 others(57): Show |
60 | HG00544.hp2 HG00621.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.1349-367T>G | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129754651 | |||||||
| chr7:129754905 | C | A | 1 | a0001c0001t0002g0021 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1349-113C>A | NRF1 | ENSG00000106459.15 | transcript | ENST00000393232.6 | protein_coding | 10/10 | chr7 | 129754905 |