Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84267 |
| ensemblid | ENSG00000165118.15 |
| hgncid | 28144 |
| symbol | QNG1 |
| name | Q-nucleotide N-glycosylase 1 |
| refseq_nuc | NM_032307.5 |
| refseq_prot | NP_115683.3 |
| ensembl_nuc | ENST00000376344.8 |
| ensembl_prot | ENSP00000365522.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 83938311 |
| end | 83956742 |
| strand | - |
| ver | v1.2 |
| region | chr9:83938311-83956742 |
| region5000 | chr9:83933311-83961742 |
| regionname0 | QNG1_chr9_83938311_83956742 |
| regionname5000 | QNG1_chr9_83933311_83961742 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 341 | 383 | 85 | 56 | 182 | 16 | 42 | 142 | QNG1_chr9_83933311_83961742 | QNG1 | MDGLL others(336): Show |
chr9 | 83933311 | 83961742 |
| a0002 | 0/0 | 341 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | MDGLL others(336): Show |
chr9 | 83933311 | 83961742 |
| a0003 | 0/0 | 341 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | MDGLL others(336): Show |
chr9 | 83933311 | 83961742 |
| a0004 | 0/0 | 341 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | MDGLL others(336): Show |
chr9 | 83933311 | 83961742 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1023 | 381 | 84 | 55 | 182 | 16 | 42 | QNG1_chr9_83933311_83961742 | QNG1 | ATGGA others(1018): Show |
chr9 | 83933311 | 83961742 | ||
| a0001c0006 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | ATGGA others(1018): Show |
chr9 | 83933311 | 83961742 | ||
| a0001c0007 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | ATGGA others(1018): Show |
chr9 | 83933311 | 83961742 | ||
| a0002c0002 | 0/0 | 1023 | 5 | 5 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | ATGGA others(1018): Show |
chr9 | 83933311 | 83961742 | ||
| a0003c0004 | 0/0 | 1023 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | ATGGA others(1018): Show |
chr9 | 83933311 | 83961742 | ||
| a0003c0005 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | ATGGA others(1018): Show |
chr9 | 83933311 | 83961742 | ||
| a0004c0003 | 0/0 | 1023 | 3 | 3 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | ATGGA others(1018): Show |
chr9 | 83933311 | 83961742 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2468 | 160 | 23 | 19 | 92 | 8 | 16 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0002 | 0/0 | 2467 | 102 | 32 | 18 | 38 | 3 | 11 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0003 | 0/0 | 2463 | 46 | 4 | 9 | 24 | 3 | 6 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2458): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0004 | 0/0 | 2469 | 13 | 0 | 0 | 12 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2464): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0006 | 0/0 | 2467 | 6 | 0 | 3 | 2 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0007 | 0/0 | 2470 | 6 | 6 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2465): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0008 | 0/0 | 2469 | 6 | 1 | 1 | 3 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2464): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0009 | 0/0 | 2467 | 5 | 5 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0010 | 0/0 | 2468 | 4 | 0 | 1 | 0 | 2 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0011 | 0/0 | 2467 | 3 | 3 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0012 | 0/0 | 2467 | 3 | 2 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0013 | 0/0 | 2470 | 3 | 2 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2465): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0015 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2465): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0016 | 0/0 | 2462 | 2 | 0 | 1 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2457): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0017 | 0/0 | 2468 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0018 | 0/0 | 2467 | 2 | 0 | 1 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0019 | 0/0 | 2471 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2466): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0020 | 0/0 | 2467 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0022 | 0/0 | 2468 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0023 | 0/0 | 2467 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0024 | 0/0 | 2467 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0026 | 0/0 | 2473 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2468): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0027 | 0/0 | 2467 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2462): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0028 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0029 | 0/0 | 2468 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0030 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0031 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0032 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0033 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0034 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0035 | 0/0 | 2468 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0001t0036 | 0/0 | 2468 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0006t0001 | 0/0 | 2468 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0001c0007t0015 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2465): Show |
chr9 | 83933311 | 83961742 |
| a0002c0002t0005 | 0/0 | 2470 | 5 | 5 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2465): Show |
chr9 | 83933311 | 83961742 |
| a0003c0004t0014 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0003c0004t0021 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2465): Show |
chr9 | 83933311 | 83961742 |
| a0003c0005t0014 | 0/0 | 2468 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2463): Show |
chr9 | 83933311 | 83961742 |
| a0004c0003t0005 | 0/0 | 2470 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2465): Show |
chr9 | 83933311 | 83961742 |
| a0004c0003t0025 | 0/0 | 2471 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | GGAAG others(2466): Show |
chr9 | 83933311 | 83961742 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/1 | 35 | 8 | 4 | 15 | 4 | 2 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0005 | 0/0 | 8 | 2 | 0 | 4 | 0 | 2 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0008 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0009 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0011 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0002 | 0/0 | 18 | 0 | 0 | 17 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0003 | 0/0 | 15 | 7 | 5 | 0 | 3 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0004 | 0/0 | 15 | 0 | 5 | 8 | 0 | 2 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0007 | 0/0 | 6 | 1 | 0 | 3 | 0 | 2 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0013 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0004g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0006g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0007g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0008g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0009g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0010g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0011g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0011g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0011g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0012g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0012g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0013g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0013g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0015g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0016g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0016g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0017g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0018g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0018g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0019g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0020g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0022g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0023g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0024g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0026g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0027g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0028g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0029g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0030g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0031g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0032g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0033g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0034g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0035g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0001t0036g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0006t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0001c0007t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0002c0002t0005g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0002c0002t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0003c0004t0014g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0003c0004t0021g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0003c0005t0014g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0004c0003t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0004c0003t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| a0004c0003t0025g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00609 | hp1 | a0001 | c0001 | t0013 | g0057 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0085 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00735 | hp2 | a0001 | c0001 | t0016 | g0118 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0219 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01256 | hp1 | a0001 | c0001 | t0018 | g0148 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0134 | EUR | IBS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0018 | EUR | IBS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0133 | EUR | IBS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0018 | EUR | IBS | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0055 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01943 | hp2 | a0001 | c0001 | t0029 | g0160 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01975 | hp2 | a0001 | c0006 | t0001 | g0188 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02004 | hp2 | a0001 | c0001 | t0010 | g0018 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02015 | hp2 | a0001 | c0001 | t0034 | g0185 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02055 | hp2 | a0002 | c0002 | t0005 | g0111 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02145 | hp2 | a0001 | c0001 | t0032 | g0202 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | CDX | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02257 | hp1 | a0003 | c0004 | t0014 | g0137 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02258 | hp2 | a0004 | c0003 | t0025 | g0130 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02280 | hp1 | a0004 | c0003 | t0005 | g0131 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0034 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02615 | hp2 | a0001 | c0007 | t0015 | g0138 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02622 | hp1 | a0002 | c0002 | t0005 | g0012 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0096 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0066 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02723 | hp1 | a0002 | c0002 | t0005 | g0012 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02738 | hp2 | a0001 | c0001 | t0008 | g0154 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02809 | hp1 | a0003 | c0004 | t0021 | g0136 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0135 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0097 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02895 | hp1 | a0001 | c0001 | t0017 | g0039 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02896 | hp1 | a0001 | c0001 | t0013 | g0026 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02897 | hp1 | a0001 | c0001 | t0017 | g0039 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0026 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0072 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0035 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02970 | hp2 | a0003 | c0005 | t0014 | g0049 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0035 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0167 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03017 | hp1 | a0001 | c0001 | t0036 | g0230 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0094 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03195 | hp1 | a0001 | c0001 | t0026 | g0110 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03195 | hp2 | a0001 | c0001 | t0027 | g0140 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03486 | hp2 | a0002 | c0002 | t0005 | g0012 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03516 | hp1 | a0004 | c0003 | t0005 | g0132 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0098 | AFR | ESN | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0108 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03654 | hp2 | a0001 | c0001 | t0024 | g0078 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | STU | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | STU | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03710 | hp1 | a0001 | c0001 | t0022 | g0077 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03831 | hp2 | a0001 | c0001 | t0016 | g0116 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0076 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03927 | hp1 | a0001 | c0001 | t0020 | g0048 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | STU | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | BEB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | STU | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG04204 | hp2 | a0001 | c0001 | t0010 | g0142 | SAS | STU | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | YRI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0093 | AFR | YRI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18944 | hp1 | a0001 | c0001 | t0019 | g0044 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18963 | hp1 | a0001 | c0001 | t0035 | g0229 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18970 | hp2 | a0001 | c0001 | t0019 | g0044 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18978 | hp2 | a0001 | c0001 | t0008 | g0146 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18982 | hp1 | a0001 | c0001 | t0018 | g0194 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19001 | hp2 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19011 | hp1 | a0001 | c0001 | t0028 | g0141 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0034 | AFR | LWK | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19059 | hp1 | a0001 | c0001 | t0031 | g0149 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19059 | hp2 | a0001 | c0001 | t0023 | g0064 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19077 | hp1 | a0001 | c0001 | t0008 | g0145 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19085 | hp1 | a0001 | c0001 | t0030 | g0156 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19085 | hp2 | a0001 | c0001 | t0033 | g0189 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0112 | AFR | YRI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA19240 | hp2 | a0002 | c0002 | t0005 | g0012 | AFR | YRI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ASW | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ASW | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0120 | EUR | TSI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | GIH | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | GIH | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01123 | hp1 | a0001 | c0001 | t0012 | g0084 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0139 | AMR | CLM | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0092 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | ACB | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | USA | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | LWK | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | QNG1_chr9_83933311_83961742 | QNG1 | chr9 | 83933311 | 83961742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:83944985 | T | C | 1 | a0002 | 5 | HG02055.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
missense_variant | MODERATE | c.602A>G | p.Lys201Arg | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/4 | 844/2468 | 602/1026 | 201/341 | chr9 | 83944985 | |||
| chr9:83955571 | G | T | 1 | a0003 | 3 | HG02257.hp1 HG02809.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.407C>A | p.Ser136Tyr | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/4 | 649/2468 | 407/1026 | 136/341 | chr9 | 83955571 | |||
| chr9:83955619 | G | C | 1 | a0004 | 3 | HG02258.hp2 HG02280.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.359C>G | p.Ser120Trp | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/4 | 601/2468 | 359/1026 | 120/341 | chr9 | 83955619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:83939697 | C | T | 1 | a0001c0006 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.840G>A | p.Gly280Gly | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 1082/2468 | 840/1026 | 280/341 | chr9 | 83939697 | |||
| chr9:83944798 | G | A | 1 | a0001c0007 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.789C>T | p.Leu263Leu | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/4 | 1031/2468 | 789/1026 | 263/341 | chr9 | 83944798 | |||
| chr9:83956207 | C | G | 1 | a0003c0005 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.294G>C | p.Gly98Gly | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/4 | 536/2468 | 294/1026 | 98/341 | chr9 | 83956207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:83938367 | C | A | 1 | a0001c0001t0031 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1144G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 1144 | chr9 | 83938367 | ||||||
| chr9:83938368 | A | C | 1 | a0001c0001t0031 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1143T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 1143 | chr9 | 83938368 | ||||||
| chr9:83938473 | G | A | 1 | a0001c0001t0012 | 3 | HG01123.hp1 HG02647.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1038C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 1038 | chr9 | 83938473 | ||||||
| chr9:83938481 | A | G | 5 | a0001c0001t0009 a0001c0001t0026 a0002c0002t0005 others(2): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1030T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 1030 | chr9 | 83938481 | ||||||
| chr9:83938643 | C | G | 1 | a0001c0001t0011 | 3 | HG02630.hp2 HG02886.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*868G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 868 | chr9 | 83938643 | ||||||
| chr9:83938673 | G | A | 1 | a0001c0001t0023 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*838C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 838 | chr9 | 83938673 | ||||||
| chr9:83938673 | G | GA | 5 | a0001c0001t0009 a0001c0001t0022 a0001c0001t0026 others(2): Show |
14 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*837_*838insT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 837 | chr9 | 83938673 | ||||||
| chr9:83938673 | G | GAA | 5 | a0001c0001t0007 a0001c0001t0015 a0001c0007t0015 others(2): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*837_*838insTT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 837 | chr9 | 83938673 | ||||||
| chr9:83938674 | G | A | 18 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(15): Show |
139 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*837C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 837 | chr9 | 83938674 | ||||||
| chr9:83938674 | G | GA | 3 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 |
65 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*836dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 836 | chr9 | 83938674 | ||||||
| chr9:83938675 | A | G | 1 | a0001c0001t0030 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 836 | chr9 | 83938675 | ||||||
| chr9:83938749 | AT | A | 11 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(8): Show |
124 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*761delA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 761 | chr9 | 83938749 | ||||||
| chr9:83938850 | C | A | 1 | a0001c0001t0032 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*661G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 661 | chr9 | 83938850 | ||||||
| chr9:83939057 | T | TTTG | 3 | a0001c0001t0013 a0001c0001t0019 a0001c0001t0026 |
6 | HG00609.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*451_*453dupCAA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 453 | chr9 | 83939057 | ||||||
| chr9:83939057 | TTTG | T | 1 | a0001c0001t0009 | 5 | HG02572.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*451_*453delCAA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 451 | chr9 | 83939057 | ||||||
| chr9:83939057 | TTTGTTG | T | 2 | a0001c0001t0003 a0001c0001t0016 |
48 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*448_*453delCAACAA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 448 | chr9 | 83939057 | ||||||
| chr9:83939079 | T | C | 1 | a0001c0001t0033 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 432 | chr9 | 83939079 | ||||||
| chr9:83939095 | C | CA | 5 | a0001c0001t0009 a0001c0001t0026 a0002c0002t0005 others(2): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*415dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 415 | chr9 | 83939095 | ||||||
| chr9:83939144 | C | T | 5 | a0001c0001t0015 a0001c0007t0015 a0003c0004t0014 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*367G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 367 | chr9 | 83939144 | ||||||
| chr9:83939223 | G | A | 1 | a0001c0001t0024 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*288C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 288 | chr9 | 83939223 | ||||||
| chr9:83939239 | A | G | 1 | a0001c0001t0029 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*272T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 272 | chr9 | 83939239 | ||||||
| chr9:83939302 | C | T | 10 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(7): Show |
122 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*209G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 209 | chr9 | 83939302 | ||||||
| chr9:83939318 | C | T | 1 | a0001c0001t0017 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*193G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 193 | chr9 | 83939318 | ||||||
| chr9:83939467 | T | C | 1 | a0001c0001t0034 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*44A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 44 | chr9 | 83939467 | ||||||
| chr9:83939474 | C | T | 3 | a0003c0004t0014 a0003c0004t0021 a0003c0005t0014 |
3 | HG02257.hp1 HG02809.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*37G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 4/4 | 37 | chr9 | 83939474 | ||||||
| chr9:83956539 | C | T | 1 | a0001c0001t0010 | 4 | HG01516.hp1 HG01517.hp2 HG02004.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-39G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/4 | 39 | chr9 | 83956539 | ||||||
| chr9:83956545 | C | A | 1 | a0001c0001t0035 | 1 | NA18963.hp1 | 5_prime_UTR_variant | MODIFIER | c.-45G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/4 | 45 | chr9 | 83956545 | ||||||
| chr9:83956553 | G | A | 1 | a0001c0001t0027 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-53C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/4 | 53 | chr9 | 83956553 | ||||||
| chr9:83956589 | G | C | 1 | a0001c0001t0028 | 1 | NA19011.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-89C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/4 | chr9 | 83956589 | |||||||
| chr9:83956653 | A | G | 1 | a0001c0001t0020 | 1 | HG03927.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-153T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/4 | chr9 | 83956653 | |||||||
| chr9:83956696 | A | G | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
209 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(206): Show |
5_prime_UTR_variant | MODIFIER | c.-196T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/4 | 196 | chr9 | 83956696 | ||||||
| chr9:83956721 | G | A | 1 | a0001c0001t0036 | 1 | HG03017.hp1 | 5_prime_UTR_variant | MODIFIER | c.-221C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/4 | 221 | chr9 | 83956721 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:83939764 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.794-21T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83939764 | |||||||
| chr9:83939873 | T | C | 2 | a0001c0001t0002g0089 a0001c0001t0002g0090 |
2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.794-130A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83939873 | |||||||
| chr9:83940225 | C | T | 1 | a0001c0001t0011g0096 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.794-482G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940225 | |||||||
| chr9:83940230 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.794-487G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940230 | |||||||
| chr9:83940369 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.794-626C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940369 | |||||||
| chr9:83940416 | T | A | 1 | a0001c0007t0015g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.794-673A>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940416 | |||||||
| chr9:83940446 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.794-703C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940446 | |||||||
| chr9:83940519 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.794-776G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940519 | |||||||
| chr9:83940530 | G | C | 1 | a0001c0001t0009g0035 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.794-787C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940530 | |||||||
| chr9:83940849 | C | G | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.794-1106G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940849 | |||||||
| chr9:83940900 | G | A | 1 | a0001c0001t0015g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.794-1157C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940900 | |||||||
| chr9:83940958 | A | G | 1 | a0001c0001t0002g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794-1215T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940958 | |||||||
| chr9:83940969 | C | A | 1 | a0001c0001t0009g0112 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.794-1226G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83940969 | |||||||
| chr9:83941068 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.794-1325C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941068 | |||||||
| chr9:83941173 | C | T | 1 | a0001c0001t0015g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.794-1430G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941173 | |||||||
| chr9:83941350 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.794-1607C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941350 | |||||||
| chr9:83941577 | T | G | 1 | a0001c0001t0003g0120 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.794-1834A>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941577 | |||||||
| chr9:83941612 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.794-1869T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941612 | |||||||
| chr9:83941684 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0004g0109 |
2 | HG00423.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.794-1941C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941684 | |||||||
| chr9:83941875 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.794-2132A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941875 | |||||||
| chr9:83941901 | C | T | 1 | a0001c0001t0027g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.794-2158G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941901 | |||||||
| chr9:83941916 | A | G | 61 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(58): Show |
109 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.794-2173T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941916 | |||||||
| chr9:83941938 | G | C | 2 | a0001c0001t0002g0079 a0001c0001t0013g0026 |
3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.794-2195C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83941938 | |||||||
| chr9:83942176 | T | G | 29 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(26): Show |
46 | HG00323.hp1 HG00438.hp1 HG01515.hp2 others(43): Show |
intron_variant | MODIFIER | c.794-2433A>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83942176 | |||||||
| chr9:83942631 | T | C | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.793+2163A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83942631 | |||||||
| chr9:83942835 | T | C | 23 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0013 others(20): Show |
47 | HG00609.hp2 HG00735.hp2 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.793+1959A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83942835 | |||||||
| chr9:83943067 | C | T | 10 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.793+1727G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943067 | |||||||
| chr9:83943169 | G | A | 4 | a0001c0007t0015g0138 a0003c0004t0014g0137 a0003c0004t0021g0136 others(1): Show |
4 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+1625C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943169 | |||||||
| chr9:83943203 | C | T | 9 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0187 others(6): Show |
9 | HG01081.hp1 HG01106.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.793+1591G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943203 | |||||||
| chr9:83943212 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.793+1582G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943212 | |||||||
| chr9:83943217 | G | T | 5 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(2): Show |
6 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+1577C>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943217 | |||||||
| chr9:83943297 | G | A | 10 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(7): Show |
11 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.793+1497C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943297 | |||||||
| chr9:83943331 | C | CA | 27 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(24): Show |
31 | HG00140.hp2 HG00438.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.793+1462dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943331 | |||||||
| chr9:83943331 | C | CAAA | 3 | a0001c0001t0009g0112 a0002c0002t0005g0012 a0002c0002t0005g0111 |
6 | HG02055.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+1460_793+1462d others(5): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943331 | |||||||
| chr9:83943331 | CAAAAAAA others(1): Show |
C | 61 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(58): Show |
109 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.793+1455_793+1462d others(10): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943331 | |||||||
| chr9:83943331 | CAAAAAAA others(7): Show |
C | 8 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(5): Show |
15 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.793+1449_793+1462d others(16): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943331 | |||||||
| chr9:83943331 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0008g0145 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.793+1448_793+1462d others(17): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943331 | |||||||
| chr9:83943331 | CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0002g0017 a0001c0001t0002g0101 a0001c0001t0002g0106 |
5 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+1446_793+1462d others(19): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943331 | |||||||
| chr9:83943355 | A | G | 35 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0016 others(32): Show |
62 | HG00609.hp1 HG00621.hp2 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.793+1439T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943355 | |||||||
| chr9:83943376 | T | C | 1 | a0001c0001t0002g0015 | 3 | HG02109.hp1 HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.793+1418A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943376 | |||||||
| chr9:83943429 | CA | C | 11 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(8): Show |
12 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.793+1364delT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943429 | |||||||
| chr9:83943546 | T | C | 2 | a0001c0001t0002g0067 a0001c0001t0002g0087 |
2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.793+1248A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943546 | |||||||
| chr9:83943568 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.793+1226C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943568 | |||||||
| chr9:83943613 | A | T | 1 | a0001c0001t0023g0064 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.793+1181T>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943613 | |||||||
| chr9:83943817 | C | T | 1 | a0001c0001t0034g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.793+977G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943817 | |||||||
| chr9:83943906 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.793+888T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943906 | |||||||
| chr9:83943913 | C | T | 1 | a0001c0001t0015g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.793+881G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83943913 | |||||||
| chr9:83944016 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.793+778C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944016 | |||||||
| chr9:83944019 | T | TCAAACAA others(5): Show |
5 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(2): Show |
6 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+763_793+774dup others(12): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944019 | |||||||
| chr9:83944019 | T | TCAAACAA others(9): Show |
14 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(11): Show |
21 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.793+774_793+775ins others(16): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944019 | |||||||
| chr9:83944028 | C | CAAACAAA others(13): Show |
9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.793+765_793+766ins others(20): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944028 | |||||||
| chr9:83944059 | C | T | 2 | a0001c0001t0003g0013 a0001c0001t0003g0117 |
5 | HG01257.hp1 HG01258.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+735G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944059 | |||||||
| chr9:83944078 | T | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0050 |
3 | HG02559.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.793+716A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944078 | |||||||
| chr9:83944189 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(68): Show |
122 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.793+605G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944189 | |||||||
| chr9:83944298 | T | C | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(60): Show |
111 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.793+496A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944298 | |||||||
| chr9:83944347 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0101 a0001c0001t0002g0106 |
5 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+447C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944347 | |||||||
| chr9:83944375 | T | A | 1 | a0001c0001t0023g0064 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.793+419A>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944375 | |||||||
| chr9:83944384 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.793+410A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944384 | |||||||
| chr9:83944444 | A | G | 5 | a0001c0001t0015g0135 a0001c0007t0015g0138 a0003c0004t0014g0137 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+350T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944444 | |||||||
| chr9:83944604 | C | G | 1 | a0004c0003t0005g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.793+190G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944604 | |||||||
| chr9:83944744 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.793+50G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944744 | |||||||
| chr9:83944758 | T | G | 1 | a0001c0001t0002g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.793+36A>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 3/3 | chr9 | 83944758 | |||||||
| chr9:83945095 | T | C | 5 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(2): Show |
6 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-106A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945095 | |||||||
| chr9:83945253 | T | A | 1 | a0001c0001t0002g0068 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.598-264A>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945253 | |||||||
| chr9:83945263 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.598-274C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945263 | |||||||
| chr9:83945400 | C | CA | 9 | a0001c0001t0001g0193 a0001c0001t0002g0022 a0001c0001t0002g0024 others(6): Show |
11 | HG01255.hp1 HG02683.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-412dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945400 | |||||||
| chr9:83945400 | CA | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0021 others(60): Show |
111 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.598-412delT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945400 | |||||||
| chr9:83945400 | CAA | C | 15 | a0001c0001t0003g0133 a0001c0001t0007g0030 a0001c0001t0007g0092 others(12): Show |
22 | HG01517.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.598-413_598-412del others(2): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945400 | |||||||
| chr9:83945616 | T | A | 1 | a0001c0001t0003g0121 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.598-627A>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945616 | |||||||
| chr9:83945625 | G | A | 1 | a0001c0001t0026g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.598-636C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945625 | |||||||
| chr9:83945747 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.598-758C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945747 | |||||||
| chr9:83945757 | CGCCCG | C | 3 | a0001c0001t0002g0017 a0001c0001t0002g0101 a0001c0001t0002g0106 |
5 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-773_598-769del others(5): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945757 | |||||||
| chr9:83945853 | C | T | 1 | a0001c0001t0002g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.598-864G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83945853 | |||||||
| chr9:83946044 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.598-1055G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946044 | |||||||
| chr9:83946089 | G | A | 1 | a0001c0001t0004g0108 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.598-1100C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946089 | |||||||
| chr9:83946259 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.598-1270G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946259 | |||||||
| chr9:83946330 | C | A | 2 | a0002c0002t0005g0012 a0002c0002t0005g0111 |
5 | HG02055.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-1341G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946330 | |||||||
| chr9:83946435 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.598-1446T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946435 | |||||||
| chr9:83946479 | A | G | 9 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(6): Show |
16 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-1490T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946479 | |||||||
| chr9:83946842 | G | A | 5 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(2): Show |
6 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-1853C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946842 | |||||||
| chr9:83946904 | A | AT | 5 | a0001c0001t0001g0020 a0001c0001t0001g0224 a0001c0001t0002g0089 others(2): Show |
7 | HG00735.hp2 HG02080.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-1916dupA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946904 | |||||||
| chr9:83946919 | T | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0101 a0001c0001t0002g0106 |
5 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-1930A>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946919 | |||||||
| chr9:83946942 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0050 |
3 | HG02559.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.598-1953C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946942 | |||||||
| chr9:83946953 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG02015.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.598-1964G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83946953 | |||||||
| chr9:83947031 | A | C | 2 | a0001c0001t0008g0167 a0001c0001t0008g0219 |
2 | HG01255.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.598-2042T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947031 | |||||||
| chr9:83947034 | A | G | 5 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(2): Show |
10 | HG02055.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.598-2045T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947034 | |||||||
| chr9:83947127 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.598-2138C>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947127 | |||||||
| chr9:83947243 | C | T | 1 | a0001c0001t0004g0108 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.598-2254G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947243 | |||||||
| chr9:83947772 | C | T | 5 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0171 others(2): Show |
5 | HG00438.hp1 NA18950.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-2783G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947772 | |||||||
| chr9:83947774 | C | T | 22 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0025 others(19): Show |
43 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.598-2785G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947774 | |||||||
| chr9:83947897 | T | C | 19 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(16): Show |
25 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.598-2908A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947897 | |||||||
| chr9:83947937 | C | G | 1 | a0001c0001t0015g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.598-2948G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947937 | |||||||
| chr9:83947938 | G | A | 1 | a0001c0001t0018g0194 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.598-2949C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947938 | |||||||
| chr9:83947965 | TGGCCGCC others(32): Show |
T | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.598-3015_598-2977d others(41): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83947965 | |||||||
| chr9:83948041 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.598-3052G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948041 | |||||||
| chr9:83948042 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.598-3053C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948042 | |||||||
| chr9:83948205 | A | AC | 13 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0180 others(10): Show |
15 | HG00423.hp1 HG00621.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.598-3217dupG | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948205 | |||||||
| chr9:83948210 | G | C | 1 | a0001c0001t0002g0063 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.598-3221C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948210 | |||||||
| chr9:83948230 | T | C | 28 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(25): Show |
41 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(38): Show |
intron_variant | MODIFIER | c.598-3241A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948230 | |||||||
| chr9:83948237 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598-3248G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948237 | |||||||
| chr9:83948241 | C | T | 1 | a0001c0001t0026g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.598-3252G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948241 | |||||||
| chr9:83948275 | AGCAGCCG others(33): Show |
A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(6): Show |
16 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-3326_598-3287d others(42): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948275 | |||||||
| chr9:83948281 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA20805.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.598-3292G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948281 | |||||||
| chr9:83948306 | CCTCCGCC others(33): Show |
C | 24 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0013 others(21): Show |
48 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.598-3357_598-3318d others(42): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948306 | |||||||
| chr9:83948309 | C | T | 1 | a0001c0001t0036g0230 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.598-3320G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948309 | |||||||
| chr9:83948322 | G | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(6): Show |
16 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-3333C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948322 | |||||||
| chr9:83948402 | G | A | 4 | a0001c0007t0015g0138 a0003c0004t0014g0137 a0003c0004t0021g0136 others(1): Show |
4 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-3413C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948402 | |||||||
| chr9:83948410 | C | A | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.598-3421G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948410 | |||||||
| chr9:83948416 | CGGGAGGG others(41): Show |
C | 14 | a0001c0001t0002g0010 a0001c0001t0002g0051 a0001c0001t0002g0053 others(11): Show |
19 | HG01106.hp1 HG01123.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.598-3475_598-3428d others(50): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948416 | |||||||
| chr9:83948443 | C | G | 1 | a0001c0001t0002g0003 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.598-3454G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948443 | |||||||
| chr9:83948448 | G | A | 1 | a0001c0001t0033g0189 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.598-3459C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948448 | |||||||
| chr9:83948500 | G | A | 1 | a0001c0001t0007g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.598-3511C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948500 | |||||||
| chr9:83948509 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.598-3520C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948509 | |||||||
| chr9:83948512 | A | AG | 53 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0019 others(50): Show |
73 | HG00323.hp1 HG00438.hp1 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.598-3524dupC | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948512 | |||||||
| chr9:83948515 | G | T | 28 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(25): Show |
41 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(38): Show |
intron_variant | MODIFIER | c.598-3526C>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948515 | |||||||
| chr9:83948540 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.598-3551G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948540 | |||||||
| chr9:83948577 | A | AC | 4 | a0001c0001t0003g0114 a0001c0001t0004g0109 a0001c0001t0007g0092 others(1): Show |
4 | HG00423.hp2 HG02055.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-3589dupG | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948577 | |||||||
| chr9:83948580 | A | C | 123 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(120): Show |
211 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.598-3591T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948580 | |||||||
| chr9:83948628 | C | T | 25 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0013 others(22): Show |
49 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.598-3639G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948628 | |||||||
| chr9:83948647 | T | C | 9 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(6): Show |
16 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.598-3658A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948647 | |||||||
| chr9:83948649 | GA | G | 3 | a0003c0004t0014g0137 a0003c0004t0021g0136 a0003c0005t0014g0049 |
3 | HG02257.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.598-3661delT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948649 | |||||||
| chr9:83948676 | A | C | 2 | a0001c0001t0002g0059 a0001c0001t0002g0074 |
2 | HG00738.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.598-3687T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948676 | |||||||
| chr9:83948803 | G | C | 3 | a0003c0004t0014g0137 a0003c0004t0021g0136 a0003c0005t0014g0049 |
3 | HG02257.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.598-3814C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948803 | |||||||
| chr9:83948810 | C | T | 3 | a0001c0001t0003g0123 a0001c0001t0003g0125 a0001c0001t0003g0127 |
3 | NA19060.hp2 NA19072.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.598-3821G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948810 | |||||||
| chr9:83948834 | A | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(26): Show |
46 | HG00323.hp1 HG00438.hp1 HG01515.hp2 others(43): Show |
intron_variant | MODIFIER | c.598-3845T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948834 | |||||||
| chr9:83948848 | A | T | 28 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(25): Show |
41 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(38): Show |
intron_variant | MODIFIER | c.598-3859T>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948848 | |||||||
| chr9:83948955 | C | T | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.598-3966G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83948955 | |||||||
| chr9:83949037 | T | TC | 99 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(96): Show |
163 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.598-4049dupG | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949037 | |||||||
| chr9:83949039 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.598-4050C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949039 | |||||||
| chr9:83949039 | G | T | 99 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(96): Show |
163 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.598-4050C>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949039 | |||||||
| chr9:83949095 | T | TA | 7 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0004g0108 others(4): Show |
7 | HG02257.hp1 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-4107dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949095 | |||||||
| chr9:83949095 | TA | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0144 a0001c0001t0001g0157 others(6): Show |
10 | HG01943.hp1 HG01975.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-4107delT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949095 | |||||||
| chr9:83949416 | G | A | 1 | a0001c0001t0012g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.598-4427C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949416 | |||||||
| chr9:83949481 | T | TA | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.598-4493dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949481 | |||||||
| chr9:83949578 | C | G | 155 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(152): Show |
261 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.598-4589G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949578 | |||||||
| chr9:83949618 | C | T | 2 | a0001c0001t0010g0018 a0001c0001t0010g0142 |
4 | HG01516.hp1 HG01517.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-4629G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949618 | |||||||
| chr9:83949667 | C | CA | 8 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0225 others(5): Show |
10 | HG01106.hp1 HG02559.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.598-4679dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949667 | |||||||
| chr9:83949671 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.598-4682T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949671 | |||||||
| chr9:83949673 | A | C | 3 | a0003c0004t0014g0137 a0003c0004t0021g0136 a0003c0005t0014g0049 |
3 | HG02257.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.598-4684T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949673 | |||||||
| chr9:83949988 | A | G | 19 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(16): Show |
25 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.598-4999T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83949988 | |||||||
| chr9:83950049 | A | AT | 9 | a0001c0001t0001g0177 a0001c0001t0001g0200 a0001c0001t0001g0217 others(6): Show |
9 | HG02055.hp1 HG02738.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-5061dupA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950049 | |||||||
| chr9:83950049 | AT | A | 26 | a0001c0001t0001g0198 a0001c0001t0002g0080 a0001c0001t0002g0082 others(23): Show |
50 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.598-5061delA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950049 | |||||||
| chr9:83950175 | G | C | 5 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(2): Show |
6 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-5186C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950175 | |||||||
| chr9:83950203 | A | C | 19 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(16): Show |
25 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.597+5178T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950203 | |||||||
| chr9:83950294 | T | C | 19 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(16): Show |
25 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.597+5087A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950294 | |||||||
| chr9:83950310 | A | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(26): Show |
46 | HG00323.hp1 HG00438.hp1 HG01515.hp2 others(43): Show |
intron_variant | MODIFIER | c.597+5071T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950310 | |||||||
| chr9:83950315 | A | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(26): Show |
46 | HG00323.hp1 HG00438.hp1 HG01515.hp2 others(43): Show |
intron_variant | MODIFIER | c.597+5066T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950315 | |||||||
| chr9:83950332 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.597+5049C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950332 | |||||||
| chr9:83950340 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.597+5041C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950340 | |||||||
| chr9:83950390 | G | C | 20 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0025 others(17): Show |
40 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.597+4991C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950390 | |||||||
| chr9:83950395 | C | A | 1 | a0001c0001t0002g0081 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.597+4986G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950395 | |||||||
| chr9:83950407 | G | C | 1 | a0001c0001t0002g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.597+4974C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950407 | |||||||
| chr9:83950596 | CT | C | 135 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(132): Show |
226 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.597+4784delA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950596 | |||||||
| chr9:83950596 | CTT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0169 a0001c0001t0003g0124 others(8): Show |
18 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.597+4783_597+4784d others(4): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950596 | |||||||
| chr9:83950596 | CTTT | C | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+4782_597+4784d others(5): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950596 | |||||||
| chr9:83950648 | C | G | 1 | a0001c0007t0015g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.597+4733G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950648 | |||||||
| chr9:83950883 | G | C | 2 | a0001c0001t0002g0027 a0001c0001t0002g0086 |
3 | HG01192.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.597+4498C>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83950883 | |||||||
| chr9:83951140 | G | A | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+4241C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83951140 | |||||||
| chr9:83951542 | CAGCGAGA others(10): Show |
C | 1 | a0001c0001t0001g0151 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.597+3822_597+3838d others(19): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83951542 | |||||||
| chr9:83951546 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(26): Show |
46 | HG00323.hp1 HG00438.hp1 HG01515.hp2 others(43): Show |
intron_variant | MODIFIER | c.597+3835C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83951546 | |||||||
| chr9:83951735 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.597+3646G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83951735 | |||||||
| chr9:83951765 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.597+3616G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83951765 | |||||||
| chr9:83951988 | T | C | 1 | a0001c0001t0002g0082 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.597+3393A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83951988 | |||||||
| chr9:83952081 | G | T | 1 | a0001c0001t0003g0124 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.597+3300C>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952081 | |||||||
| chr9:83952140 | A | G | 1 | a0001c0001t0030g0156 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.597+3241T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952140 | |||||||
| chr9:83952241 | C | T | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+3140G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952241 | |||||||
| chr9:83952279 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.597+3102A>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952279 | |||||||
| chr9:83952323 | A | C | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+3058T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952323 | |||||||
| chr9:83952346 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.597+3035A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952346 | |||||||
| chr9:83952523 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0199 |
2 | HG00642.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.597+2858G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952523 | |||||||
| chr9:83952635 | A | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0101 a0001c0001t0002g0106 |
5 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+2746T>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952635 | |||||||
| chr9:83952664 | G | A | 1 | a0001c0001t0017g0039 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.597+2717C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952664 | |||||||
| chr9:83952751 | C | T | 5 | a0001c0001t0007g0030 a0001c0001t0007g0092 a0001c0001t0007g0093 others(2): Show |
6 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.597+2630G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952751 | |||||||
| chr9:83952794 | G | GA | 43 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0046 others(40): Show |
55 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.597+2586dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952794 | |||||||
| chr9:83952803 | A | C | 2 | a0004c0003t0005g0132 a0004c0003t0025g0130 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.597+2578T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952803 | |||||||
| chr9:83952805 | A | C | 2 | a0001c0001t0001g0209 a0001c0001t0036g0230 |
2 | HG00423.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.597+2576T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952805 | |||||||
| chr9:83952808 | A | C | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+2573T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952808 | |||||||
| chr9:83952813 | C | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(26): Show |
46 | HG00438.hp1 HG01515.hp2 HG01516.hp1 others(43): Show |
intron_variant | MODIFIER | c.597+2568G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952813 | |||||||
| chr9:83952865 | G | T | 5 | a0001c0001t0015g0135 a0001c0007t0015g0138 a0003c0004t0014g0137 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+2516C>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952865 | |||||||
| chr9:83952892 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0050 |
3 | HG02559.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.597+2489C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952892 | |||||||
| chr9:83952923 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.597+2458C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952923 | |||||||
| chr9:83952959 | C | CA | 15 | a0001c0001t0001g0047 a0001c0001t0001g0171 a0001c0001t0001g0172 others(12): Show |
16 | HG00140.hp2 HG00423.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.597+2421dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83952959 | |||||||
| chr9:83953073 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.597+2308T>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953073 | |||||||
| chr9:83953326 | C | A | 2 | a0001c0001t0002g0089 a0001c0001t0002g0090 |
2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.597+2055G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953326 | |||||||
| chr9:83953328 | C | G | 156 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0019 others(153): Show |
262 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.597+2053G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953328 | |||||||
| chr9:83953346 | C | CT | 10 | a0001c0001t0001g0155 a0001c0001t0001g0218 a0001c0001t0002g0058 others(7): Show |
10 | HG00609.hp1 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.597+2034dupA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953346 | |||||||
| chr9:83953346 | CT | C | 7 | a0001c0001t0001g0212 a0001c0001t0001g0228 a0001c0001t0002g0089 others(4): Show |
13 | HG00423.hp2 HG02040.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.597+2034delA | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953346 | |||||||
| chr9:83953449 | G | A | 1 | a0001c0007t0015g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.597+1932C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953449 | |||||||
| chr9:83953491 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.597+1890C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953491 | |||||||
| chr9:83953776 | T | G | 1 | a0001c0001t0001g0214 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.597+1605A>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953776 | |||||||
| chr9:83953779 | C | A | 1 | a0001c0001t0001g0214 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.597+1602G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953779 | |||||||
| chr9:83953782 | A | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0050 |
3 | HG02559.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.597+1599T>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953782 | |||||||
| chr9:83953880 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0091 |
3 | HG01192.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.597+1501C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953880 | |||||||
| chr9:83953934 | G | A | 1 | a0004c0003t0005g0131 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.597+1447C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953934 | |||||||
| chr9:83953959 | A | G | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(68): Show |
122 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.597+1422T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83953959 | |||||||
| chr9:83954261 | G | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0033 a0001c0001t0004g0104 others(6): Show |
16 | HG00423.hp2 HG00438.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.597+1120C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954261 | |||||||
| chr9:83954266 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.597+1115T>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954266 | |||||||
| chr9:83954289 | AAGG | A | 5 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0011g0096 others(2): Show |
5 | HG02258.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+1089_597+1091d others(5): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954289 | |||||||
| chr9:83954299 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.597+1082A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954299 | |||||||
| chr9:83954554 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.597+827G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954554 | |||||||
| chr9:83954604 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.597+777G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954604 | |||||||
| chr9:83954621 | C | T | 1 | a0001c0001t0006g0055 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.597+760G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954621 | |||||||
| chr9:83954788 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.597+593C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954788 | |||||||
| chr9:83954849 | T | C | 4 | a0001c0007t0015g0138 a0003c0004t0014g0137 a0003c0004t0021g0136 others(1): Show |
4 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+532A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954849 | |||||||
| chr9:83954879 | C | CA | 20 | a0001c0001t0001g0009 a0001c0001t0001g0217 a0001c0001t0001g0218 others(17): Show |
30 | HG01106.hp2 HG01255.hp1 HG02135.hp1 others(27): Show |
intron_variant | MODIFIER | c.597+501dupT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954879 | |||||||
| chr9:83954879 | CA | C | 19 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
29 | HG00621.hp2 HG01256.hp1 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.597+501delT | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954879 | |||||||
| chr9:83954879 | CAA | C | 65 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(62): Show |
113 | HG00099.hp1 HG00140.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.597+500_597+501del others(2): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954879 | |||||||
| chr9:83954879 | CAAA | C | 7 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(4): Show |
7 | HG01167.hp1 HG01167.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.597+499_597+501del others(3): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954879 | |||||||
| chr9:83954879 | CAAAAAAA | C | 7 | a0001c0001t0009g0034 a0001c0001t0009g0112 a0001c0001t0026g0110 others(4): Show |
11 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.597+495_597+501del others(7): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954879 | |||||||
| chr9:83954879 | CAAAAAAA others(8): Show |
C | 1 | a0003c0004t0021g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.597+487_597+501del others(15): Show |
QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83954879 | |||||||
| chr9:83955136 | T | C | 9 | a0001c0001t0009g0034 a0001c0001t0009g0035 a0001c0001t0009g0112 others(6): Show |
14 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+245A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83955136 | |||||||
| chr9:83955160 | C | T | 99 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(96): Show |
163 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.597+221G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83955160 | |||||||
| chr9:83955175 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.597+206G>A | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83955175 | |||||||
| chr9:83955232 | A | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0050 |
3 | HG02559.hp1 HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.597+149T>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 2/3 | chr9 | 83955232 | |||||||
| chr9:83955699 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.338-59G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/3 | chr9 | 83955699 | |||||||
| chr9:83955746 | G | A | 2 | a0001c0001t0003g0133 a0001c0001t0003g0134 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.338-106C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/3 | chr9 | 83955746 | |||||||
| chr9:83955796 | C | G | 1 | a0001c0001t0015g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.338-156G>C | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/3 | chr9 | 83955796 | |||||||
| chr9:83955918 | T | C | 1 | a0001c0001t0015g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.337+246A>G | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/3 | chr9 | 83955918 | |||||||
| chr9:83956000 | C | A | 4 | a0001c0007t0015g0138 a0003c0004t0014g0137 a0003c0004t0021g0136 others(1): Show |
4 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+164G>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/3 | chr9 | 83956000 | |||||||
| chr9:83956030 | G | A | 1 | a0001c0001t0006g0139 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.337+134C>T | QNG1 | ENSG00000165118.15 | transcript | ENST00000376344.8 | protein_coding | 1/3 | chr9 | 83956030 |