Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91543 |
| ensemblid | ENSG00000134321.13 |
| hgncid | 30908 |
| symbol | RSAD2 |
| name | radical S-adenosyl methionine domain containing 2 |
| refseq_nuc | NM_080657.5 |
| refseq_prot | NP_542388.2 |
| ensembl_nuc | ENST00000382040.4 |
| ensembl_prot | ENSP00000371471.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 6877777 |
| end | 6898239 |
| strand | + |
| ver | v1.2 |
| region | chr2:6877777-6898239 |
| region5000 | chr2:6872777-6903239 |
| regionname0 | RSAD2_chr2_6877777_6898239 |
| regionname5000 | RSAD2_chr2_6872777_6903239 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 361 | 336 | 92 | 62 | 118 | 16 | 46 | 82 | RSAD2_chr2_6872777_6903239 | RSAD2 | MWVLT others(356): Show |
chr2 | 6872777 | 6903239 |
| a0002 | 0/0 | 361 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | MWVLT others(356): Show |
chr2 | 6872777 | 6903239 |
| a0003 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | MWVLT others(356): Show |
chr2 | 6872777 | 6903239 |
| a0004 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | MWVLT others(356): Show |
chr2 | 6872777 | 6903239 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1083 | 322 | 82 | 61 | 115 | 16 | 46 | RSAD2_chr2_6872777_6903239 | RSAD2 | ATGTG others(1078): Show |
chr2 | 6872777 | 6903239 | ||
| a0001c0002 | 0/0 | 1083 | 5 | 5 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | ATGTG others(1078): Show |
chr2 | 6872777 | 6903239 | ||
| a0001c0003 | 0/0 | 1083 | 4 | 0 | 1 | 3 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | ATGTG others(1078): Show |
chr2 | 6872777 | 6903239 | ||
| a0001c0004 | 0/0 | 1083 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | ATGTG others(1078): Show |
chr2 | 6872777 | 6903239 | ||
| a0001c0007 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | ATGTG others(1078): Show |
chr2 | 6872777 | 6903239 | ||
| a0001c0008 | 0/0 | 1083 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | ATGTG others(1078): Show |
chr2 | 6872777 | 6903239 | ||
| a0002c0005 | 0/0 | 1083 | 2 | 2 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | ATGTG others(1078): Show |
chr2 | 6872777 | 6903239 | ||
| a0003c0009 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | ATGTG others(1078): Show |
chr2 | 6872777 | 6903239 | ||
| a0004c0006 | 0/0 | 1083 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | ATGTG others(1078): Show |
chr2 | 6872777 | 6903239 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3409 | 138 | 24 | 30 | 59 | 5 | 20 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0002 | 1/0 | 3407 | 47 | 11 | 8 | 22 | 1 | 4 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3402): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0003 | 0/0 | 3408 | 25 | 0 | 7 | 13 | 3 | 2 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0004 | 0/0 | 3408 | 13 | 0 | 1 | 5 | 2 | 5 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0005 | 0/1 | 3408 | 12 | 4 | 5 | 0 | 1 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0006 | 0/0 | 3410 | 12 | 5 | 1 | 0 | 1 | 5 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3405): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0007 | 0/0 | 3408 | 10 | 10 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0008 | 0/0 | 3410 | 5 | 4 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3405): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0009 | 0/0 | 3417 | 6 | 6 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3412): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0010 | 0/0 | 3411 | 6 | 0 | 0 | 6 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3406): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0011 | 0/0 | 3409 | 5 | 0 | 3 | 2 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0012 | 0/0 | 3408 | 4 | 0 | 1 | 2 | 1 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0013 | 0/0 | 3410 | 4 | 4 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3405): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0014 | 0/0 | 3409 | 4 | 0 | 0 | 0 | 1 | 3 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0016 | 0/0 | 3409 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0017 | 0/0 | 3409 | 2 | 2 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0018 | 0/0 | 3407 | 2 | 0 | 1 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3402): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0019 | 0/0 | 3408 | 2 | 2 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0020 | 0/0 | 3408 | 2 | 0 | 0 | 2 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0021 | 0/0 | 3411 | 2 | 1 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3406): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0022 | 0/0 | 3409 | 2 | 0 | 1 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0023 | 0/0 | 3410 | 2 | 0 | 0 | 2 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3405): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0024 | 0/0 | 3409 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0026 | 0/0 | 3409 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0027 | 0/0 | 3408 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0028 | 0/0 | 3407 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3402): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0029 | 0/0 | 3408 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0030 | 0/0 | 3409 | 1 | 0 | 0 | 0 | 1 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0031 | 0/0 | 3417 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3412): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0032 | 0/0 | 3409 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0033 | 0/0 | 3410 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3405): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0034 | 0/0 | 3411 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3406): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0036 | 0/0 | 3409 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0037 | 0/0 | 3411 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3406): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0039 | 0/0 | 3409 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0001t0040 | 0/0 | 3408 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0001c0002t0008 | 0/0 | 3410 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3405): Show |
chr2 | 6872777 | 6903239 |
| a0001c0002t0017 | 0/0 | 3409 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0002t0035 | 0/0 | 3409 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0003t0001 | 0/0 | 3409 | 4 | 0 | 1 | 3 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0001c0004t0015 | 0/0 | 3410 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3405): Show |
chr2 | 6872777 | 6903239 |
| a0001c0007t0038 | 0/0 | 3410 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3405): Show |
chr2 | 6872777 | 6903239 |
| a0001c0008t0025 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3402): Show |
chr2 | 6872777 | 6903239 |
| a0002c0005t0003 | 0/0 | 3408 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| a0002c0005t0015 | 0/0 | 3410 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3405): Show |
chr2 | 6872777 | 6903239 |
| a0003c0009t0001 | 0/0 | 3409 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3404): Show |
chr2 | 6872777 | 6903239 |
| a0004c0006t0004 | 0/0 | 3408 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | GCTCT others(3403): Show |
chr2 | 6872777 | 6903239 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 68 | 11 | 12 | 33 | 4 | 8 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0013 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0002 | 0/0 | 24 | 0 | 5 | 15 | 0 | 4 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0003g0003 | 0/0 | 19 | 0 | 5 | 11 | 1 | 2 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0004g0004 | 0/0 | 7 | 0 | 1 | 0 | 2 | 4 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0004g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0005g0006 | 0/1 | 7 | 1 | 3 | 0 | 1 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0005g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0006g0009 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0006g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0007g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0007g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0008g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0009g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0010g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0011g0011 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0012g0010 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0012g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0012g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0013g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0013g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0014g0005 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0016g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0017g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0017g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0018g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0019g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0020g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0021g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0021g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0022g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0023g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0023g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0024g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0026g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0027g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0028g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0029g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0030g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0031g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0032g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0033g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0034g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0036g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0037g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0039g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0001t0040g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0002t0008g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0002t0017g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0002t0035g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0004t0015g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0007t0038g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0001c0008t0025g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0002c0005t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0002c0005t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0003c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| a0004c0006t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0097 | EUR | GBR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00140 | hp2 | a0001 | c0001 | t0014 | g0005 | EUR | GBR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0028 | EUR | FIN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0006 | EUR | FIN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00408 | hp1 | a0001 | c0001 | t0023 | g0001 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00408 | hp2 | a0001 | c0001 | t0023 | g0022 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00741 | hp1 | a0001 | c0001 | t0011 | g0011 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0014 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01099 | hp2 | a0001 | c0001 | t0012 | g0028 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01109 | hp1 | a0001 | c0001 | t0028 | g0023 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01168 | hp1 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0036 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01261 | hp1 | a0001 | c0001 | t0032 | g0083 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0004 | EUR | IBS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0034 | EUR | IBS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0034 | EUR | IBS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | IBS | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0109 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0036 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01943 | hp1 | a0001 | c0001 | t0022 | g0001 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01943 | hp2 | a0001 | c0001 | t0011 | g0011 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02055 | hp2 | a0001 | c0001 | t0016 | g0001 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02080 | hp1 | a0003 | c0009 | t0001 | g0001 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02145 | hp2 | a0001 | c0007 | t0038 | g0078 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02155 | hp1 | a0001 | c0001 | t0011 | g0011 | EAS | CDX | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0050 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02273 | hp2 | a0001 | c0001 | t0011 | g0011 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0116 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02451 | hp1 | a0001 | c0001 | t0034 | g0080 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02451 | hp2 | a0001 | c0004 | t0015 | g0019 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02523 | hp1 | a0004 | c0006 | t0004 | g0008 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02602 | hp2 | a0001 | c0001 | t0014 | g0005 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02615 | hp2 | a0001 | c0001 | t0031 | g0046 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02647 | hp1 | a0001 | c0001 | t0037 | g0001 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0043 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0009 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02717 | hp1 | a0001 | c0001 | t0016 | g0001 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02723 | hp1 | a0001 | c0002 | t0008 | g0016 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0009 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02886 | hp1 | a0002 | c0005 | t0003 | g0056 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02922 | hp2 | a0001 | c0001 | t0013 | g0035 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0035 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02970 | hp2 | a0001 | c0001 | t0024 | g0018 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03130 | hp1 | a0001 | c0002 | t0035 | g0055 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03139 | hp1 | a0001 | c0002 | t0008 | g0016 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03139 | hp2 | a0001 | c0004 | t0015 | g0019 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03225 | hp1 | a0001 | c0001 | t0017 | g0054 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03239 | hp2 | a0001 | c0001 | t0018 | g0004 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0001 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0057 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03486 | hp2 | a0002 | c0005 | t0015 | g0059 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0027 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03579 | hp2 | a0001 | c0002 | t0008 | g0016 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0009 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03654 | hp2 | a0001 | c0001 | t0014 | g0005 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03669 | hp1 | a0001 | c0001 | t0027 | g0068 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0009 | SAS | PJL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03831 | hp2 | a0001 | c0001 | t0033 | g0001 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03927 | hp1 | a0001 | c0001 | t0021 | g0009 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04115 | hp1 | a0001 | c0001 | t0014 | g0005 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0081 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04184 | hp1 | a0001 | c0001 | t0026 | g0004 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04199 | hp1 | a0001 | c0001 | t0036 | g0102 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18522 | hp1 | a0001 | c0004 | t0015 | g0019 | AFR | YRI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | YRI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | YRI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18906 | hp2 | a0001 | c0001 | t0019 | g0027 | AFR | YRI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18942 | hp1 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18942 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18944 | hp2 | a0001 | c0001 | t0022 | g0094 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0106 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18965 | hp1 | a0001 | c0001 | t0012 | g0105 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18968 | hp2 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18973 | hp1 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18994 | hp1 | a0001 | c0001 | t0029 | g0002 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19003 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19009 | hp2 | a0001 | c0001 | t0011 | g0011 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19010 | hp2 | a0001 | c0001 | t0010 | g0073 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | LWK | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | LWK | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19083 | hp2 | a0001 | c0001 | t0012 | g0010 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19088 | hp1 | a0001 | c0001 | t0010 | g0010 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20129 | hp1 | a0001 | c0001 | t0040 | g0053 | AFR | ASW | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0058 | AFR | ASW | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20752 | hp2 | a0001 | c0001 | t0012 | g0010 | EUR | TSI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20805 | hp2 | a0001 | c0001 | t0030 | g0003 | EUR | TSI | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | GIH | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02109 | hp1 | a0001 | c0001 | t0021 | g0040 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02486 | hp1 | a0001 | c0001 | t0039 | g0015 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03471 | hp1 | a0001 | c0008 | t0025 | g0042 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | MSL | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | USA | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | USA | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA20300 | hp2 | a0001 | c0002 | t0017 | g0016 | AFR | USA | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0006 | REF | REF | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0051 | REF | REF | RSAD2_chr2_6872777_6903239 | RSAD2 | chr2 | 6872777 | 6903239 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:6877925 | T | G | 1 | a0002 | 2 | HG02886.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.125T>G | p.Leu42Arg | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/6 | 149/3407 | 125/1086 | 42/361 | chr2 | 6877925 | |||
| chr2:6883418 | C | T | 1 | a0003 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.394C>T | p.Arg132Trp | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/6 | 418/3407 | 394/1086 | 132/361 | chr2 | 6883418 | |||
| chr2:6895781 | C | T | 1 | a0004 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.925C>T | p.Arg309Cys | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 949/3407 | 925/1086 | 309/361 | chr2 | 6895781 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:6877812 | T | C | 1 | a0001c0002 | 5 | HG02723.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.12T>C | p.Leu4Leu | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/6 | 36/3407 | 12/1086 | 4/361 | chr2 | 6877812 | |||
| chr2:6877890 | G | A | 1 | a0001c0003 | 4 | HG02293.hp2 NA18989.hp1 NA19003.hp1 others(1): Show |
synonymous_variant | LOW | c.90G>A | p.Pro30Pro | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/6 | 114/3407 | 90/1086 | 30/361 | chr2 | 6877890 | |||
| chr2:6883444 | G | A | 1 | a0001c0004 | 3 | HG02451.hp2 HG03139.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.420G>A | p.Val140Val | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/6 | 444/3407 | 420/1086 | 140/361 | chr2 | 6883444 | |||
| chr2:6886978 | C | T | 1 | a0001c0008 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.552C>T | p.Asp184Asp | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/6 | 576/3407 | 552/1086 | 184/361 | chr2 | 6886978 | |||
| chr2:6890319 | C | T | 1 | a0001c0007 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.882C>T | p.Asn294Asn | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/6 | 906/3407 | 882/1086 | 294/361 | chr2 | 6890319 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:6896264 | C | G | 1 | a0001c0001t0040 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322C>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 322 | chr2 | 6896264 | ||||||
| chr2:6896272 | A | G | 4 | a0001c0001t0007 a0001c0001t0039 a0001c0001t0040 others(1): Show |
13 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*330A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 330 | chr2 | 6896272 | ||||||
| chr2:6896341 | A | T | 28 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(25): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*399A>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 399 | chr2 | 6896341 | ||||||
| chr2:6896398 | T | C | 9 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0018 others(6): Show |
33 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*456T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 456 | chr2 | 6896398 | ||||||
| chr2:6896490 | A | G | 9 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0018 others(6): Show |
33 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*548A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 548 | chr2 | 6896490 | ||||||
| chr2:6896532 | C | CT | 11 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(8): Show |
49 | HG00280.hp1 HG01099.hp2 HG01884.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*602dupT | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 603 | INFO_REALIGN_3_PRIME | chr2 | 6896532 | |||||
| chr2:6896532 | C | CTT | 15 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(12): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*601_*602dupTT | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 603 | INFO_REALIGN_3_PRIME | chr2 | 6896532 | |||||
| chr2:6896532 | C | CTTT | 6 | a0001c0001t0008 a0001c0001t0023 a0001c0001t0037 others(3): Show |
15 | HG00408.hp1 HG00408.hp2 HG01070.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*600_*602dupTTT | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 603 | INFO_REALIGN_3_PRIME | chr2 | 6896532 | |||||
| chr2:6896547 | C | T | 28 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(25): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*605C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 605 | chr2 | 6896547 | ||||||
| chr2:6896556 | A | G | 1 | a0001c0001t0022 | 2 | HG01943.hp1 NA18944.hp2 |
3_prime_UTR_variant | MODIFIER | c.*614A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 614 | chr2 | 6896556 | ||||||
| chr2:6896616 | C | T | 1 | a0001c0001t0031 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*674C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 674 | chr2 | 6896616 | ||||||
| chr2:6896625 | T | C | 9 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0018 others(6): Show |
33 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*683T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 683 | chr2 | 6896625 | ||||||
| chr2:6896680 | C | T | 21 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(18): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*738C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 738 | chr2 | 6896680 | ||||||
| chr2:6896702 | C | T | 1 | a0001c0001t0036 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*760C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 760 | chr2 | 6896702 | ||||||
| chr2:6896707 | G | C | 13 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(10): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*765G>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 765 | chr2 | 6896707 | ||||||
| chr2:6896735 | T | C | 1 | a0001c0001t0032 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 793 | chr2 | 6896735 | ||||||
| chr2:6896898 | T | C | 4 | a0001c0001t0008 a0001c0001t0017 a0001c0002t0008 others(1): Show |
11 | HG01070.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*956T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 956 | chr2 | 6896898 | ||||||
| chr2:6896936 | G | T | 27 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(24): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*994G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 994 | chr2 | 6896936 | ||||||
| chr2:6896937 | C | T | 27 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(24): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*995C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 995 | chr2 | 6896937 | ||||||
| chr2:6897043 | A | T | 27 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(24): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*1101A>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 1101 | chr2 | 6897043 | ||||||
| chr2:6897054 | C | T | 2 | a0001c0001t0014 a0001c0001t0033 |
5 | HG00140.hp2 HG02602.hp2 HG03654.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1112C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 1112 | chr2 | 6897054 | ||||||
| chr2:6897140 | A | C | 5 | a0001c0001t0004 a0001c0001t0018 a0001c0001t0026 others(2): Show |
18 | HG01168.hp1 HG01169.hp2 HG01515.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1198A>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 1198 | chr2 | 6897140 | ||||||
| chr2:6897301 | C | G | 1 | a0001c0001t0016 | 3 | HG02055.hp2 HG02717.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1359C>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 1359 | chr2 | 6897301 | ||||||
| chr2:6897337 | G | A | 1 | a0001c0007t0038 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1395G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 1395 | chr2 | 6897337 | ||||||
| chr2:6897386 | C | G | 1 | a0001c0001t0011 | 5 | HG00741.hp1 HG01943.hp2 HG02155.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1444C>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 1444 | chr2 | 6897386 | ||||||
| chr2:6897388 | T | A | 1 | a0001c0001t0028 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1446T>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 1446 | chr2 | 6897388 | ||||||
| chr2:6897833 | C | T | 1 | a0001c0001t0027 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1891C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 1891 | chr2 | 6897833 | ||||||
| chr2:6897890 | A | T | 5 | a0001c0001t0004 a0001c0001t0018 a0001c0001t0026 others(2): Show |
18 | HG01168.hp1 HG01169.hp2 HG01515.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1948A>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 1948 | chr2 | 6897890 | ||||||
| chr2:6897978 | G | C | 3 | a0001c0001t0005 a0001c0001t0024 a0001c0008t0025 |
13 | HG00323.hp2 HG01175.hp1 HG01255.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2036G>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 2036 | chr2 | 6897978 | ||||||
| chr2:6897989 | C | T | 3 | a0001c0001t0003 a0001c0001t0030 a0002c0005t0003 |
27 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2047C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 2047 | chr2 | 6897989 | ||||||
| chr2:6897994 | C | CA | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(7): Show |
56 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2072dupA | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 2073 | INFO_REALIGN_3_PRIME | chr2 | 6897994 | |||||
| chr2:6897994 | C | CAA | 7 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0021 others(4): Show |
22 | HG00280.hp1 HG01884.hp1 HG01981.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2071_*2072dupAA | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 2073 | INFO_REALIGN_3_PRIME | chr2 | 6897994 | |||||
| chr2:6897994 | C | CAAA | 4 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0031 others(1): Show |
14 | HG02145.hp2 HG02615.hp2 HG02717.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2070_*2072dupAAA | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 2073 | INFO_REALIGN_3_PRIME | chr2 | 6897994 | |||||
| chr2:6898050 | A | AAAGCCC | 2 | a0001c0001t0009 a0001c0001t0031 |
7 | HG02615.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2112_*2117dupCCCA others(2): Show |
RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 2118 | INFO_REALIGN_3_PRIME | chr2 | 6898050 | |||||
| chr2:6898127 | G | A | 3 | a0001c0001t0003 a0001c0001t0030 a0002c0005t0003 |
27 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2185G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 2185 | chr2 | 6898127 | ||||||
| chr2:6898232 | T | A | 1 | a0001c0001t0019 | 2 | HG03516.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2290T>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 6/6 | 2290 | chr2 | 6898232 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:6878284 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.346+138C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878284 | |||||||
| chr2:6878368 | G | A | 8 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0025 others(5): Show |
18 | HG01070.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.346+222G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878368 | |||||||
| chr2:6878456 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG01099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.346+310T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878456 | |||||||
| chr2:6878465 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0044 |
4 | HG02080.hp2 NA18947.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+319G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878465 | |||||||
| chr2:6878467 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+321G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878467 | |||||||
| chr2:6878563 | C | T | 1 | a0001c0003t0001g0116 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.346+417C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878563 | |||||||
| chr2:6878750 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(125): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.346+604C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878750 | |||||||
| chr2:6878948 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(112): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.346+802A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878948 | |||||||
| chr2:6878964 | C | T | 1 | a0001c0002t0035g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.346+818C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878964 | |||||||
| chr2:6878986 | A | G | 5 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0025 others(2): Show |
10 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.346+840A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878986 | |||||||
| chr2:6878997 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0010g0010 a0001c0001t0012g0010 |
8 | NA18946.hp2 NA18955.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.346+851A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6878997 | |||||||
| chr2:6879153 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.346+1007G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879153 | |||||||
| chr2:6879259 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.346+1113G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879259 | |||||||
| chr2:6879458 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.346+1312A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879458 | |||||||
| chr2:6879610 | T | G | 1 | a0002c0005t0003g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.346+1464T>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879610 | |||||||
| chr2:6879783 | T | C | 2 | a0001c0001t0006g0028 a0001c0001t0012g0028 |
2 | HG00280.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.346+1637T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879783 | |||||||
| chr2:6879821 | A | G | 1 | a0002c0005t0003g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.346+1675A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879821 | |||||||
| chr2:6879837 | T | C | 1 | a0001c0003t0001g0116 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.346+1691T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879837 | |||||||
| chr2:6879853 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0003g0062 a0001c0001t0023g0022 |
4 | HG00408.hp2 HG00597.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+1707G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879853 | |||||||
| chr2:6879924 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0009g0007 others(1): Show |
9 | HG02257.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.346+1778T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879924 | |||||||
| chr2:6879931 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.346+1785G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6879931 | |||||||
| chr2:6880172 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+2026G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880172 | |||||||
| chr2:6880289 | T | C | 1 | a0001c0001t0031g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.346+2143T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880289 | |||||||
| chr2:6880359 | G | A | 1 | a0001c0001t0013g0057 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.346+2213G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880359 | |||||||
| chr2:6880373 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.346+2227T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880373 | |||||||
| chr2:6880440 | C | G | 2 | a0001c0001t0006g0040 a0001c0001t0021g0040 |
2 | HG02109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.346+2294C>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880440 | |||||||
| chr2:6880558 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.346+2412C>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880558 | |||||||
| chr2:6880698 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.346+2552T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880698 | |||||||
| chr2:6880801 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.347-2570G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880801 | |||||||
| chr2:6880883 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.347-2488A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880883 | |||||||
| chr2:6880918 | A | C | 1 | a0001c0001t0001g0038 | 2 | HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.347-2453A>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880918 | |||||||
| chr2:6880939 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.347-2432A>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880939 | |||||||
| chr2:6880990 | A | G | 5 | a0001c0001t0017g0054 a0001c0002t0008g0016 a0001c0002t0017g0016 others(2): Show |
7 | HG02723.hp1 HG03130.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-2381A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6880990 | |||||||
| chr2:6881135 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.347-2236G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6881135 | |||||||
| chr2:6881218 | C | T | 1 | a0001c0001t0005g0006 | 6 | HG00323.hp2 HG01175.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.347-2153C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6881218 | |||||||
| chr2:6881406 | C | T | 1 | a0001c0001t0007g0020 | 3 | HG02615.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.347-1965C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6881406 | |||||||
| chr2:6881435 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.347-1936G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6881435 | |||||||
| chr2:6881658 | C | T | 2 | a0001c0002t0008g0016 a0001c0002t0017g0016 |
4 | HG02723.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-1713C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6881658 | |||||||
| chr2:6881760 | G | A | 1 | a0001c0001t0027g0068 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.347-1611G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6881760 | |||||||
| chr2:6881852 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-1519G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6881852 | |||||||
| chr2:6881907 | G | A | 1 | a0001c0001t0031g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.347-1464G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6881907 | |||||||
| chr2:6882065 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.347-1306G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6882065 | |||||||
| chr2:6882276 | CA | C | 2 | a0001c0002t0008g0016 a0001c0002t0017g0016 |
4 | HG02723.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-1088delA | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 6882276 | ||||||
| chr2:6882283 | A | G | 2 | a0001c0002t0008g0016 a0001c0002t0017g0016 |
4 | HG02723.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-1088A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6882283 | |||||||
| chr2:6882388 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(135): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.347-983T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6882388 | |||||||
| chr2:6882445 | TA | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(135): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.347-924delA | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 6882445 | ||||||
| chr2:6882700 | G | C | 1 | a0001c0002t0035g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.347-671G>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6882700 | |||||||
| chr2:6882742 | A | T | 1 | a0001c0001t0002g0113 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.347-629A>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6882742 | |||||||
| chr2:6882775 | C | T | 2 | a0001c0002t0008g0016 a0001c0002t0017g0016 |
4 | HG02723.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-596C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6882775 | |||||||
| chr2:6882921 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0070 a0001c0001t0002g0029 |
5 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-450T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6882921 | |||||||
| chr2:6882969 | AG | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0112 a0001c0001t0002g0111 others(1): Show |
10 | HG00140.hp2 HG01106.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-399delG | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 6882969 | ||||||
| chr2:6882971 | G | A | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
12 | HG02257.hp2 HG02258.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-400G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6882971 | |||||||
| chr2:6883058 | G | A | 1 | a0002c0005t0003g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.347-313G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6883058 | |||||||
| chr2:6883140 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.347-231G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6883140 | |||||||
| chr2:6883148 | C | A | 1 | a0001c0002t0035g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.347-223C>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 1/5 | chr2 | 6883148 | |||||||
| chr2:6883550 | G | A | 1 | a0001c0001t0006g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.508+18G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6883550 | |||||||
| chr2:6883586 | G | T | 1 | a0001c0001t0006g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.508+54G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6883586 | |||||||
| chr2:6883603 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.508+71C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6883603 | |||||||
| chr2:6883632 | G | A | 1 | a0001c0001t0010g0073 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.508+100G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6883632 | |||||||
| chr2:6883919 | C | T | 3 | a0001c0001t0006g0040 a0001c0001t0006g0109 a0001c0001t0021g0040 |
3 | HG01884.hp1 HG02109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.508+387C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6883919 | |||||||
| chr2:6883954 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0108 |
3 | HG00673.hp1 HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.508+422A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6883954 | |||||||
| chr2:6884041 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.508+509T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884041 | |||||||
| chr2:6884486 | A | G | 11 | a0001c0001t0003g0003 a0001c0001t0003g0062 a0001c0001t0003g0107 others(8): Show |
34 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.508+954A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884486 | |||||||
| chr2:6884494 | G | A | 1 | a0001c0001t0011g0011 | 5 | HG00741.hp1 HG01943.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+962G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884494 | |||||||
| chr2:6884589 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(119): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.508+1057A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884589 | |||||||
| chr2:6884682 | A | G | 5 | a0001c0001t0013g0035 a0001c0001t0017g0050 a0001c0001t0017g0054 others(2): Show |
8 | HG02258.hp1 HG02723.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.508+1150A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884682 | |||||||
| chr2:6884743 | G | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0076 others(11): Show |
30 | HG01168.hp1 HG01169.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.508+1211G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884743 | |||||||
| chr2:6884754 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.508+1222C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884754 | |||||||
| chr2:6884783 | C | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(130): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.508+1251C>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884783 | |||||||
| chr2:6884805 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.508+1273A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884805 | |||||||
| chr2:6884835 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.508+1303C>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884835 | |||||||
| chr2:6884882 | G | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0103 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.508+1350G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6884882 | |||||||
| chr2:6885044 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(83): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.508+1512C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885044 | |||||||
| chr2:6885107 | G | T | 1 | a0001c0001t0036g0102 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.508+1575G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885107 | |||||||
| chr2:6885140 | G | A | 1 | a0001c0007t0038g0078 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.508+1608G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885140 | |||||||
| chr2:6885219 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(76): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.508+1687G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885219 | |||||||
| chr2:6885228 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.508+1696T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885228 | |||||||
| chr2:6885277 | G | A | 1 | a0001c0001t0032g0083 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.509-1658G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885277 | |||||||
| chr2:6885449 | A | G | 7 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0025 others(4): Show |
12 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.509-1486A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885449 | |||||||
| chr2:6885628 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.509-1307A>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885628 | |||||||
| chr2:6885671 | G | A | 1 | a0001c0001t0007g0043 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.509-1264G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885671 | |||||||
| chr2:6885750 | TA | T | 15 | a0001c0001t0003g0003 a0001c0001t0003g0062 a0001c0001t0003g0107 others(12): Show |
45 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.509-1183delA | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 6885750 | ||||||
| chr2:6885821 | A | G | 1 | a0001c0001t0006g0081 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.509-1114A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885821 | |||||||
| chr2:6885866 | A | T | 1 | a0001c0001t0019g0027 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509-1069A>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885866 | |||||||
| chr2:6885925 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.509-1010C>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885925 | |||||||
| chr2:6885951 | C | T | 1 | a0001c0001t0001g0013 | 5 | HG01891.hp1 HG03041.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-984C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885951 | |||||||
| chr2:6885960 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.509-975C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6885960 | |||||||
| chr2:6886473 | A | G | 20 | a0001c0001t0001g0067 a0001c0001t0006g0009 a0001c0001t0006g0028 others(17): Show |
34 | HG00280.hp1 HG01099.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.509-462A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6886473 | |||||||
| chr2:6886827 | T | A | 17 | a0001c0001t0003g0003 a0001c0001t0003g0062 a0001c0001t0003g0107 others(14): Show |
47 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.509-108T>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 2/5 | chr2 | 6886827 | |||||||
| chr2:6887192 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(84): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.738+28T>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6887192 | |||||||
| chr2:6887532 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.738+368G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6887532 | |||||||
| chr2:6887740 | C | T | 2 | a0001c0001t0004g0008 a0004c0006t0004g0008 |
6 | HG02074.hp1 HG02135.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+576C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6887740 | |||||||
| chr2:6887820 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.738+656G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6887820 | |||||||
| chr2:6887964 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.738+800G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6887964 | |||||||
| chr2:6888006 | A | G | 6 | a0001c0001t0003g0003 a0001c0001t0003g0062 a0001c0001t0003g0107 others(3): Show |
25 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.738+842A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6888006 | |||||||
| chr2:6888183 | C | T | 1 | a0001c0001t0019g0027 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.738+1019C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6888183 | |||||||
| chr2:6888300 | A | G | 1 | a0001c0001t0007g0025 | 2 | HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.738+1136A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6888300 | |||||||
| chr2:6888305 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.738+1141G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6888305 | |||||||
| chr2:6888307 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(85): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.738+1143A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6888307 | |||||||
| chr2:6888391 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.738+1227C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6888391 | |||||||
| chr2:6888521 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(76): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.738+1357C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6888521 | |||||||
| chr2:6888573 | C | T | 7 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0025 others(4): Show |
12 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.738+1409C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6888573 | |||||||
| chr2:6889009 | A | T | 3 | a0001c0001t0008g0079 a0001c0001t0034g0080 a0001c0007t0038g0078 |
3 | HG02109.hp2 HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.739-1167A>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889009 | |||||||
| chr2:6889062 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.739-1114C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889062 | |||||||
| chr2:6889063 | G | A | 1 | a0001c0001t0002g0115 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.739-1113G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889063 | |||||||
| chr2:6889089 | T | G | 1 | a0001c0001t0001g0032 | 2 | HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.739-1087T>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889089 | |||||||
| chr2:6889154 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.739-1022T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889154 | |||||||
| chr2:6889249 | G | A | 7 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0025 others(4): Show |
12 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.739-927G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889249 | |||||||
| chr2:6889304 | T | C | 18 | a0001c0001t0001g0026 a0001c0001t0003g0003 a0001c0001t0003g0062 others(15): Show |
49 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.739-872T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889304 | |||||||
| chr2:6889352 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(71): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.739-824G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889352 | |||||||
| chr2:6889360 | A | G | 1 | a0001c0008t0025g0042 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.739-816A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889360 | |||||||
| chr2:6889427 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0030 |
6 | HG01168.hp2 HG01192.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.739-749C>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889427 | |||||||
| chr2:6889471 | C | T | 1 | a0001c0001t0022g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.739-705C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889471 | |||||||
| chr2:6889508 | T | G | 2 | a0001c0001t0008g0079 a0001c0001t0034g0080 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.739-668T>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889508 | |||||||
| chr2:6889545 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.739-631C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889545 | |||||||
| chr2:6889594 | C | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(68): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.739-582C>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889594 | |||||||
| chr2:6889851 | A | G | 1 | a0002c0005t0003g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.739-325A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 3/5 | chr2 | 6889851 | |||||||
| chr2:6890410 | C | T | 6 | a0001c0001t0003g0003 a0001c0001t0003g0062 a0001c0001t0003g0107 others(3): Show |
25 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.888+85C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6890410 | |||||||
| chr2:6890427 | G | C | 1 | a0001c0001t0002g0075 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.888+102G>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6890427 | |||||||
| chr2:6890539 | C | T | 2 | a0001c0004t0015g0019 a0002c0005t0015g0059 |
4 | HG02451.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.888+214C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6890539 | |||||||
| chr2:6890622 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.888+297A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6890622 | |||||||
| chr2:6890858 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0087 |
7 | HG01168.hp2 HG01192.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.888+533G>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6890858 | |||||||
| chr2:6890937 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.888+612T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6890937 | |||||||
| chr2:6891096 | A | G | 4 | a0001c0001t0013g0035 a0001c0001t0013g0057 a0001c0001t0013g0058 others(1): Show |
6 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.888+771A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891096 | |||||||
| chr2:6891111 | A | T | 16 | a0001c0001t0001g0067 a0001c0001t0006g0009 a0001c0001t0006g0028 others(13): Show |
25 | HG00280.hp1 HG01099.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.888+786A>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891111 | |||||||
| chr2:6891225 | A | C | 3 | a0001c0001t0013g0035 a0001c0001t0013g0057 a0001c0001t0013g0058 |
4 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.888+900A>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891225 | |||||||
| chr2:6891259 | A | G | 2 | a0001c0001t0008g0079 a0001c0001t0034g0080 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.888+934A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891259 | |||||||
| chr2:6891322 | T | C | 2 | a0001c0001t0008g0079 a0001c0001t0034g0080 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.888+997T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891322 | |||||||
| chr2:6891527 | G | C | 21 | a0001c0001t0001g0067 a0001c0001t0006g0009 a0001c0001t0006g0028 others(18): Show |
35 | HG00280.hp1 HG01099.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.888+1202G>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891527 | |||||||
| chr2:6891586 | T | C | 4 | a0001c0001t0013g0035 a0001c0001t0013g0057 a0001c0001t0013g0058 others(1): Show |
6 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.888+1261T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891586 | |||||||
| chr2:6891653 | G | C | 20 | a0001c0001t0001g0067 a0001c0001t0006g0009 a0001c0001t0006g0028 others(17): Show |
34 | HG00280.hp1 HG01099.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.888+1328G>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891653 | |||||||
| chr2:6891660 | G | T | 1 | a0001c0001t0003g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.888+1335G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891660 | |||||||
| chr2:6891747 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.888+1422C>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891747 | |||||||
| chr2:6891759 | C | G | 7 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0025 others(4): Show |
12 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.888+1434C>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891759 | |||||||
| chr2:6891796 | C | CA | 11 | a0001c0001t0002g0029 a0001c0001t0002g0075 a0001c0001t0008g0014 others(8): Show |
18 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.888+1480dupA | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 6891796 | ||||||
| chr2:6891869 | G | T | 1 | a0001c0001t0040g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.888+1544G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891869 | |||||||
| chr2:6891948 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG02129.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.888+1623T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6891948 | |||||||
| chr2:6892047 | A | C | 8 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0076 others(5): Show |
19 | HG01168.hp1 HG01169.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.889-1624A>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6892047 | |||||||
| chr2:6892167 | T | A | 1 | a0001c0001t0002g0095 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.889-1504T>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6892167 | |||||||
| chr2:6892238 | C | T | 7 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0025 others(4): Show |
12 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.889-1433C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6892238 | |||||||
| chr2:6892267 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(76): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.889-1404A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6892267 | |||||||
| chr2:6892487 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(64): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.889-1184T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6892487 | |||||||
| chr2:6892618 | C | T | 1 | a0001c0001t0001g0024 | 3 | NA18939.hp2 NA18954.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.889-1053C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6892618 | |||||||
| chr2:6892742 | CTGA | C | 12 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0076 others(9): Show |
24 | HG01168.hp1 HG01169.hp2 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.889-926_889-924del others(3): Show |
RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 6892742 | ||||||
| chr2:6892912 | G | A | 3 | a0001c0001t0002g0071 a0001c0001t0002g0096 a0001c0001t0002g0111 |
3 | NA19000.hp2 NA19007.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.889-759G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6892912 | |||||||
| chr2:6892929 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.889-742T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6892929 | |||||||
| chr2:6893052 | G | A | 6 | a0001c0001t0007g0015 a0001c0001t0007g0020 a0001c0001t0007g0025 others(3): Show |
11 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.889-619G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6893052 | |||||||
| chr2:6893180 | T | C | 1 | a0001c0001t0007g0025 | 2 | HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.889-491T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6893180 | |||||||
| chr2:6893246 | ACCCTTT | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(73): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.889-424_889-419del others(6): Show |
RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6893246 | |||||||
| chr2:6893457 | A | G | 3 | a0001c0001t0013g0057 a0001c0001t0013g0058 a0001c0001t0019g0027 |
4 | HG03453.hp2 HG03516.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-214A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6893457 | |||||||
| chr2:6893485 | A | C | 2 | a0001c0001t0013g0057 a0001c0001t0013g0058 |
2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.889-186A>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6893485 | |||||||
| chr2:6893543 | G | A | 1 | a0001c0001t0006g0031 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.889-128G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 4/5 | chr2 | 6893543 | |||||||
| chr2:6893803 | G | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0112 |
2 | NA18957.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.921+100G>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6893803 | |||||||
| chr2:6893856 | A | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0091 |
2 | NA18994.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.921+153A>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6893856 | |||||||
| chr2:6893869 | C | G | 2 | a0001c0001t0009g0007 a0001c0001t0031g0046 |
7 | HG02615.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.921+166C>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6893869 | |||||||
| chr2:6893902 | A | G | 19 | a0001c0001t0001g0067 a0001c0001t0006g0009 a0001c0001t0006g0028 others(16): Show |
33 | HG00280.hp1 HG01099.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.921+199A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6893902 | |||||||
| chr2:6893927 | G | A | 1 | a0001c0001t0004g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.921+224G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6893927 | |||||||
| chr2:6894027 | GT | G | 3 | a0001c0001t0013g0057 a0001c0001t0013g0058 a0001c0001t0019g0027 |
4 | HG03453.hp2 HG03516.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.921+326delT | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 6894027 | ||||||
| chr2:6894084 | G | A | 1 | a0001c0008t0025g0042 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.921+381G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6894084 | |||||||
| chr2:6894167 | T | C | 1 | a0001c0008t0025g0042 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.921+464T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6894167 | |||||||
| chr2:6894295 | CT | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(60): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.921+601delT | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 6894295 | ||||||
| chr2:6894312 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.921+609T>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6894312 | |||||||
| chr2:6894365 | T | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.921+662T>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6894365 | |||||||
| chr2:6894432 | ATACT | A | 3 | a0001c0001t0008g0014 a0001c0002t0008g0016 a0001c0002t0017g0016 |
8 | HG01070.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+734_921+737del others(4): Show |
RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 6894432 | ||||||
| chr2:6894571 | A | G | 1 | a0001c0001t0008g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.921+868A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6894571 | |||||||
| chr2:6894640 | A | G | 1 | a0001c0001t0002g0012 | 5 | HG02280.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.921+937A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6894640 | |||||||
| chr2:6895195 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.922-583C>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895195 | |||||||
| chr2:6895292 | A | G | 1 | a0001c0001t0013g0035 | 2 | HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.922-486A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895292 | |||||||
| chr2:6895302 | A | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(87): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.922-476A>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895302 | |||||||
| chr2:6895354 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.922-424T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895354 | |||||||
| chr2:6895366 | C | T | 2 | a0001c0004t0015g0019 a0002c0005t0015g0059 |
4 | HG02451.hp2 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.922-412C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895366 | |||||||
| chr2:6895470 | C | T | 1 | a0001c0007t0038g0078 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.922-308C>T | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895470 | |||||||
| chr2:6895535 | G | A | 1 | a0001c0001t0012g0105 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.922-243G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895535 | |||||||
| chr2:6895602 | A | G | 12 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0076 others(9): Show |
31 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.922-176A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895602 | |||||||
| chr2:6895624 | T | C | 15 | a0001c0001t0006g0009 a0001c0001t0006g0028 a0001c0001t0006g0031 others(12): Show |
24 | HG00280.hp1 HG01099.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.922-154T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895624 | |||||||
| chr2:6895633 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.922-145A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895633 | |||||||
| chr2:6895677 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.922-101A>G | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895677 | |||||||
| chr2:6895710 | T | C | 1 | a0001c0008t0025g0042 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.922-68T>C | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895710 | |||||||
| chr2:6895762 | G | A | 2 | a0001c0001t0013g0057 a0001c0001t0013g0058 |
2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.922-16G>A | RSAD2 | ENSG00000134321.13 | transcript | ENST00000382040.4 | protein_coding | 5/5 | chr2 | 6895762 |