Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 58528 |
| ensemblid | ENSG00000025039.15 |
| hgncid | 19903 |
| symbol | RRAGD |
| name | Ras related GTP binding D |
| refseq_nuc | NM_021244.5 |
| refseq_prot | NP_067067.1 |
| ensembl_nuc | ENST00000369415.9 |
| ensembl_prot | ENSP00000358423.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 89364616 |
| end | 89412273 |
| strand | - |
| ver | v1.2 |
| region | chr6:89364616-89412273 |
| region5000 | chr6:89359616-89417273 |
| regionname0 | RRAGD_chr6_89364616_89412273 |
| regionname5000 | RRAGD_chr6_89359616_89417273 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 400 | 370 | 93 | 66 | 154 | 17 | 38 | 120 | RRAGD_chr6_89359616_89417273 | RRAGD | MSQVL others(395): Show |
chr6 | 89359616 | 89417273 |
| a0002 | 0/0 | 400 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | MSQVL others(395): Show |
chr6 | 89359616 | 89417273 |
| a0003 | 0/0 | 400 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | MSQVL others(395): Show |
chr6 | 89359616 | 89417273 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1200 | 360 | 86 | 66 | 154 | 16 | 36 | RRAGD_chr6_89359616_89417273 | RRAGD | ATGAG others(1195): Show |
chr6 | 89359616 | 89417273 | ||
| a0001c0002 | 0/0 | 1200 | 7 | 6 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | ATGAG others(1195): Show |
chr6 | 89359616 | 89417273 | ||
| a0001c0003 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | ATGAG others(1195): Show |
chr6 | 89359616 | 89417273 | ||
| a0001c0004 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | ATGAG others(1195): Show |
chr6 | 89359616 | 89417273 | ||
| a0001c0005 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | ATGAG others(1195): Show |
chr6 | 89359616 | 89417273 | ||
| a0002c0006 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | ATGAG others(1195): Show |
chr6 | 89359616 | 89417273 | ||
| a0003c0007 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | ATGAG others(1195): Show |
chr6 | 89359616 | 89417273 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4923 | 73 | 9 | 20 | 35 | 4 | 5 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0002 | 0/0 | 4924 | 51 | 0 | 6 | 44 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0003 | 0/1 | 4922 | 48 | 1 | 4 | 32 | 1 | 9 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0004 | 0/0 | 4927 | 30 | 15 | 5 | 7 | 2 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0005 | 0/0 | 4923 | 11 | 0 | 4 | 1 | 3 | 3 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0006 | 0/0 | 4923 | 10 | 3 | 2 | 0 | 1 | 4 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0007 | 0/0 | 4926 | 10 | 9 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4921): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0008 | 0/0 | 4926 | 10 | 2 | 3 | 5 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4921): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0009 | 0/0 | 4927 | 9 | 0 | 1 | 3 | 2 | 3 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0010 | 0/0 | 4920 | 7 | 0 | 0 | 7 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4915): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0011 | 0/0 | 4923 | 7 | 6 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0012 | 0/0 | 4928 | 7 | 7 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4923): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0013 | 1/0 | 4923 | 6 | 0 | 2 | 0 | 2 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0014 | 0/0 | 4922 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0015 | 0/0 | 4926 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4921): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0016 | 0/0 | 4924 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0017 | 0/0 | 4921 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4916): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0018 | 0/0 | 4923 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0019 | 0/0 | 4927 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0020 | 0/0 | 4922 | 3 | 0 | 2 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0022 | 0/0 | 4925 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4920): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0023 | 0/0 | 4926 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4921): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0024 | 0/0 | 4927 | 3 | 0 | 3 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0025 | 0/0 | 4927 | 3 | 0 | 1 | 0 | 1 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0026 | 0/0 | 4924 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0027 | 0/0 | 4922 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0028 | 0/0 | 4922 | 2 | 0 | 1 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0029 | 0/0 | 4923 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0030 | 0/0 | 4927 | 2 | 0 | 1 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0031 | 0/0 | 4928 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4923): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0032 | 0/0 | 4919 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4914): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0033 | 0/0 | 4924 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0034 | 0/0 | 4922 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0035 | 0/0 | 4923 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0037 | 0/0 | 4922 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0038 | 0/0 | 4924 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0041 | 0/0 | 4922 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0042 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0043 | 0/0 | 4921 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4916): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0044 | 0/0 | 4922 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0045 | 0/0 | 4922 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0046 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0047 | 0/0 | 4924 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0048 | 0/0 | 4924 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0049 | 0/0 | 4924 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0050 | 0/0 | 4924 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0051 | 0/0 | 4924 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4919): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0052 | 0/0 | 4920 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4915): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0053 | 0/0 | 4922 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0054 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0055 | 0/0 | 4927 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0057 | 0/0 | 4926 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4921): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0058 | 0/0 | 4927 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0059 | 0/0 | 4927 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0060 | 0/0 | 4926 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4921): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0061 | 0/0 | 4927 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0062 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4923): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0063 | 0/0 | 4925 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4920): Show |
chr6 | 89359616 | 89417273 |
| a0001c0001t0064 | 0/0 | 4927 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0002t0019 | 0/0 | 4927 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0002t0021 | 0/0 | 4926 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4921): Show |
chr6 | 89359616 | 89417273 |
| a0001c0002t0040 | 0/0 | 4922 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0002t0056 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4921): Show |
chr6 | 89359616 | 89417273 |
| a0001c0003t0004 | 0/0 | 4927 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4922): Show |
chr6 | 89359616 | 89417273 |
| a0001c0004t0039 | 0/0 | 4922 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4917): Show |
chr6 | 89359616 | 89417273 |
| a0001c0005t0036 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0002c0006t0001 | 0/0 | 4923 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| a0003c0007t0001 | 0/0 | 4923 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | AGTCT others(4918): Show |
chr6 | 89359616 | 89417273 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0005g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0005g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0006g0002 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0007g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0008g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0009g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0009g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0009g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0009g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0009g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0009g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0009g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0009g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0010g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0010g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0011g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0011g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0011g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0011g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0012g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0012g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0012g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0012g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0012g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0012g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0013g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0013g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0013g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0013g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0013g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0014g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0015g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0015g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0015g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0015g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0015g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0016g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0016g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0016g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0016g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0017g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0017g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0017g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0017g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0018g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0018g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0018g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0018g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0019g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0019g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0020g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0020g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0020g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0022g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0022g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0022g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0023g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0023g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0023g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0024g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0024g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0024g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0025g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0025g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0025g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0026g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0026g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0027g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0027g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0028g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0028g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0029g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0029g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0030g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0030g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0031g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0031g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0032g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0033g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0034g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0035g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0037g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0038g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0041g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0042g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0043g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0044g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0045g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0046g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0047g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0048g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0049g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0050g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0051g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0052g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0053g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0054g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0055g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0057g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0058g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0059g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0060g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0061g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0062g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0063g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0001t0064g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0002t0019g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0002t0019g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0002t0021g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0002t0021g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0002t0021g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0002t0040g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0002t0056g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0003t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0004t0039g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0001c0005t0036g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0002c0006t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| a0003c0007t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0002 | EUR | GBR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00140 | hp1 | a0001 | c0001 | t0009 | g0303 | EUR | GBR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0239 | EUR | FIN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00280 | hp2 | a0002 | c0006 | t0001 | g0207 | EUR | FIN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0291 | EUR | FIN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00621 | hp2 | a0001 | c0001 | t0051 | g0136 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0308 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0297 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00738 | hp1 | a0001 | c0001 | t0011 | g0089 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00741 | hp1 | a0001 | c0001 | t0061 | g0325 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01069 | hp2 | a0001 | c0001 | t0034 | g0071 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01071 | hp2 | a0001 | c0001 | t0035 | g0070 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0290 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0274 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01099 | hp2 | a0001 | c0001 | t0041 | g0082 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01106 | hp1 | a0001 | c0001 | t0024 | g0338 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0326 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0101 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0240 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01168 | hp2 | a0001 | c0001 | t0024 | g0310 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01169 | hp1 | a0001 | c0001 | t0027 | g0243 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0256 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01192 | hp2 | a0001 | c0001 | t0013 | g0076 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01243 | hp2 | a0001 | c0001 | t0055 | g0296 | AMR | PUR | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01255 | hp2 | a0001 | c0001 | t0045 | g0077 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01257 | hp2 | a0001 | c0001 | t0027 | g0085 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01261 | hp1 | a0001 | c0001 | t0020 | g0083 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01346 | hp1 | a0001 | c0001 | t0009 | g0018 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01358 | hp1 | a0001 | c0001 | t0028 | g0221 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0242 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01433 | hp1 | a0001 | c0001 | t0020 | g0237 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01433 | hp2 | a0001 | c0001 | t0025 | g0342 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0017 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01516 | hp1 | a0001 | c0001 | t0009 | g0289 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01516 | hp2 | a0001 | c0001 | t0013 | g0010 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0241 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01517 | hp2 | a0001 | c0001 | t0013 | g0010 | EUR | IBS | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01884 | hp1 | a0001 | c0001 | t0059 | g0320 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0285 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01943 | hp2 | a0001 | c0001 | t0049 | g0225 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01978 | hp2 | a0001 | c0001 | t0024 | g0263 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01993 | hp2 | a0001 | c0001 | t0013 | g0078 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02040 | hp2 | a0001 | c0001 | t0050 | g0126 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02055 | hp1 | a0001 | c0001 | t0019 | g0337 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02056 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02071 | hp2 | a0001 | c0001 | t0008 | g0259 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02129 | hp1 | a0001 | c0001 | t0062 | g0286 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0257 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02132 | hp2 | a0001 | c0001 | t0008 | g0258 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0251 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02145 | hp2 | a0001 | c0001 | t0064 | g0343 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | CDX | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0272 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02258 | hp2 | a0001 | c0002 | t0021 | g0335 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02293 | hp1 | a0001 | c0001 | t0030 | g0304 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02451 | hp1 | a0001 | c0001 | t0022 | g0311 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0253 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02523 | hp2 | a0001 | c0001 | t0010 | g0022 | EAS | KHV | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0312 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0306 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0017 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0091 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0270 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0284 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0093 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0094 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0264 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0268 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02723 | hp1 | a0001 | c0002 | t0021 | g0333 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0105 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0088 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02738 | hp1 | a0001 | c0001 | t0030 | g0262 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0271 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0323 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02886 | hp1 | a0001 | c0001 | t0063 | g0269 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0336 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0315 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02895 | hp2 | a0001 | c0001 | t0016 | g0279 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02896 | hp2 | a0001 | c0001 | t0022 | g0249 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02897 | hp1 | a0001 | c0001 | t0016 | g0277 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02897 | hp2 | a0001 | c0001 | t0022 | g0250 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02922 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0265 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0329 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02965 | hp2 | a0001 | c0001 | t0015 | g0254 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02970 | hp2 | a0001 | c0001 | t0015 | g0252 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0328 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0280 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03041 | hp2 | a0001 | c0001 | t0031 | g0267 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0327 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03130 | hp1 | a0001 | c0001 | t0023 | g0247 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0095 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03195 | hp2 | a0001 | c0002 | t0019 | g0332 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03209 | hp1 | a0001 | c0002 | t0021 | g0331 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0035 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03225 | hp1 | a0001 | c0001 | t0026 | g0100 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03225 | hp2 | a0003 | c0007 | t0001 | g0218 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03239 | hp2 | a0001 | c0001 | t0042 | g0206 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0321 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03453 | hp2 | a0001 | c0001 | t0043 | g0032 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03486 | hp1 | a0001 | c0001 | t0052 | g0090 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0147 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0339 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0275 | AFR | ESN | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0314 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03579 | hp1 | a0001 | c0004 | t0039 | g0235 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03579 | hp2 | a0001 | c0002 | t0019 | g0330 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03669 | hp1 | a0001 | c0001 | t0060 | g0309 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03688 | hp2 | a0001 | c0001 | t0038 | g0068 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0079 | SAS | PJL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03831 | hp1 | a0001 | c0001 | t0046 | g0208 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03831 | hp2 | a0001 | c0001 | t0047 | g0086 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03834 | hp1 | a0001 | c0001 | t0009 | g0302 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03834 | hp2 | a0001 | c0001 | t0054 | g0244 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04115 | hp1 | a0001 | c0001 | t0009 | g0295 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0301 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04184 | hp2 | a0001 | c0001 | t0025 | g0341 | SAS | BEB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04199 | hp1 | a0001 | c0003 | t0004 | g0245 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0102 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04204 | hp1 | a0001 | c0005 | t0036 | g0069 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0087 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG04228 | hp2 | a0001 | c0001 | t0009 | g0299 | SAS | STU | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18522 | hp1 | a0001 | c0001 | t0023 | g0246 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0319 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18906 | hp2 | a0001 | c0001 | t0037 | g0097 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18944 | hp2 | a0001 | c0001 | t0028 | g0209 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18949 | hp2 | a0001 | c0001 | t0010 | g0026 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18951 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18959 | hp1 | a0001 | c0001 | t0017 | g0170 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18959 | hp2 | a0001 | c0001 | t0018 | g0142 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18963 | hp2 | a0001 | c0001 | t0010 | g0023 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18965 | hp1 | a0001 | c0001 | t0053 | g0226 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18967 | hp2 | a0001 | c0001 | t0018 | g0159 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18969 | hp1 | a0001 | c0001 | t0044 | g0198 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18974 | hp1 | a0001 | c0001 | t0048 | g0230 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18975 | hp1 | a0001 | c0001 | t0010 | g0024 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18982 | hp2 | a0001 | c0001 | t0009 | g0287 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18985 | hp1 | a0001 | c0001 | t0010 | g0028 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18993 | hp2 | a0001 | c0001 | t0057 | g0292 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA18995 | hp2 | a0001 | c0001 | t0009 | g0018 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19002 | hp1 | a0001 | c0001 | t0032 | g0025 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19002 | hp2 | a0001 | c0001 | t0009 | g0307 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19007 | hp1 | a0001 | c0001 | t0010 | g0029 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0324 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0255 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19043 | hp2 | a0001 | c0001 | t0023 | g0248 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19054 | hp1 | a0001 | c0001 | t0017 | g0163 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19060 | hp1 | a0001 | c0001 | t0029 | g0190 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19065 | hp1 | a0001 | c0001 | t0018 | g0125 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19067 | hp1 | a0001 | c0001 | t0017 | g0167 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19068 | hp1 | a0001 | c0001 | t0018 | g0114 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19076 | hp1 | a0001 | c0001 | t0033 | g0030 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19083 | hp2 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19089 | hp1 | a0001 | c0001 | t0029 | g0184 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19089 | hp2 | a0001 | c0001 | t0017 | g0062 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0096 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA19240 | hp2 | a0001 | c0001 | t0026 | g0099 | AFR | YRI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20129 | hp1 | a0001 | c0001 | t0016 | g0276 | AFR | ASW | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20752 | hp1 | a0001 | c0001 | t0025 | g0340 | EUR | TSI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0294 | EUR | TSI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20805 | hp1 | a0001 | c0002 | t0040 | g0031 | EUR | TSI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | TSI | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20905 | hp1 | a0001 | c0001 | t0020 | g0081 | SAS | GIH | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | GIH | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0084 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0313 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02109 | hp2 | a0001 | c0001 | t0016 | g0278 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02486 | hp1 | a0001 | c0001 | t0058 | g0317 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0037 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG02559 | hp2 | a0001 | c0001 | t0011 | g0092 | AFR | ACB | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG03471 | hp2 | a0001 | c0001 | t0031 | g0266 | AFR | MSL | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | USA | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | USA | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20300 | hp1 | a0001 | c0002 | t0056 | g0334 | AFR | USA | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | USA | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0146 | REF | REF | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0080 | REF | REF | RRAGD_chr6_89359616_89417273 | RRAGD | chr6 | 89359616 | 89417273 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:89368154 | C | G | 1 | a0003 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1105G>C | p.Glu369Gln | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1385/4923 | 1105/1203 | 369/400 | chr6 | 89368154 | |||
| chr6:89372512 | C | T | 1 | a0002 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.976G>A | p.Val326Met | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/7 | 1256/4923 | 976/1203 | 326/400 | chr6 | 89372512 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:89377751 | A | G | 1 | a0001c0005 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.822T>C | p.Asp274Asp | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/7 | 1102/4923 | 822/1203 | 274/400 | chr6 | 89377751 | |||
| chr6:89380302 | A | G | 1 | a0001c0004 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.510T>C | p.Thr170Thr | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/7 | 790/4923 | 510/1203 | 170/400 | chr6 | 89380302 | |||
| chr6:89380305 | A | G | 1 | a0001c0002 | 7 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(4): Show |
synonymous_variant | LOW | c.507T>C | p.Asn169Asn | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/7 | 787/4923 | 507/1203 | 169/400 | chr6 | 89380305 | |||
| chr6:89411928 | C | T | 1 | a0001c0003 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.66G>A | p.Glu22Glu | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 346/4923 | 66/1203 | 22/400 | chr6 | 89411928 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:89364805 | C | A | 1 | a0001c0001t0046 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3251G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 3251 | chr6 | 89364805 | ||||||
| chr6:89365315 | T | C | 1 | a0001c0004t0039 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2741A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2741 | chr6 | 89365315 | ||||||
| chr6:89365564 | T | A | 2 | a0001c0001t0029 a0001c0001t0044 |
3 | NA18969.hp1 NA19060.hp1 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2492A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2492 | chr6 | 89365564 | ||||||
| chr6:89365640 | A | G | 51 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(48): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*2416T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2416 | chr6 | 89365640 | ||||||
| chr6:89365928 | G | C | 7 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0018 others(4): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2128C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2128 | chr6 | 89365928 | ||||||
| chr6:89365987 | G | C | 8 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0018 others(5): Show |
70 | HG00438.hp1 HG01261.hp2 HG01891.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2069C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2069 | chr6 | 89365987 | ||||||
| chr6:89365987 | G | T | 1 | a0001c0001t0051 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2069C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2069 | chr6 | 89365987 | ||||||
| chr6:89365994 | G | A | 1 | a0001c0002t0040 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2062C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2062 | chr6 | 89365994 | ||||||
| chr6:89365998 | TG | T | 1 | a0001c0001t0015 | 5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2057delC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 2057 | chr6 | 89365998 | ||||||
| chr6:89366077 | A | C | 8 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0018 others(5): Show |
68 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1979T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1979 | chr6 | 89366077 | ||||||
| chr6:89366112 | A | C | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*1944T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1944 | chr6 | 89366112 | ||||||
| chr6:89366246 | G | A | 1 | a0001c0001t0058 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1810C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1810 | chr6 | 89366246 | ||||||
| chr6:89366388 | C | T | 3 | a0001c0001t0007 a0001c0001t0014 a0001c0002t0040 |
16 | HG01109.hp1 HG02257.hp1 HG02486.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1668G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1668 | chr6 | 89366388 | ||||||
| chr6:89366400 | T | G | 6 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0020 others(3): Show |
21 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1656A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1656 | chr6 | 89366400 | ||||||
| chr6:89366439 | G | A | 5 | a0001c0001t0016 a0001c0001t0022 a0001c0001t0043 others(2): Show |
11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1617C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1617 | chr6 | 89366439 | ||||||
| chr6:89366525 | T | TA | 10 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0031 others(7): Show |
67 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1530dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1530 | chr6 | 89366525 | ||||||
| chr6:89366525 | TA | T | 33 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(30): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*1530delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1530 | chr6 | 89366525 | ||||||
| chr6:89366525 | TAA | T | 6 | a0001c0001t0017 a0001c0001t0032 a0001c0001t0034 others(3): Show |
11 | HG01069.hp2 HG02258.hp2 HG02723.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1529_*1530delTT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1529 | chr6 | 89366525 | ||||||
| chr6:89366576 | T | A | 5 | a0001c0001t0016 a0001c0001t0022 a0001c0001t0043 others(2): Show |
11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1480A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1480 | chr6 | 89366576 | ||||||
| chr6:89366622 | TA | T | 7 | a0001c0001t0016 a0001c0001t0022 a0001c0001t0023 others(4): Show |
15 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1433delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1433 | chr6 | 89366622 | ||||||
| chr6:89366665 | C | T | 20 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 others(17): Show |
78 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1391G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1391 | chr6 | 89366665 | ||||||
| chr6:89366851 | G | A | 7 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0026 others(4): Show |
21 | HG00099.hp1 HG01109.hp2 HG01123.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1205C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1205 | chr6 | 89366851 | ||||||
| chr6:89366915 | A | G | 8 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0018 others(5): Show |
68 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1141T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1141 | chr6 | 89366915 | ||||||
| chr6:89366935 | G | A | 1 | a0001c0001t0059 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1121C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1121 | chr6 | 89366935 | ||||||
| chr6:89366951 | A | T | 21 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 others(18): Show |
83 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1105T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1105 | chr6 | 89366951 | ||||||
| chr6:89366966 | G | A | 5 | a0001c0001t0009 a0001c0001t0030 a0001c0001t0034 others(2): Show |
14 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1090C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1090 | chr6 | 89366966 | ||||||
| chr6:89367022 | C | T | 1 | a0001c0001t0011 | 7 | HG00738.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1034G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1034 | chr6 | 89367022 | ||||||
| chr6:89367040 | A | G | 1 | a0001c0002t0056 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1016T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 1016 | chr6 | 89367040 | ||||||
| chr6:89367135 | A | G | 1 | a0001c0001t0050 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*921T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 921 | chr6 | 89367135 | ||||||
| chr6:89367174 | A | G | 5 | a0001c0001t0016 a0001c0001t0022 a0001c0001t0043 others(2): Show |
11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*882T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 882 | chr6 | 89367174 | ||||||
| chr6:89367265 | C | T | 5 | a0001c0001t0009 a0001c0001t0030 a0001c0001t0034 others(2): Show |
14 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*791G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 791 | chr6 | 89367265 | ||||||
| chr6:89367267 | C | T | 5 | a0001c0001t0009 a0001c0001t0030 a0001c0001t0034 others(2): Show |
14 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*789G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 789 | chr6 | 89367267 | ||||||
| chr6:89367269 | C | T | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 787 | chr6 | 89367269 | ||||||
| chr6:89367274 | G | T | 5 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0010 others(2): Show |
69 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*782C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 782 | chr6 | 89367274 | ||||||
| chr6:89367401 | G | A | 1 | a0001c0001t0055 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*655C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 655 | chr6 | 89367401 | ||||||
| chr6:89367419 | G | A | 1 | a0001c0001t0014 | 5 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*637C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 637 | chr6 | 89367419 | ||||||
| chr6:89367423 | C | T | 2 | a0001c0001t0030 a0001c0001t0055 |
3 | HG01243.hp2 HG02293.hp1 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*633G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 633 | chr6 | 89367423 | ||||||
| chr6:89367712 | G | A | 7 | a0001c0001t0002 a0001c0001t0018 a0001c0001t0033 others(4): Show |
60 | HG00438.hp1 HG00621.hp2 HG01099.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*344C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 344 | chr6 | 89367712 | ||||||
| chr6:89367837 | A | G | 7 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0020 others(4): Show |
22 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*219T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 219 | chr6 | 89367837 | ||||||
| chr6:89367928 | A | AT | 21 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 others(18): Show |
79 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*127dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 127 | chr6 | 89367928 | ||||||
| chr6:89367928 | AT | A | 4 | a0001c0001t0016 a0001c0001t0052 a0001c0001t0053 others(1): Show |
8 | HG02109.hp2 HG02886.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*127delA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 7/7 | 127 | chr6 | 89367928 | ||||||
| chr6:89412025 | C | G | 1 | a0001c0001t0033 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 32 | chr6 | 89412025 | ||||||
| chr6:89412231 | G | A | 2 | a0001c0001t0025 a0001c0001t0064 |
4 | HG01433.hp2 HG02145.hp2 HG04184.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-238C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 238 | chr6 | 89412231 | ||||||
| chr6:89412235 | G | A | 1 | a0001c0001t0054 | 1 | HG03834.hp2 | 5_prime_UTR_variant | MODIFIER | c.-242C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 242 | chr6 | 89412235 | ||||||
| chr6:89412257 | G | GGAGA | 27 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(24): Show |
110 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-268_-265dupTCTC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 265 | chr6 | 89412257 | ||||||
| chr6:89412257 | GGA | G | 2 | a0001c0001t0010 a0001c0001t0032 |
8 | HG02056.hp2 HG02523.hp2 NA18949.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-266_-265delTC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/7 | 265 | chr6 | 89412257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:89368242 | C | T | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1052-35G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368242 | |||||||
| chr6:89368320 | G | A | 9 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0271 others(6): Show |
10 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1052-113C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368320 | |||||||
| chr6:89368330 | G | T | 77 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(74): Show |
81 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(78): Show |
intron_variant | MODIFIER | c.1052-123C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368330 | |||||||
| chr6:89368430 | G | A | 11 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(8): Show |
11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1052-223C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368430 | |||||||
| chr6:89368432 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1052-225A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368432 | |||||||
| chr6:89368617 | G | C | 11 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(8): Show |
11 | HG00438.hp2 HG01515.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1052-410C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368617 | |||||||
| chr6:89368683 | T | C | 32 | a0001c0001t0005g0011 a0001c0001t0005g0017 a0001c0001t0005g0087 others(29): Show |
36 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1052-476A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368683 | |||||||
| chr6:89368735 | G | T | 1 | a0001c0001t0024g0338 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1052-528C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368735 | |||||||
| chr6:89368815 | G | A | 78 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(75): Show |
82 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(79): Show |
intron_variant | MODIFIER | c.1052-608C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89368815 | |||||||
| chr6:89369021 | T | G | 1 | a0001c0001t0019g0337 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1052-814A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369021 | |||||||
| chr6:89369021 | TTCTA | T | 18 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0271 others(15): Show |
20 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1052-818_1052-815d others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369021 | |||||||
| chr6:89369050 | C | T | 4 | a0001c0001t0022g0249 a0001c0001t0022g0250 a0001c0001t0022g0311 others(1): Show |
4 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1052-843G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369050 | |||||||
| chr6:89369093 | C | A | 11 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(8): Show |
11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1052-886G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369093 | |||||||
| chr6:89369134 | G | A | 2 | a0001c0001t0016g0278 a0001c0001t0016g0280 |
2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1052-927C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369134 | |||||||
| chr6:89369495 | C | T | 139 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(136): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1052-1288G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369495 | |||||||
| chr6:89369508 | G | T | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1052-1301C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369508 | |||||||
| chr6:89369509 | C | T | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1052-1302G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369509 | |||||||
| chr6:89369827 | T | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.1052-1620A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89369827 | |||||||
| chr6:89370039 | C | T | 11 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(8): Show |
11 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1052-1832G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370039 | |||||||
| chr6:89370040 | G | A | 6 | a0001c0001t0020g0081 a0001c0001t0020g0083 a0001c0001t0020g0237 others(3): Show |
6 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1052-1833C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370040 | |||||||
| chr6:89370204 | A | C | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1052-1997T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370204 | |||||||
| chr6:89370409 | A | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.1051+2028T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370409 | |||||||
| chr6:89370498 | C | T | 1 | a0001c0001t0004g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1051+1939G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370498 | |||||||
| chr6:89370578 | A | G | 7 | a0001c0001t0011g0089 a0001c0001t0011g0091 a0001c0001t0011g0092 others(4): Show |
7 | HG00738.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+1859T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370578 | |||||||
| chr6:89370671 | C | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(62): Show |
69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.1051+1766G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370671 | |||||||
| chr6:89370871 | T | C | 1 | a0001c0001t0015g0253 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1051+1566A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370871 | |||||||
| chr6:89370928 | A | G | 1 | a0001c0001t0011g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1051+1509T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370928 | |||||||
| chr6:89370966 | TAAAC | T | 33 | a0001c0001t0004g0261 a0001c0001t0004g0273 a0001c0001t0004g0274 others(30): Show |
34 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.1051+1467_1051+147 others(8): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89370966 | |||||||
| chr6:89371098 | A | G | 1 | a0001c0001t0062g0286 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1051+1339T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371098 | |||||||
| chr6:89371209 | C | G | 65 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(62): Show |
69 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1051+1228G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371209 | |||||||
| chr6:89371288 | A | G | 1 | a0001c0001t0005g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1051+1149T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371288 | |||||||
| chr6:89371411 | C | T | 66 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(63): Show |
71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1051+1026G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371411 | |||||||
| chr6:89371497 | G | C | 1 | a0001c0001t0017g0062 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1051+940C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371497 | |||||||
| chr6:89371653 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1051+784G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89371653 | |||||||
| chr6:89372068 | C | T | 1 | a0001c0001t0003g0040 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1051+369G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89372068 | |||||||
| chr6:89372242 | C | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0205 a0001c0001t0024g0310 others(1): Show |
4 | HG00741.hp2 HG01168.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051+195G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89372242 | |||||||
| chr6:89372271 | G | A | 51 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(48): Show |
53 | HG00438.hp2 HG00673.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.1051+166C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 6/6 | chr6 | 89372271 | |||||||
| chr6:89372964 | A | T | 2 | a0001c0001t0004g0261 a0001c0001t0004g0273 |
2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.903-379T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89372964 | |||||||
| chr6:89373024 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.903-439T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373024 | |||||||
| chr6:89373026 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.903-441T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373026 | |||||||
| chr6:89373441 | C | G | 2 | a0001c0001t0031g0266 a0001c0001t0031g0267 |
2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.903-856G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373441 | |||||||
| chr6:89373468 | A | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.903-883T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373468 | |||||||
| chr6:89373537 | G | A | 6 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(3): Show |
6 | HG02109.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.903-952C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373537 | |||||||
| chr6:89373568 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.903-983T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373568 | |||||||
| chr6:89373617 | C | CA | 12 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0271 others(9): Show |
13 | HG00741.hp1 HG02257.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.903-1033dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373617 | |||||||
| chr6:89373617 | CA | C | 25 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0219 others(22): Show |
25 | HG01255.hp2 HG01496.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.903-1033delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373617 | |||||||
| chr6:89373617 | CAA | C | 61 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(58): Show |
65 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(62): Show |
intron_variant | MODIFIER | c.903-1034_903-1033d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373617 | |||||||
| chr6:89373672 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.903-1087G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373672 | |||||||
| chr6:89373682 | T | G | 1 | a0001c0001t0005g0239 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.903-1097A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373682 | |||||||
| chr6:89373701 | ATTTCT | A | 16 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(13): Show |
16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.903-1121_903-1117d others(7): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373701 | |||||||
| chr6:89373739 | C | T | 11 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0271 others(8): Show |
12 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.903-1154G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373739 | |||||||
| chr6:89373773 | G | A | 1 | a0001c0001t0011g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.903-1188C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373773 | |||||||
| chr6:89373782 | CAG | C | 27 | a0001c0001t0005g0017 a0001c0001t0005g0239 a0001c0001t0005g0240 others(24): Show |
30 | HG00280.hp1 HG01099.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.903-1199_903-1198d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89373782 | |||||||
| chr6:89374338 | G | T | 1 | a0001c0001t0003g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.903-1753C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374338 | |||||||
| chr6:89374375 | T | G | 1 | a0001c0002t0019g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.903-1790A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374375 | |||||||
| chr6:89374418 | T | G | 2 | a0001c0001t0022g0249 a0001c0001t0022g0250 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.903-1833A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374418 | |||||||
| chr6:89374590 | C | T | 66 | a0001c0001t0001g0014 a0001c0001t0003g0007 a0001c0001t0003g0008 others(63): Show |
71 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.903-2005G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374590 | |||||||
| chr6:89374607 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.903-2022C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374607 | |||||||
| chr6:89374652 | C | A | 1 | a0001c0001t0028g0209 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.903-2067G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374652 | |||||||
| chr6:89374654 | C | T | 1 | a0001c0001t0009g0302 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.903-2069G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374654 | |||||||
| chr6:89374706 | G | T | 65 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(62): Show |
69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.903-2121C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374706 | |||||||
| chr6:89374749 | T | C | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.903-2164A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374749 | |||||||
| chr6:89374770 | G | GTT | 64 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(61): Show |
68 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(65): Show |
intron_variant | MODIFIER | c.903-2187_903-2186d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374770 | |||||||
| chr6:89374798 | A | C | 1 | a0001c0001t0003g0061 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.903-2213T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374798 | |||||||
| chr6:89374896 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.903-2311G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374896 | |||||||
| chr6:89374905 | T | G | 9 | a0001c0001t0014g0006 a0001c0001t0014g0035 a0001c0001t0014g0036 others(6): Show |
10 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.903-2320A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374905 | |||||||
| chr6:89374991 | T | C | 1 | a0001c0001t0045g0077 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.903-2406A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89374991 | |||||||
| chr6:89375041 | T | C | 5 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.903-2456A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375041 | |||||||
| chr6:89375170 | C | A | 4 | a0001c0001t0002g0149 a0001c0001t0002g0151 a0001c0001t0002g0153 others(1): Show |
4 | HG02015.hp1 NA18953.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.902+2501G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375170 | |||||||
| chr6:89375206 | G | A | 1 | a0001c0001t0004g0293 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.902+2465C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375206 | |||||||
| chr6:89375234 | T | C | 3 | a0001c0001t0022g0249 a0001c0001t0022g0250 a0001c0001t0022g0311 |
3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.902+2437A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375234 | |||||||
| chr6:89375384 | C | T | 2 | a0001c0001t0010g0024 a0001c0001t0010g0027 |
2 | HG02056.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.902+2287G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375384 | |||||||
| chr6:89375432 | C | T | 3 | a0001c0001t0004g0021 a0001c0001t0004g0318 a0001c0001t0004g0339 |
4 | HG02723.hp2 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.902+2239G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375432 | |||||||
| chr6:89375472 | CGTGTGCA others(3): Show |
C | 65 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(62): Show |
69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.902+2189_902+2198d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375472 | |||||||
| chr6:89375557 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.902+2114G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375557 | |||||||
| chr6:89375726 | T | C | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.902+1945A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89375726 | |||||||
| chr6:89376175 | A | G | 7 | a0001c0001t0005g0017 a0001c0001t0005g0239 a0001c0001t0005g0240 others(4): Show |
8 | HG00280.hp1 HG00741.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.902+1496T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376175 | |||||||
| chr6:89376193 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.902+1478A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376193 | |||||||
| chr6:89376234 | C | T | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.902+1437G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376234 | |||||||
| chr6:89376290 | A | G | 254 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(251): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.902+1381T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376290 | |||||||
| chr6:89376300 | G | GGT | 14 | a0001c0001t0001g0015 a0001c0001t0001g0162 a0001c0001t0001g0193 others(11): Show |
15 | HG00741.hp2 HG01071.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.902+1369_902+1370d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | |||||||
| chr6:89376300 | GGT | G | 64 | a0001c0001t0001g0220 a0001c0001t0002g0003 a0001c0001t0002g0009 others(61): Show |
68 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(65): Show |
intron_variant | MODIFIER | c.902+1369_902+1370d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | |||||||
| chr6:89376300 | GGTGTGT | G | 12 | a0001c0001t0003g0060 a0001c0001t0003g0072 a0001c0001t0003g0073 others(9): Show |
12 | HG00741.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.902+1365_902+1370d others(8): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | |||||||
| chr6:89376300 | GGTGTGTG others(1): Show |
G | 156 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(153): Show |
168 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.902+1363_902+1370d others(10): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | |||||||
| chr6:89376300 | GGTGTGTG others(3): Show |
G | 6 | a0001c0001t0004g0290 a0001c0001t0015g0251 a0001c0001t0015g0252 others(3): Show |
6 | HG01081.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.902+1361_902+1370d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | |||||||
| chr6:89376300 | GGTGTGTG others(5): Show |
G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0175 a0001c0001t0001g0182 others(14): Show |
19 | HG00140.hp1 HG00423.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.902+1359_902+1370d others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376300 | |||||||
| chr6:89376302 | T | G | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.902+1369A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376302 | |||||||
| chr6:89376304 | T | G | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.902+1367A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376304 | |||||||
| chr6:89376308 | T | G | 4 | a0001c0001t0022g0249 a0001c0001t0022g0250 a0001c0001t0022g0311 others(1): Show |
4 | HG02451.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.902+1363A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376308 | |||||||
| chr6:89376310 | T | C | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.902+1361A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376310 | |||||||
| chr6:89376310 | T | G | 7 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(4): Show |
7 | HG02109.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.902+1361A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376310 | |||||||
| chr6:89376312 | T | C | 61 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(58): Show |
65 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(62): Show |
intron_variant | MODIFIER | c.902+1359A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376312 | |||||||
| chr6:89376312 | T | G | 5 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.902+1359A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376312 | |||||||
| chr6:89376314 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.902+1357A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376314 | |||||||
| chr6:89376705 | GCT | G | 16 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(13): Show |
16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.902+964_902+965del others(2): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376705 | |||||||
| chr6:89376736 | A | AT | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.902+934dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376736 | |||||||
| chr6:89376812 | G | A | 1 | a0001c0001t0008g0258 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.902+859C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376812 | |||||||
| chr6:89376895 | T | C | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.902+776A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376895 | |||||||
| chr6:89376935 | C | T | 65 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(62): Show |
69 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.902+736G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89376935 | |||||||
| chr6:89377098 | T | A | 1 | a0001c0001t0023g0247 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.902+573A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377098 | |||||||
| chr6:89377114 | G | A | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.902+557C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377114 | |||||||
| chr6:89377116 | G | A | 2 | a0001c0001t0016g0278 a0001c0001t0016g0280 |
2 | HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.902+555C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377116 | |||||||
| chr6:89377217 | G | T | 3 | a0001c0001t0004g0291 a0001c0001t0004g0294 a0001c0001t0004g0297 |
3 | HG00323.hp1 HG00735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.902+454C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377217 | |||||||
| chr6:89377252 | G | A | 1 | a0001c0001t0053g0226 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.902+419C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377252 | |||||||
| chr6:89377371 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.902+300G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377371 | |||||||
| chr6:89377447 | A | G | 1 | a0001c0001t0002g0138 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.902+224T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377447 | |||||||
| chr6:89377454 | G | C | 66 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(63): Show |
70 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.902+217C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377454 | |||||||
| chr6:89377495 | C | T | 1 | a0001c0001t0002g0155 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.902+176G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377495 | |||||||
| chr6:89377535 | T | C | 1 | a0001c0001t0002g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.902+136A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377535 | |||||||
| chr6:89377625 | G | A | 5 | a0001c0001t0020g0081 a0001c0001t0020g0083 a0001c0001t0020g0237 others(2): Show |
5 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.902+46C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 5/6 | chr6 | 89377625 | |||||||
| chr6:89377822 | T | A | 1 | a0001c0001t0052g0090 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.760-9A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89377822 | |||||||
| chr6:89377883 | T | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.760-70A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89377883 | |||||||
| chr6:89377931 | T | C | 67 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(64): Show |
72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.760-118A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89377931 | |||||||
| chr6:89377990 | A | G | 1 | a0001c0001t0011g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.760-177T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89377990 | |||||||
| chr6:89378058 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.760-245G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378058 | |||||||
| chr6:89378074 | C | T | 17 | a0001c0001t0001g0175 a0001c0001t0015g0251 a0001c0001t0015g0252 others(14): Show |
17 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.760-261G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378074 | |||||||
| chr6:89378092 | C | T | 248 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(245): Show |
264 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.760-279G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378092 | |||||||
| chr6:89378102 | G | A | 1 | a0001c0001t0009g0299 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.760-289C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378102 | |||||||
| chr6:89378116 | C | G | 2 | a0001c0001t0034g0071 a0001c0001t0035g0070 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.760-303G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378116 | |||||||
| chr6:89378121 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.760-308C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378121 | |||||||
| chr6:89378171 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0211 |
2 | HG01978.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.760-358C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378171 | |||||||
| chr6:89378205 | G | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.760-392C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378205 | |||||||
| chr6:89378240 | A | T | 132 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(129): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.760-427T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378240 | |||||||
| chr6:89378243 | G | A | 131 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(128): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.760-430C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378243 | |||||||
| chr6:89378264 | T | G | 4 | a0001c0001t0004g0261 a0001c0001t0004g0273 a0001c0001t0004g0274 others(1): Show |
4 | HG01081.hp2 HG03139.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-451A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378264 | |||||||
| chr6:89378274 | C | A | 66 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(63): Show |
70 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.760-461G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378274 | |||||||
| chr6:89378302 | C | CA | 43 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0271 others(40): Show |
45 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.760-490dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378302 | |||||||
| chr6:89378595 | C | T | 11 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0271 others(8): Show |
12 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.759+629G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378595 | |||||||
| chr6:89378752 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.759+472G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378752 | |||||||
| chr6:89378844 | A | G | 66 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(63): Show |
70 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.759+380T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378844 | |||||||
| chr6:89378856 | CAAGT | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(77): Show |
84 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(81): Show |
intron_variant | MODIFIER | c.759+364_759+367del others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378856 | |||||||
| chr6:89378936 | A | AT | 16 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(13): Show |
16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.759+287dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89378936 | |||||||
| chr6:89379145 | G | A | 1 | a0001c0001t0016g0280 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.759+79C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 4/6 | chr6 | 89379145 | |||||||
| chr6:89379352 | C | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.645-14G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379352 | |||||||
| chr6:89379456 | C | T | 1 | a0001c0001t0037g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.645-118G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379456 | |||||||
| chr6:89379589 | G | A | 1 | a0001c0001t0011g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.645-251C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379589 | |||||||
| chr6:89379632 | C | T | 2 | a0001c0001t0020g0237 a0001c0001t0041g0082 |
2 | HG01099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.645-294G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379632 | |||||||
| chr6:89379793 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.644+375C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379793 | |||||||
| chr6:89379850 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.644+318G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379850 | |||||||
| chr6:89379903 | T | C | 5 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+265A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379903 | |||||||
| chr6:89379958 | T | G | 140 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(137): Show |
149 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.644+210A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379958 | |||||||
| chr6:89379980 | G | A | 14 | a0001c0001t0003g0038 a0001c0001t0003g0143 a0001c0001t0003g0144 others(11): Show |
16 | HG00408.hp1 HG00735.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.644+188C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 3/6 | chr6 | 89379980 | |||||||
| chr6:89380506 | A | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.445-139T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380506 | |||||||
| chr6:89380539 | CAA | C | 65 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(62): Show |
69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.445-174_445-173del others(2): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380539 | |||||||
| chr6:89380562 | A | T | 65 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(62): Show |
69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.445-195T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380562 | |||||||
| chr6:89380645 | A | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
85 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(82): Show |
intron_variant | MODIFIER | c.445-278T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380645 | |||||||
| chr6:89380703 | T | C | 65 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(62): Show |
69 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(66): Show |
intron_variant | MODIFIER | c.445-336A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380703 | |||||||
| chr6:89380767 | C | T | 5 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-400G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380767 | |||||||
| chr6:89380912 | G | GA | 244 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(241): Show |
261 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.445-546dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380912 | |||||||
| chr6:89380912 | G | GAA | 9 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 others(6): Show |
9 | HG02258.hp2 HG02723.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-547_445-546dup others(2): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89380912 | |||||||
| chr6:89381075 | G | A | 1 | a0001c0001t0062g0286 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.445-708C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381075 | |||||||
| chr6:89381320 | A | G | 1 | a0001c0001t0012g0312 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.445-953T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381320 | |||||||
| chr6:89381371 | T | A | 3 | a0001c0001t0022g0249 a0001c0001t0022g0250 a0001c0001t0022g0311 |
3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.445-1004A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381371 | |||||||
| chr6:89381402 | G | C | 133 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(130): Show |
142 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.445-1035C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381402 | |||||||
| chr6:89381442 | A | C | 5 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-1075T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381442 | |||||||
| chr6:89381543 | T | C | 13 | a0001c0001t0006g0002 a0001c0001t0006g0084 a0001c0001t0006g0098 others(10): Show |
15 | HG00099.hp1 HG01109.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.445-1176A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381543 | |||||||
| chr6:89381677 | G | C | 1 | a0001c0001t0001g0199 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.445-1310C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381677 | |||||||
| chr6:89381728 | G | C | 52 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(49): Show |
54 | HG00438.hp2 HG00673.hp2 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.445-1361C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381728 | |||||||
| chr6:89381731 | C | T | 1 | a0001c0001t0005g0239 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.445-1364G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89381731 | |||||||
| chr6:89382017 | C | CA | 80 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(77): Show |
84 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(81): Show |
intron_variant | MODIFIER | c.445-1651dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382017 | |||||||
| chr6:89382079 | G | A | 7 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0326 others(4): Show |
8 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.445-1712C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382079 | |||||||
| chr6:89382284 | T | A | 1 | a0001c0001t0002g0127 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.445-1917A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382284 | |||||||
| chr6:89382329 | C | T | 1 | a0001c0001t0002g0112 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.445-1962G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382329 | |||||||
| chr6:89382400 | A | AAT | 12 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(9): Show |
12 | HG01106.hp1 HG01433.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.445-2035_445-2034d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATAT | 5 | a0001c0001t0003g0064 a0001c0001t0009g0289 a0001c0001t0009g0295 others(2): Show |
5 | HG00438.hp2 HG00741.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2037_445-2034d others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATAT | 93 | a0001c0001t0002g0160 a0001c0001t0003g0034 a0001c0001t0003g0039 others(90): Show |
98 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(95): Show |
intron_variant | MODIFIER | c.445-2039_445-2034d others(8): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(1): Show |
25 | a0001c0001t0002g0138 a0001c0001t0003g0038 a0001c0001t0003g0046 others(22): Show |
26 | HG00408.hp1 HG00423.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.445-2041_445-2034d others(10): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(3): Show |
9 | a0001c0001t0003g0008 a0001c0001t0003g0143 a0001c0001t0004g0291 others(6): Show |
10 | HG00323.hp1 HG00673.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.445-2043_445-2034d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(5): Show |
6 | a0001c0001t0004g0021 a0001c0001t0004g0339 a0001c0001t0016g0278 others(3): Show |
7 | HG02109.hp2 HG02723.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.445-2045_445-2034d others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(7): Show |
10 | a0001c0001t0003g0007 a0001c0001t0003g0042 a0001c0001t0003g0045 others(7): Show |
13 | HG00099.hp1 HG01123.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-2047_445-2034d others(16): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(9): Show |
5 | a0001c0001t0003g0043 a0001c0001t0010g0023 a0001c0001t0012g0270 others(2): Show |
5 | HG02040.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2049_445-2034d others(18): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(11): Show |
6 | a0001c0001t0002g0134 a0001c0001t0012g0312 a0001c0001t0012g0313 others(3): Show |
6 | HG01993.hp1 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-2051_445-2034d others(20): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(13): Show |
5 | a0001c0001t0002g0133 a0001c0001t0006g0098 a0001c0001t0016g0277 others(2): Show |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2053_445-2034d others(22): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(15): Show |
3 | a0001c0001t0002g0124 a0001c0001t0012g0285 a0001c0001t0050g0126 |
3 | HG01891.hp2 HG02040.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.445-2055_445-2034d others(24): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(17): Show |
7 | a0001c0001t0002g0111 a0001c0001t0002g0113 a0001c0001t0002g0119 others(4): Show |
7 | HG01261.hp2 HG02148.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(26): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(19): Show |
9 | a0001c0001t0002g0003 a0001c0001t0002g0106 a0001c0001t0002g0118 others(6): Show |
11 | HG00438.hp1 HG01952.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(28): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(21): Show |
6 | a0001c0001t0002g0012 a0001c0001t0002g0115 a0001c0001t0002g0149 others(3): Show |
7 | HG00621.hp2 HG02015.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(30): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(23): Show |
11 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0112 others(8): Show |
11 | HG01109.hp2 HG02080.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(32): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(25): Show |
6 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0006g0103 others(3): Show |
6 | HG02055.hp1 HG03139.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(34): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(27): Show |
3 | a0001c0001t0002g0140 a0001c0001t0002g0150 a0001c0001t0033g0030 |
3 | HG02132.hp1 NA18964.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.445-2034_445-2033i others(36): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(29): Show |
4 | a0001c0001t0002g0107 a0001c0001t0002g0127 a0001c0001t0002g0131 others(1): Show |
4 | NA18942.hp1 NA18943.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(38): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(31): Show |
5 | a0001c0001t0002g0117 a0001c0001t0002g0130 a0001c0001t0002g0148 others(2): Show |
5 | HG02451.hp1 NA18949.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(40): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(33): Show |
3 | a0001c0001t0002g0110 a0001c0001t0002g0116 a0001c0001t0002g0141 |
3 | HG02056.hp1 NA18965.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.445-2034_445-2033i others(42): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(35): Show |
4 | a0001c0001t0002g0009 a0001c0001t0002g0129 a0001c0001t0022g0249 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-2034_445-2033i others(44): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(37): Show |
1 | a0001c0001t0002g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.445-2034_445-2033i others(46): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | AATATATA others(39): Show |
1 | a0001c0001t0062g0286 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.445-2034_445-2033i others(48): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0135 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.445-2034_445-2033i others(27): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382400 | AAT | A | 5 | a0001c0001t0020g0081 a0001c0001t0020g0083 a0001c0001t0020g0237 others(2): Show |
5 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2035_445-2034d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382400 | |||||||
| chr6:89382468 | C | T | 1 | a0001c0001t0004g0306 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.445-2101G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382468 | |||||||
| chr6:89382498 | T | C | 254 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(251): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.445-2131A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382498 | |||||||
| chr6:89382602 | G | A | 3 | a0001c0001t0003g0034 a0001c0001t0003g0049 a0001c0001t0003g0169 |
3 | HG02155.hp1 NA18945.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.445-2235C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382602 | |||||||
| chr6:89382679 | G | A | 1 | a0001c0005t0036g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.445-2312C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382679 | |||||||
| chr6:89382685 | C | T | 1 | a0001c0001t0004g0288 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.445-2318G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382685 | |||||||
| chr6:89382884 | T | TA | 8 | a0001c0001t0011g0091 a0001c0002t0019g0330 a0001c0002t0019g0332 others(5): Show |
8 | HG02258.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.445-2518dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382884 | |||||||
| chr6:89382978 | C | T | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.445-2611G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382978 | |||||||
| chr6:89382980 | T | A | 16 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(13): Show |
16 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-2613A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89382980 | |||||||
| chr6:89383083 | T | C | 34 | a0001c0001t0004g0261 a0001c0001t0004g0273 a0001c0001t0004g0274 others(31): Show |
35 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.445-2716A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383083 | |||||||
| chr6:89383113 | A | G | 2 | a0001c0001t0009g0289 a0001c0001t0009g0295 |
2 | HG01516.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.445-2746T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383113 | |||||||
| chr6:89383257 | T | G | 1 | a0001c0001t0038g0068 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.445-2890A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383257 | |||||||
| chr6:89383403 | A | AG | 11 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 others(8): Show |
11 | HG02258.hp2 HG02723.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-3037dupC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383403 | |||||||
| chr6:89383417 | T | C | 1 | a0001c0001t0004g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.445-3050A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383417 | |||||||
| chr6:89383644 | G | A | 1 | a0001c0001t0009g0299 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.445-3277C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383644 | |||||||
| chr6:89383708 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.445-3341G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383708 | |||||||
| chr6:89383750 | C | T | 63 | a0001c0001t0001g0205 a0001c0001t0002g0003 a0001c0001t0002g0009 others(60): Show |
67 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(64): Show |
intron_variant | MODIFIER | c.445-3383G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383750 | |||||||
| chr6:89383787 | A | T | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.445-3420T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383787 | |||||||
| chr6:89383983 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.444+3312C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89383983 | |||||||
| chr6:89384100 | T | TA | 19 | a0001c0001t0001g0183 a0001c0001t0003g0066 a0001c0001t0007g0020 others(16): Show |
20 | HG01109.hp1 HG01433.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.444+3194dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384100 | |||||||
| chr6:89384310 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.444+2985G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384310 | |||||||
| chr6:89384341 | G | A | 7 | a0001c0001t0005g0017 a0001c0001t0005g0239 a0001c0001t0005g0240 others(4): Show |
8 | HG00280.hp1 HG00741.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+2954C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384341 | |||||||
| chr6:89384374 | T | C | 15 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+2921A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384374 | |||||||
| chr6:89384554 | C | T | 1 | a0001c0001t0008g0265 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.444+2741G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384554 | |||||||
| chr6:89384658 | T | C | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.444+2637A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384658 | |||||||
| chr6:89384687 | C | T | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.444+2608G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384687 | |||||||
| chr6:89384713 | G | A | 6 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(3): Show |
6 | HG02109.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.444+2582C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384713 | |||||||
| chr6:89384732 | G | A | 1 | a0001c0001t0020g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.444+2563C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384732 | |||||||
| chr6:89384771 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.444+2524C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384771 | |||||||
| chr6:89384813 | CA | C | 91 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0002g0109 others(88): Show |
97 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.444+2481delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384813 | |||||||
| chr6:89384813 | CAA | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(77): Show |
85 | HG00438.hp1 HG00621.hp2 HG01109.hp1 others(82): Show |
intron_variant | MODIFIER | c.444+2480_444+2481d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384813 | |||||||
| chr6:89384813 | CAAA | C | 12 | a0001c0001t0002g0135 a0001c0001t0002g0154 a0001c0001t0012g0315 others(9): Show |
12 | HG02109.hp2 HG02451.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.444+2479_444+2481d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89384813 | |||||||
| chr6:89385125 | T | C | 72 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(69): Show |
77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.444+2170A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385125 | |||||||
| chr6:89385404 | A | G | 1 | a0001c0001t0001g0013 | 2 | NA18948.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.444+1891T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385404 | |||||||
| chr6:89385638 | G | A | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.444+1657C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385638 | |||||||
| chr6:89385679 | G | A | 5 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(2): Show |
5 | HG02109.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+1616C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385679 | |||||||
| chr6:89385890 | G | A | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.444+1405C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385890 | |||||||
| chr6:89385903 | A | G | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.444+1392T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385903 | |||||||
| chr6:89385971 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.444+1324C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89385971 | |||||||
| chr6:89386026 | C | T | 15 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+1269G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386026 | |||||||
| chr6:89386063 | A | G | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.444+1232T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386063 | |||||||
| chr6:89386115 | T | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0189 a0001c0001t0029g0184 others(2): Show |
5 | HG00621.hp1 NA18964.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+1180A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386115 | |||||||
| chr6:89386121 | G | A | 1 | a0001c0001t0006g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.444+1174C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386121 | |||||||
| chr6:89386132 | A | C | 1 | a0001c0001t0009g0307 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.444+1163T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386132 | |||||||
| chr6:89386202 | T | A | 15 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+1093A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386202 | |||||||
| chr6:89386224 | C | T | 1 | a0001c0001t0005g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.444+1071G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386224 | |||||||
| chr6:89386237 | T | G | 15 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+1058A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386237 | |||||||
| chr6:89386254 | A | G | 21 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0271 others(18): Show |
23 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.444+1041T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386254 | |||||||
| chr6:89386351 | C | T | 1 | a0001c0001t0045g0077 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.444+944G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386351 | |||||||
| chr6:89386794 | G | C | 1 | a0001c0001t0003g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.444+501C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386794 | |||||||
| chr6:89386814 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.444+481G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386814 | |||||||
| chr6:89386964 | T | C | 15 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+331A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89386964 | |||||||
| chr6:89387085 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.444+210C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 2/6 | chr6 | 89387085 | |||||||
| chr6:89387707 | A | G | 6 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-117T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89387707 | |||||||
| chr6:89387824 | C | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149-234G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89387824 | |||||||
| chr6:89387877 | A | G | 3 | a0001c0001t0015g0252 a0001c0001t0015g0253 a0001c0001t0015g0254 |
3 | HG02451.hp2 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-287T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89387877 | |||||||
| chr6:89388149 | G | A | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.149-559C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388149 | |||||||
| chr6:89388440 | T | G | 2 | a0001c0001t0011g0089 a0001c0001t0011g0093 |
2 | HG00738.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.149-850A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388440 | |||||||
| chr6:89388510 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.149-920G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388510 | |||||||
| chr6:89388593 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.149-1003G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388593 | |||||||
| chr6:89388666 | G | C | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-1076C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388666 | |||||||
| chr6:89388893 | C | A | 1 | a0001c0001t0009g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.149-1303G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89388893 | |||||||
| chr6:89389026 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.149-1436G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389026 | |||||||
| chr6:89389104 | AGGTCTGT others(12): Show |
A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0232 |
2 | NA18945.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.149-1533_149-1515d others(21): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389104 | |||||||
| chr6:89389326 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.149-1736G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389326 | |||||||
| chr6:89389395 | A | T | 71 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(68): Show |
76 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.149-1805T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389395 | |||||||
| chr6:89389487 | C | T | 6 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-1897G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389487 | |||||||
| chr6:89389488 | G | A | 9 | a0001c0001t0014g0006 a0001c0001t0014g0035 a0001c0001t0014g0036 others(6): Show |
10 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-1898C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389488 | |||||||
| chr6:89389496 | C | T | 16 | a0001c0001t0004g0281 a0001c0001t0004g0283 a0001c0001t0004g0288 others(13): Show |
16 | HG00323.hp1 HG00423.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.149-1906G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389496 | |||||||
| chr6:89389555 | C | CA | 92 | a0001c0001t0001g0185 a0001c0001t0001g0220 a0001c0001t0001g0228 others(89): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.149-1966dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389555 | |||||||
| chr6:89389555 | C | CAA | 11 | a0001c0001t0001g0199 a0001c0001t0002g0120 a0001c0001t0002g0158 others(8): Show |
11 | HG00438.hp1 HG00741.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.149-1967_149-1966d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389555 | |||||||
| chr6:89389745 | T | C | 2 | a0001c0001t0003g0072 a0001c0001t0003g0073 |
2 | NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.149-2155A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89389745 | |||||||
| chr6:89390180 | G | GA | 18 | a0001c0001t0001g0215 a0001c0001t0001g0232 a0001c0001t0002g0137 others(15): Show |
18 | HG01069.hp1 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.149-2591dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390180 | |||||||
| chr6:89390195 | A | G | 1 | a0001c0001t0006g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.149-2605T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390195 | |||||||
| chr6:89390577 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.149-2987A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390577 | |||||||
| chr6:89390796 | G | A | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-3206C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390796 | |||||||
| chr6:89390867 | C | T | 1 | a0001c0001t0055g0296 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.149-3277G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390867 | |||||||
| chr6:89390924 | A | G | 20 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0271 others(17): Show |
22 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.149-3334T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89390924 | |||||||
| chr6:89391168 | T | G | 1 | a0001c0001t0060g0309 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.149-3578A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391168 | |||||||
| chr6:89391293 | A | G | 249 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(246): Show |
265 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.149-3703T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391293 | |||||||
| chr6:89391294 | A | G | 1 | a0001c0001t0003g0046 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.149-3704T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391294 | |||||||
| chr6:89391384 | C | CA | 79 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(76): Show |
83 | HG00438.hp1 HG00621.hp2 HG01099.hp2 others(80): Show |
intron_variant | MODIFIER | c.149-3795dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391384 | |||||||
| chr6:89391415 | T | C | 73 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(70): Show |
78 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.149-3825A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391415 | |||||||
| chr6:89391453 | C | T | 2 | a0001c0001t0003g0058 a0001c0001t0003g0065 |
2 | NA18981.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.149-3863G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391453 | |||||||
| chr6:89391472 | A | G | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.149-3882T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391472 | |||||||
| chr6:89391683 | T | C | 3 | a0001c0001t0022g0249 a0001c0001t0022g0250 a0001c0001t0022g0311 |
3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.149-4093A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391683 | |||||||
| chr6:89391798 | A | G | 1 | a0001c0001t0011g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.149-4208T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391798 | |||||||
| chr6:89391948 | C | A | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.149-4358G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391948 | |||||||
| chr6:89391956 | C | CA | 26 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0001g0200 others(23): Show |
28 | HG00280.hp1 HG00408.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.149-4367dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | |||||||
| chr6:89391956 | C | CAA | 43 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0316 others(40): Show |
47 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.149-4368_149-4367d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | |||||||
| chr6:89391956 | C | CAAA | 41 | a0001c0001t0004g0261 a0001c0001t0004g0273 a0001c0001t0004g0281 others(38): Show |
43 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.149-4369_149-4367d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | |||||||
| chr6:89391956 | C | CAAAA | 12 | a0001c0001t0004g0274 a0001c0001t0004g0282 a0001c0001t0004g0308 others(9): Show |
13 | HG00733.hp2 HG01081.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.149-4370_149-4367d others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | |||||||
| chr6:89391956 | CA | C | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0229 others(3): Show |
6 | HG01169.hp2 HG01258.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-4367delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391956 | |||||||
| chr6:89391969 | A | AAAAAG | 72 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0106 others(69): Show |
75 | HG00438.hp1 HG01261.hp2 HG01891.hp2 others(72): Show |
intron_variant | MODIFIER | c.149-4380_149-4379i others(7): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89391969 | |||||||
| chr6:89392047 | T | C | 4 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0166 others(1): Show |
4 | NA18944.hp1 NA18947.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-4457A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392047 | |||||||
| chr6:89392151 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.149-4561T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392151 | |||||||
| chr6:89392231 | T | C | 7 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(4): Show |
7 | HG01515.hp2 HG01934.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-4641A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392231 | |||||||
| chr6:89392255 | C | T | 1 | a0001c0001t0003g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.149-4665G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392255 | |||||||
| chr6:89392346 | G | A | 3 | a0001c0001t0002g0121 a0001c0001t0002g0137 a0001c0001t0002g0152 |
3 | NA18974.hp2 NA18981.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.149-4756C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392346 | |||||||
| chr6:89392372 | T | C | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.149-4782A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392372 | |||||||
| chr6:89392387 | G | A | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-4797C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392387 | |||||||
| chr6:89392444 | C | G | 1 | a0001c0001t0001g0189 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.149-4854G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392444 | |||||||
| chr6:89392445 | A | G | 3 | a0001c0001t0011g0091 a0001c0001t0011g0092 a0001c0001t0011g0094 |
3 | HG02559.hp2 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.149-4855T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392445 | |||||||
| chr6:89392479 | C | CA | 180 | a0001c0001t0002g0156 a0001c0001t0003g0007 a0001c0001t0003g0008 others(177): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.149-4890_149-4889i others(3): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392479 | |||||||
| chr6:89392479 | C | CAA | 66 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(63): Show |
70 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(67): Show |
intron_variant | MODIFIER | c.149-4890_149-4889i others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392479 | |||||||
| chr6:89392480 | G | A | 254 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(251): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.149-4890C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392480 | |||||||
| chr6:89392756 | G | A | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.149-5166C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392756 | |||||||
| chr6:89392782 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.149-5192A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392782 | |||||||
| chr6:89392797 | A | T | 1 | a0001c0001t0010g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.149-5207T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392797 | |||||||
| chr6:89392904 | G | A | 77 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(74): Show |
81 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(78): Show |
intron_variant | MODIFIER | c.149-5314C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89392904 | |||||||
| chr6:89393032 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.149-5442T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393032 | |||||||
| chr6:89393095 | C | T | 1 | a0001c0001t0060g0309 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.149-5505G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393095 | |||||||
| chr6:89393151 | T | G | 255 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(252): Show |
272 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.149-5561A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393151 | |||||||
| chr6:89393191 | T | C | 1 | a0001c0001t0007g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.149-5601A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393191 | |||||||
| chr6:89393285 | C | T | 1 | a0001c0001t0004g0300 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.149-5695G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393285 | |||||||
| chr6:89393467 | T | A | 2 | a0001c0001t0003g0057 a0001c0001t0003g0060 |
2 | NA18946.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.149-5877A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393467 | |||||||
| chr6:89393636 | G | C | 15 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(12): Show |
15 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.149-6046C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89393636 | |||||||
| chr6:89394047 | G | T | 11 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(8): Show |
11 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.149-6457C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394047 | |||||||
| chr6:89394085 | T | G | 3 | a0001c0001t0022g0249 a0001c0001t0022g0250 a0001c0001t0022g0311 |
3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.149-6495A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394085 | |||||||
| chr6:89394164 | A | T | 2 | a0001c0001t0005g0011 a0001c0001t0027g0085 |
3 | HG00738.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.149-6574T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394164 | |||||||
| chr6:89394167 | G | C | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-6577C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394167 | |||||||
| chr6:89394231 | T | TA | 11 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(8): Show |
11 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.149-6642dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394231 | |||||||
| chr6:89394311 | A | T | 5 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-6721T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394311 | |||||||
| chr6:89394359 | G | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149-6769C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394359 | |||||||
| chr6:89394398 | A | G | 254 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(251): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.149-6808T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394398 | |||||||
| chr6:89394676 | C | T | 65 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.149-7086G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89394676 | |||||||
| chr6:89395368 | T | C | 2 | a0001c0001t0003g0045 a0001c0001t0009g0299 |
2 | HG04228.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.149-7778A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395368 | |||||||
| chr6:89395378 | C | T | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.149-7788G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395378 | |||||||
| chr6:89395553 | T | C | 12 | a0001c0001t0005g0011 a0001c0001t0005g0017 a0001c0001t0005g0087 others(9): Show |
14 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.149-7963A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395553 | |||||||
| chr6:89395620 | G | C | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.149-8030C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395620 | |||||||
| chr6:89395762 | T | C | 10 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-8172A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395762 | |||||||
| chr6:89395969 | C | CA | 253 | a0001c0001t0001g0222 a0001c0001t0002g0003 a0001c0001t0002g0009 others(250): Show |
270 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.149-8380dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89395969 | |||||||
| chr6:89396404 | G | GAAAAC | 254 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(251): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.149-8815_149-8814i others(7): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396404 | |||||||
| chr6:89396421 | T | TTTTA | 74 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(71): Show |
78 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(75): Show |
intron_variant | MODIFIER | c.149-8835_149-8832d others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396421 | |||||||
| chr6:89396616 | G | A | 7 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(4): Show |
7 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-9026C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396616 | |||||||
| chr6:89396643 | T | G | 1 | a0001c0001t0019g0275 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.149-9053A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396643 | |||||||
| chr6:89396649 | G | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149-9059C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396649 | |||||||
| chr6:89396728 | A | AT | 39 | a0001c0001t0001g0172 a0001c0001t0001g0175 a0001c0001t0001g0177 others(36): Show |
40 | HG00423.hp2 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.149-9139dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | |||||||
| chr6:89396728 | AT | A | 59 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0186 others(56): Show |
65 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.149-9139delA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | |||||||
| chr6:89396728 | ATT | A | 11 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0111 others(8): Show |
11 | HG00438.hp1 HG01952.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.149-9140_149-9139d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | |||||||
| chr6:89396728 | ATTT | A | 50 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(47): Show |
54 | HG00621.hp2 HG01261.hp2 HG01891.hp2 others(51): Show |
intron_variant | MODIFIER | c.149-9141_149-9139d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | |||||||
| chr6:89396728 | ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0145 others(3): Show |
6 | HG00438.hp2 HG02055.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-9146_149-9139d others(10): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | |||||||
| chr6:89396728 | ATTTTTTT others(2): Show |
A | 56 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(53): Show |
60 | HG00408.hp1 HG00673.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.149-9147_149-9139d others(11): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | |||||||
| chr6:89396728 | ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0003g0045 a0001c0001t0017g0167 a0001c0001t0017g0170 |
3 | NA18951.hp2 NA18959.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.149-9148_149-9139d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396728 | |||||||
| chr6:89396737 | T | A | 1 | a0001c0001t0003g0056 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.149-9147A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396737 | |||||||
| chr6:89396744 | T | A | 1 | a0001c0001t0003g0168 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.149-9154A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396744 | |||||||
| chr6:89396945 | C | T | 65 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.149-9355G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89396945 | |||||||
| chr6:89397000 | C | T | 1 | a0001c0001t0024g0263 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.149-9410G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397000 | |||||||
| chr6:89397001 | G | A | 67 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(64): Show |
71 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.149-9411C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397001 | |||||||
| chr6:89397228 | A | AG | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.149-9639dupC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397228 | |||||||
| chr6:89397521 | G | A | 10 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-9931C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397521 | |||||||
| chr6:89397603 | C | CA | 19 | a0001c0001t0001g0232 a0001c0001t0002g0138 a0001c0001t0002g0153 others(16): Show |
19 | HG00438.hp2 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.149-10014dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397603 | |||||||
| chr6:89397604 | AAAAAAAA others(3): Show |
A | 5 | a0001c0001t0005g0011 a0001c0001t0005g0087 a0001c0001t0005g0088 others(2): Show |
6 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-10024_149-1001 others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397604 | |||||||
| chr6:89397614 | C | A | 6 | a0001c0001t0001g0185 a0001c0002t0019g0332 a0001c0002t0021g0331 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-10024G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397614 | |||||||
| chr6:89397614 | C | CA | 5 | a0001c0001t0002g0111 a0001c0001t0002g0132 a0001c0001t0004g0322 others(2): Show |
5 | HG01261.hp2 HG02258.hp1 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-10025dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397614 | |||||||
| chr6:89397623 | ACAAAAAA others(3): Show |
A | 6 | a0001c0001t0005g0017 a0001c0001t0005g0239 a0001c0001t0005g0240 others(3): Show |
7 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-10043_149-1003 others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397623 | |||||||
| chr6:89397633 | C | A | 241 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(238): Show |
256 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.149-10043G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397633 | |||||||
| chr6:89397674 | C | T | 3 | a0001c0001t0022g0249 a0001c0001t0022g0250 a0001c0001t0022g0311 |
3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.149-10084G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397674 | |||||||
| chr6:89397818 | A | T | 1 | a0001c0001t0002g0122 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.149-10228T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397818 | |||||||
| chr6:89397885 | A | T | 1 | a0001c0001t0008g0256 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.149-10295T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89397885 | |||||||
| chr6:89398207 | G | C | 4 | a0001c0001t0003g0061 a0001c0001t0003g0063 a0001c0001t0003g0064 others(1): Show |
4 | HG00438.hp2 NA18953.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.149-10617C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398207 | |||||||
| chr6:89398221 | A | G | 17 | a0001c0001t0005g0011 a0001c0001t0005g0017 a0001c0001t0005g0087 others(14): Show |
19 | HG00280.hp1 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.149-10631T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398221 | |||||||
| chr6:89398226 | G | A | 65 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.149-10636C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398226 | |||||||
| chr6:89398298 | C | T | 1 | a0001c0001t0011g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.149-10708G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398298 | |||||||
| chr6:89398329 | T | C | 6 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-10739A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398329 | |||||||
| chr6:89398552 | G | C | 1 | a0001c0001t0011g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.149-10962C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398552 | |||||||
| chr6:89398570 | C | T | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.149-10980G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398570 | |||||||
| chr6:89398859 | C | G | 67 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(64): Show |
71 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.149-11269G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89398859 | |||||||
| chr6:89399103 | G | A | 10 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.149-11513C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399103 | |||||||
| chr6:89399174 | T | C | 1 | a0001c0001t0004g0283 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.149-11584A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399174 | |||||||
| chr6:89399192 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0139 |
2 | NA19005.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.149-11602G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399192 | |||||||
| chr6:89399349 | A | G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | NA19054.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.149-11759T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399349 | |||||||
| chr6:89399567 | T | C | 1 | a0001c0001t0028g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.149-11977A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399567 | |||||||
| chr6:89399622 | T | A | 2 | a0001c0001t0026g0099 a0001c0001t0026g0100 |
2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.149-12032A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399622 | |||||||
| chr6:89399622 | T | G | 2 | a0001c0001t0034g0071 a0001c0001t0035g0070 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.149-12032A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399622 | |||||||
| chr6:89399651 | G | A | 1 | a0001c0001t0063g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.149-12061C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399651 | |||||||
| chr6:89399655 | C | T | 71 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(68): Show |
76 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.149-12065G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399655 | |||||||
| chr6:89399767 | A | AT | 184 | a0001c0001t0001g0176 a0001c0001t0001g0189 a0001c0001t0002g0003 others(181): Show |
195 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.148+12078dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399767 | |||||||
| chr6:89399767 | A | ATT | 50 | a0001c0001t0001g0175 a0001c0001t0002g0121 a0001c0001t0002g0150 others(47): Show |
54 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.148+12077_148+1207 others(6): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399767 | |||||||
| chr6:89399767 | A | ATTT | 11 | a0001c0001t0007g0329 a0001c0001t0014g0006 a0001c0001t0014g0035 others(8): Show |
12 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.148+12076_148+1207 others(7): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399767 | |||||||
| chr6:89399767 | A | ATTTT | 10 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0271 others(7): Show |
11 | HG01109.hp1 HG02257.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+12075_148+1207 others(8): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399767 | |||||||
| chr6:89399835 | C | T | 1 | a0001c0001t0003g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.148+12011G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399835 | |||||||
| chr6:89399858 | C | T | 1 | a0001c0001t0064g0343 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.148+11988G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399858 | |||||||
| chr6:89399977 | G | A | 2 | a0001c0001t0003g0145 a0001c0001t0003g0147 |
2 | HG02055.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.148+11869C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89399977 | |||||||
| chr6:89400129 | C | T | 1 | a0001c0001t0054g0244 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.148+11717G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400129 | |||||||
| chr6:89400409 | A | T | 340 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(337): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.148+11437T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400409 | |||||||
| chr6:89400595 | T | TA | 156 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(153): Show |
165 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.148+11250dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400595 | |||||||
| chr6:89400698 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0222 |
3 | NA19006.hp1 NA19065.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.148+11148C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400698 | |||||||
| chr6:89400749 | C | T | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.148+11097G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400749 | |||||||
| chr6:89400765 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.148+11081G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400765 | |||||||
| chr6:89400948 | T | C | 1 | a0001c0001t0030g0304 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.148+10898A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89400948 | |||||||
| chr6:89401059 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.148+10787G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401059 | |||||||
| chr6:89401246 | G | A | 1 | a0001c0001t0045g0077 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.148+10600C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401246 | |||||||
| chr6:89401261 | TA | T | 62 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(59): Show |
66 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(63): Show |
intron_variant | MODIFIER | c.148+10584delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401261 | |||||||
| chr6:89401262 | A | AT | 71 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(68): Show |
75 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.148+10583dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401262 | |||||||
| chr6:89401262 | A | T | 10 | a0001c0001t0002g0111 a0001c0001t0016g0276 a0001c0001t0016g0277 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+10584T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401262 | |||||||
| chr6:89401356 | C | G | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.148+10490G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401356 | |||||||
| chr6:89401452 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.148+10394G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401452 | |||||||
| chr6:89401461 | G | A | 1 | a0001c0001t0030g0304 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.148+10385C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401461 | |||||||
| chr6:89401464 | C | T | 12 | a0001c0001t0005g0017 a0001c0001t0005g0239 a0001c0001t0005g0240 others(9): Show |
13 | HG00280.hp1 HG00741.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.148+10382G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401464 | |||||||
| chr6:89401628 | TTGTTCCC | T | 10 | a0001c0001t0016g0276 a0001c0001t0016g0277 a0001c0001t0016g0278 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+10211_148+1021 others(11): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401628 | |||||||
| chr6:89401681 | A | C | 4 | a0001c0001t0014g0006 a0001c0001t0014g0035 a0001c0001t0014g0036 others(1): Show |
5 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+10165T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401681 | |||||||
| chr6:89401760 | A | G | 3 | a0001c0001t0006g0098 a0001c0001t0006g0101 a0001c0001t0037g0097 |
3 | HG01109.hp2 HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.148+10086T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89401760 | |||||||
| chr6:89402038 | A | AT | 27 | a0001c0001t0001g0067 a0001c0001t0001g0075 a0001c0001t0001g0174 others(24): Show |
30 | HG00621.hp1 HG00735.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.148+9807dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATT | 12 | a0001c0001t0005g0011 a0001c0001t0005g0017 a0001c0001t0005g0087 others(9): Show |
14 | HG00280.hp1 HG00738.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.148+9806_148+9807d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(1): Show |
18 | a0001c0001t0006g0002 a0001c0001t0006g0101 a0001c0001t0006g0102 others(15): Show |
20 | HG00099.hp1 HG01109.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.148+9800_148+9807d others(10): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(2): Show |
22 | a0001c0001t0004g0305 a0001c0001t0004g0308 a0001c0001t0006g0084 others(19): Show |
22 | HG00733.hp2 HG00738.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.148+9799_148+9807d others(11): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(3): Show |
23 | a0001c0001t0004g0274 a0001c0001t0004g0282 a0001c0001t0004g0283 others(20): Show |
23 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.148+9798_148+9807d others(12): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(4): Show |
54 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(51): Show |
61 | HG00423.hp1 HG00621.hp2 HG01261.hp2 others(58): Show |
intron_variant | MODIFIER | c.148+9797_148+9807d others(13): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(5): Show |
24 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0115 others(21): Show |
24 | HG00323.hp1 HG00438.hp1 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.148+9796_148+9807d others(14): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(10): Show |
7 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0272 others(4): Show |
8 | HG02257.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+9807_148+9808i others(19): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0007g0326 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.148+9807_148+9808i others(20): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(6): Show |
29 | a0001c0001t0002g0110 a0001c0001t0002g0111 a0001c0001t0002g0154 others(26): Show |
29 | HG00408.hp1 HG00438.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.148+9795_148+9807d others(15): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(7): Show |
28 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(25): Show |
30 | HG00673.hp2 HG01255.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.148+9794_148+9807d others(16): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(8): Show |
10 | a0001c0001t0003g0046 a0001c0001t0003g0066 a0001c0001t0003g0072 others(7): Show |
10 | HG01069.hp2 HG02523.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+9793_148+9807d others(17): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(9): Show |
3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0035g0070 |
3 | HG01071.hp2 HG01934.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.148+9792_148+9807d others(18): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402038 | A | ATTTTTTT others(11): Show |
3 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0109 |
3 | HG02080.hp1 NA18943.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.148+9790_148+9807d others(20): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402038 | |||||||
| chr6:89402046 | T | TTTTTCTT others(10): Show |
1 | a0001c0001t0007g0271 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.148+9799_148+9800i others(19): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402046 | |||||||
| chr6:89402127 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.148+9719T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402127 | |||||||
| chr6:89402237 | G | A | 65 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(62): Show |
69 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.148+9609C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402237 | |||||||
| chr6:89402289 | G | A | 2 | a0001c0001t0002g0139 a0001c0002t0040g0031 |
2 | NA19056.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.148+9557C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402289 | |||||||
| chr6:89402561 | G | C | 6 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+9285C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402561 | |||||||
| chr6:89402639 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.148+9207C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402639 | |||||||
| chr6:89402729 | A | T | 1 | a0001c0001t0010g0023 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.148+9117T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402729 | |||||||
| chr6:89402809 | T | C | 1 | a0001c0002t0021g0335 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.148+9037A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402809 | |||||||
| chr6:89402910 | T | G | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.148+8936A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89402910 | |||||||
| chr6:89403164 | G | A | 5 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+8682C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403164 | |||||||
| chr6:89403167 | C | A | 6 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+8679G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403167 | |||||||
| chr6:89403170 | G | A | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.148+8676C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403170 | |||||||
| chr6:89403180 | G | A | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0049g0225 others(1): Show |
4 | HG01943.hp2 HG02148.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.148+8666C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403180 | |||||||
| chr6:89403231 | G | A | 1 | a0001c0001t0012g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.148+8615C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403231 | |||||||
| chr6:89403242 | G | A | 1 | a0001c0001t0004g0288 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.148+8604C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403242 | |||||||
| chr6:89403264 | T | C | 1 | a0001c0001t0004g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.148+8582A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403264 | |||||||
| chr6:89403306 | A | G | 77 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(74): Show |
81 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.148+8540T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403306 | |||||||
| chr6:89403308 | G | A | 65 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(62): Show |
70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.148+8538C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403308 | |||||||
| chr6:89403311 | G | A | 75 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0034 others(72): Show |
79 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.148+8535C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403311 | |||||||
| chr6:89403317 | C | T | 1 | a0001c0001t0037g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.148+8529G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403317 | |||||||
| chr6:89403362 | G | A | 4 | a0001c0001t0014g0006 a0001c0001t0014g0035 a0001c0001t0014g0036 others(1): Show |
5 | HG02486.hp2 HG02559.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+8484C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403362 | |||||||
| chr6:89403423 | C | T | 2 | a0001c0001t0003g0050 a0001c0001t0003g0051 |
2 | HG01934.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.148+8423G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403423 | |||||||
| chr6:89403453 | A | C | 1 | a0001c0001t0004g0290 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.148+8393T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403453 | |||||||
| chr6:89403538 | C | T | 247 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(244): Show |
263 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.148+8308G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403538 | |||||||
| chr6:89403556 | T | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(78): Show |
86 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+8290A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403556 | |||||||
| chr6:89403627 | CT | C | 95 | a0001c0001t0002g0106 a0001c0001t0003g0007 a0001c0001t0003g0008 others(92): Show |
101 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.148+8218delA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403627 | |||||||
| chr6:89403627 | CTT | C | 85 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(82): Show |
91 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.148+8217_148+8218d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403627 | |||||||
| chr6:89403627 | CTTT | C | 64 | a0001c0001t0002g0141 a0001c0001t0004g0019 a0001c0001t0004g0261 others(61): Show |
68 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.148+8216_148+8218d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403627 | |||||||
| chr6:89403700 | T | C | 7 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(4): Show |
7 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+8146A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403700 | |||||||
| chr6:89403795 | C | G | 6 | a0001c0001t0005g0017 a0001c0001t0005g0239 a0001c0001t0005g0240 others(3): Show |
7 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+8051G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403795 | |||||||
| chr6:89403854 | C | T | 1 | a0001c0001t0025g0340 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.148+7992G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89403854 | |||||||
| chr6:89404082 | T | A | 1 | a0001c0001t0010g0023 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.148+7764A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404082 | |||||||
| chr6:89404290 | A | C | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.148+7556T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404290 | |||||||
| chr6:89404311 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.148+7535A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404311 | |||||||
| chr6:89404409 | C | T | 6 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+7437G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404409 | |||||||
| chr6:89404422 | G | T | 72 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(69): Show |
77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.148+7424C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404422 | |||||||
| chr6:89404650 | G | A | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+7196C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404650 | |||||||
| chr6:89404710 | C | A | 1 | a0001c0004t0039g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.148+7136G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404710 | |||||||
| chr6:89404897 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(79): Show |
88 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.148+6949G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404897 | |||||||
| chr6:89404904 | A | T | 1 | a0001c0001t0010g0023 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.148+6942T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404904 | |||||||
| chr6:89404941 | T | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0162 a0001c0001t0001g0228 others(1): Show |
4 | HG00140.hp2 HG01257.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+6905A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404941 | |||||||
| chr6:89404955 | G | C | 40 | a0001c0001t0003g0038 a0001c0001t0003g0143 a0001c0001t0003g0144 others(37): Show |
44 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.148+6891C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404955 | |||||||
| chr6:89404959 | T | C | 32 | a0001c0001t0003g0038 a0001c0001t0003g0143 a0001c0001t0003g0144 others(29): Show |
36 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.148+6887A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89404959 | |||||||
| chr6:89405022 | A | G | 5 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(2): Show |
5 | NA18968.hp1 NA18979.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+6824T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405022 | |||||||
| chr6:89405083 | G | C | 44 | a0001c0001t0004g0019 a0001c0001t0004g0021 a0001c0001t0004g0261 others(41): Show |
47 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.148+6763C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405083 | |||||||
| chr6:89405151 | T | C | 1 | a0001c0001t0011g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.148+6695A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405151 | |||||||
| chr6:89405166 | C | A | 7 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0326 others(4): Show |
8 | HG01109.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+6680G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405166 | |||||||
| chr6:89405167 | G | A | 2 | a0001c0001t0031g0266 a0001c0001t0031g0267 |
2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.148+6679C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405167 | |||||||
| chr6:89405169 | T | A | 3 | a0001c0001t0022g0249 a0001c0001t0022g0250 a0001c0001t0022g0311 |
3 | HG02451.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.148+6677A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405169 | |||||||
| chr6:89405224 | T | G | 1 | a0001c0001t0059g0320 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.148+6622A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405224 | |||||||
| chr6:89405328 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.148+6518A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405328 | |||||||
| chr6:89405353 | C | CA | 120 | a0001c0001t0001g0172 a0001c0001t0001g0231 a0001c0001t0001g0232 others(117): Show |
126 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.148+6492dupT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405353 | |||||||
| chr6:89405353 | C | CAA | 37 | a0001c0001t0002g0154 a0001c0001t0003g0038 a0001c0001t0003g0046 others(34): Show |
40 | HG00280.hp1 HG00408.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.148+6491_148+6492d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405353 | |||||||
| chr6:89405353 | C | CAAA | 9 | a0001c0001t0005g0017 a0001c0001t0005g0241 a0001c0001t0005g0242 others(6): Show |
10 | HG01169.hp1 HG01358.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+6490_148+6492d others(5): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405353 | |||||||
| chr6:89405374 | A | G | 8 | a0001c0001t0011g0089 a0001c0001t0011g0091 a0001c0001t0011g0092 others(5): Show |
8 | HG00738.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.148+6472T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405374 | |||||||
| chr6:89405591 | G | A | 18 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0326 others(15): Show |
20 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.148+6255C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405591 | |||||||
| chr6:89405752 | C | T | 80 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(77): Show |
86 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.148+6094G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405752 | |||||||
| chr6:89405842 | G | A | 2 | a0001c0001t0004g0322 a0001c0001t0004g0323 |
2 | HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.148+6004C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405842 | |||||||
| chr6:89405972 | G | C | 2 | a0001c0001t0008g0264 a0001c0001t0008g0265 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.148+5874C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89405972 | |||||||
| chr6:89406071 | G | A | 2 | a0001c0001t0034g0071 a0001c0001t0035g0070 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.148+5775C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406071 | |||||||
| chr6:89406100 | CAA | C | 15 | a0001c0001t0003g0007 a0001c0001t0003g0039 a0001c0001t0003g0040 others(12): Show |
16 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.148+5744_148+5745d others(4): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406100 | |||||||
| chr6:89406174 | TA | T | 6 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+5671delT | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406174 | |||||||
| chr6:89406180 | T | A | 6 | a0001c0001t0002g0012 a0001c0001t0002g0155 a0001c0001t0002g0156 others(3): Show |
7 | HG00438.hp1 NA18967.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+5666A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406180 | |||||||
| chr6:89406189 | T | C | 28 | a0001c0001t0003g0038 a0001c0001t0005g0011 a0001c0001t0005g0017 others(25): Show |
32 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.148+5657A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406189 | |||||||
| chr6:89406199 | G | T | 7 | a0001c0002t0019g0330 a0001c0002t0019g0332 a0001c0002t0021g0331 others(4): Show |
7 | HG02258.hp2 HG02723.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+5647C>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406199 | |||||||
| chr6:89406204 | G | C | 19 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0326 others(16): Show |
21 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.148+5642C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406204 | |||||||
| chr6:89406267 | A | G | 42 | a0001c0001t0003g0038 a0001c0001t0005g0011 a0001c0001t0005g0017 others(39): Show |
46 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.148+5579T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406267 | |||||||
| chr6:89406383 | G | A | 247 | a0001c0001t0001g0162 a0001c0001t0002g0003 a0001c0001t0002g0009 others(244): Show |
263 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.148+5463C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406383 | |||||||
| chr6:89406425 | C | T | 79 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0012 others(76): Show |
85 | HG00099.hp1 HG00438.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.148+5421G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406425 | |||||||
| chr6:89406455 | C | A | 1 | a0001c0001t0003g0066 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.148+5391G>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406455 | |||||||
| chr6:89406536 | A | G | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+5310T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406536 | |||||||
| chr6:89406673 | C | T | 3 | a0001c0001t0004g0261 a0001c0001t0004g0273 a0001c0001t0004g0274 |
3 | HG01081.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.148+5173G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406673 | |||||||
| chr6:89406683 | G | A | 8 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(5): Show |
8 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.148+5163C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406683 | |||||||
| chr6:89406858 | TG | T | 7 | a0001c0001t0012g0270 a0001c0001t0012g0284 a0001c0001t0012g0285 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+4987delC | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406858 | |||||||
| chr6:89406911 | C | G | 33 | a0001c0001t0003g0038 a0001c0001t0005g0011 a0001c0001t0005g0017 others(30): Show |
37 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.148+4935G>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89406911 | |||||||
| chr6:89407301 | T | A | 56 | a0001c0001t0001g0162 a0001c0001t0003g0007 a0001c0001t0003g0008 others(53): Show |
58 | HG00438.hp2 HG00673.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.148+4545A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407301 | |||||||
| chr6:89407308 | T | A | 1 | a0001c0001t0004g0324 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.148+4538A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407308 | |||||||
| chr6:89407437 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.148+4409T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407437 | |||||||
| chr6:89407448 | G | A | 3 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 |
3 | HG03130.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.148+4398C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407448 | |||||||
| chr6:89407499 | A | G | 254 | a0001c0001t0001g0162 a0001c0001t0002g0003 a0001c0001t0002g0009 others(251): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.148+4347T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407499 | |||||||
| chr6:89407591 | G | A | 2 | a0001c0001t0012g0284 a0001c0001t0012g0285 |
2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.148+4255C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407591 | |||||||
| chr6:89407678 | G | A | 3 | a0001c0001t0008g0264 a0001c0001t0008g0265 a0001c0004t0039g0235 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.148+4168C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407678 | |||||||
| chr6:89407821 | C | T | 1 | a0001c0001t0063g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.148+4025G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407821 | |||||||
| chr6:89407855 | C | T | 1 | a0001c0001t0006g0084 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.148+3991G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407855 | |||||||
| chr6:89407868 | C | T | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+3978G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89407868 | |||||||
| chr6:89408064 | CATCTGTT others(30): Show |
C | 1 | a0001c0001t0027g0243 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.148+3745_148+3781d others(39): Show |
RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408064 | |||||||
| chr6:89408087 | T | A | 1 | a0001c0001t0001g0236 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.148+3759A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408087 | |||||||
| chr6:89408225 | A | AT | 6 | a0001c0001t0007g0020 a0001c0001t0007g0268 a0001c0001t0007g0326 others(3): Show |
7 | HG01109.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3620dupA | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408225 | |||||||
| chr6:89408328 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.148+3518C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408328 | |||||||
| chr6:89408617 | A | G | 1 | a0001c0001t0043g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.148+3229T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408617 | |||||||
| chr6:89408733 | T | G | 13 | a0001c0001t0007g0020 a0001c0001t0007g0326 a0001c0001t0007g0327 others(10): Show |
14 | HG01109.hp1 HG02258.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.148+3113A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408733 | |||||||
| chr6:89408852 | A | C | 9 | a0001c0001t0004g0339 a0001c0001t0014g0006 a0001c0001t0014g0035 others(6): Show |
10 | HG01099.hp2 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.148+2994T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89408852 | |||||||
| chr6:89409045 | G | A | 39 | a0001c0001t0004g0019 a0001c0001t0004g0288 a0001c0001t0004g0290 others(36): Show |
41 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.148+2801C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409045 | |||||||
| chr6:89409135 | T | C | 335 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(332): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.148+2711A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409135 | |||||||
| chr6:89409188 | T | C | 2 | a0001c0001t0034g0071 a0001c0001t0035g0070 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.148+2658A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409188 | |||||||
| chr6:89409317 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.148+2529G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409317 | |||||||
| chr6:89409324 | A | G | 151 | a0001c0001t0001g0067 a0001c0001t0002g0009 a0001c0001t0003g0007 others(148): Show |
161 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.148+2522T>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409324 | |||||||
| chr6:89409418 | G | A | 5 | a0001c0001t0024g0338 a0001c0001t0025g0340 a0001c0001t0025g0341 others(2): Show |
5 | HG01106.hp1 HG01433.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+2428C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409418 | |||||||
| chr6:89409477 | T | G | 2 | a0001c0001t0003g0072 a0001c0001t0003g0073 |
2 | NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.148+2369A>C | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409477 | |||||||
| chr6:89409795 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.148+2051G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409795 | |||||||
| chr6:89409848 | C | T | 2 | a0001c0001t0031g0266 a0001c0001t0031g0267 |
2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.148+1998G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89409848 | |||||||
| chr6:89410295 | A | T | 1 | a0001c0002t0040g0031 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.148+1551T>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89410295 | |||||||
| chr6:89410428 | G | A | 4 | a0001c0001t0012g0312 a0001c0001t0012g0313 a0001c0001t0012g0314 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.148+1418C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89410428 | |||||||
| chr6:89410519 | C | T | 5 | a0001c0001t0015g0251 a0001c0001t0015g0252 a0001c0001t0015g0253 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+1327G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89410519 | |||||||
| chr6:89410627 | T | C | 1 | a0001c0001t0020g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.148+1219A>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89410627 | |||||||
| chr6:89411164 | G | C | 10 | a0001c0001t0004g0019 a0001c0001t0004g0316 a0001c0001t0004g0318 others(7): Show |
11 | HG01496.hp1 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.148+682C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411164 | |||||||
| chr6:89411174 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.148+672C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411174 | |||||||
| chr6:89411196 | G | C | 1 | a0001c0001t0061g0325 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.148+650C>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411196 | |||||||
| chr6:89411272 | A | C | 139 | a0001c0001t0001g0067 a0001c0001t0003g0007 a0001c0001t0003g0008 others(136): Show |
147 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.148+574T>G | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411272 | |||||||
| chr6:89411343 | C | T | 1 | a0001c0001t0010g0022 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.148+503G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411343 | |||||||
| chr6:89411370 | C | T | 18 | a0001c0001t0004g0021 a0001c0001t0004g0261 a0001c0001t0004g0339 others(15): Show |
21 | HG00735.hp1 HG01106.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.148+476G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411370 | |||||||
| chr6:89411414 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.148+432G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411414 | |||||||
| chr6:89411428 | T | A | 2 | a0001c0001t0004g0021 a0001c0001t0004g0339 |
3 | HG02723.hp2 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.148+418A>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411428 | |||||||
| chr6:89411560 | C | T | 2 | a0001c0001t0022g0249 a0001c0001t0022g0250 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.148+286G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411560 | |||||||
| chr6:89411685 | G | A | 6 | a0001c0001t0005g0017 a0001c0001t0005g0239 a0001c0001t0005g0240 others(3): Show |
7 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+161C>T | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411685 | |||||||
| chr6:89411718 | C | T | 5 | a0001c0001t0023g0246 a0001c0001t0023g0247 a0001c0001t0023g0248 others(2): Show |
5 | HG03130.hp1 HG03453.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+128G>A | RRAGD | ENSG00000025039.15 | transcript | ENST00000369415.9 | protein_coding | 1/6 | chr6 | 89411718 |