Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64121 |
| ensemblid | ENSG00000116954.8 |
| hgncid | 19902 |
| symbol | RRAGC |
| name | Ras related GTP binding C |
| refseq_nuc | NM_022157.4 |
| refseq_prot | NP_071440.1 |
| ensembl_nuc | ENST00000373001.4 |
| ensembl_prot | ENSP00000362092.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 38838198 |
| end | 38859772 |
| strand | - |
| ver | v1.2 |
| region | chr1:38838198-38859772 |
| region5000 | chr1:38833198-38864772 |
| regionname0 | RRAGC_chr1_38838198_38859772 |
| regionname5000 | RRAGC_chr1_38833198_38864772 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1197 | 403 | 87 | 65 | 192 | 18 | 39 | RRAGC_chr1_38833198_38864772 | RRAGC | ATGTC others(1192): Show |
chr1 | 38833198 | 38864772 | ||
| a0001c0002 | 0/0 | 1197 | 10 | 5 | 3 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | ATGTC others(1192): Show |
chr1 | 38833198 | 38864772 | ||
| a0001c0003 | 0/0 | 1197 | 3 | 2 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | ATGTC others(1192): Show |
chr1 | 38833198 | 38864772 | ||
| a0001c0004 | 0/0 | 1197 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | ATGTC others(1192): Show |
chr1 | 38833198 | 38864772 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2681 | 265 | 71 | 46 | 117 | 11 | 19 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0002 | 0/0 | 2681 | 73 | 0 | 8 | 55 | 0 | 10 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0003 | 0/0 | 2682 | 16 | 1 | 4 | 8 | 1 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2677): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0004 | 0/0 | 2680 | 13 | 1 | 5 | 0 | 4 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2675): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0005 | 0/0 | 2683 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2678): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0006 | 0/0 | 2681 | 9 | 9 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0007 | 1/0 | 2681 | 6 | 0 | 0 | 0 | 2 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0008 | 0/0 | 2682 | 5 | 0 | 0 | 5 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2677): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0009 | 0/0 | 2681 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0010 | 0/0 | 2682 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2677): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0011 | 0/0 | 2681 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0012 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0013 | 0/0 | 2681 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0014 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2677): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0015 | 0/0 | 2681 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0016 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0017 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0018 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0019 | 0/0 | 2681 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0020 | 0/0 | 2681 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0001t0021 | 0/0 | 2661 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2656): Show |
chr1 | 38833198 | 38864772 |
| a0001c0002t0005 | 0/0 | 2683 | 10 | 5 | 3 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2678): Show |
chr1 | 38833198 | 38864772 |
| a0001c0003t0009 | 0/0 | 2681 | 3 | 2 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| a0001c0004t0002 | 0/0 | 2681 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | GGACT others(2676): Show |
chr1 | 38833198 | 38864772 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 35 | 2 | 7 | 24 | 1 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0003 | 0/0 | 25 | 4 | 7 | 10 | 3 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0004 | 0/0 | 18 | 0 | 2 | 9 | 4 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0005 | 0/0 | 14 | 0 | 1 | 13 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0008 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0011 | 0/0 | 7 | 0 | 2 | 2 | 1 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0014 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0030 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0001 | 0/0 | 37 | 0 | 6 | 29 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0026 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0004g0007 | 0/0 | 9 | 0 | 3 | 0 | 4 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0006g0006 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0007g0013 | 1/0 | 6 | 0 | 0 | 0 | 2 | 3 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0008g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0010g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0011g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0012g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0013g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0015g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0016g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0017g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0018g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0019g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0020g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0001t0021g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0002t0005g0018 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0002t0005g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0002t0005g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0002t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0002t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0003t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0003t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0003t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| a0001c0004t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | GBR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0133 | EUR | GBR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00438 | hp2 | a0001 | c0001 | t0018 | g0110 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00597 | hp1 | a0001 | c0001 | t0016 | g0152 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01081 | hp2 | a0001 | c0001 | t0011 | g0053 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01175 | hp1 | a0001 | c0002 | t0005 | g0018 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0090 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0013 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0013 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01981 | hp2 | a0001 | c0002 | t0005 | g0018 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0020 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02165 | hp1 | a0001 | c0001 | t0012 | g0069 | EAS | CDX | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0018 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02602 | hp2 | a0001 | c0001 | t0020 | g0111 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02647 | hp2 | a0001 | c0002 | t0005 | g0063 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02698 | hp1 | a0001 | c0001 | t0015 | g0138 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0013 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02896 | hp1 | a0001 | c0002 | t0005 | g0052 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0101 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02897 | hp2 | a0001 | c0002 | t0005 | g0052 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03209 | hp2 | a0001 | c0003 | t0009 | g0056 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03540 | hp2 | a0001 | c0002 | t0005 | g0062 | AFR | GWD | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03579 | hp1 | a0001 | c0001 | t0014 | g0102 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03669 | hp1 | a0001 | c0002 | t0005 | g0032 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0013 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03927 | hp2 | a0001 | c0003 | t0009 | g0054 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG04115 | hp1 | a0001 | c0002 | t0005 | g0032 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0013 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | BEB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0098 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | CHB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18747 | hp1 | a0001 | c0001 | t0017 | g0144 | EAS | CHB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0114 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18953 | hp2 | a0001 | c0004 | t0002 | g0031 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18967 | hp2 | a0001 | c0001 | t0019 | g0097 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19006 | hp1 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | LWK | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19059 | hp1 | a0001 | c0001 | t0021 | g0140 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19059 | hp2 | a0001 | c0001 | t0008 | g0020 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19065 | hp2 | a0001 | c0004 | t0002 | g0031 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA19240 | hp2 | a0001 | c0003 | t0009 | g0055 | AFR | YRI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | TSI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | TSI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | GIH | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG01123 | hp2 | a0001 | c0002 | t0005 | g0018 | AMR | CLM | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | USA | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | USA | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0165 | REF | REF | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0013 | REF | REF | RRAGC_chr1_38833198_38864772 | RRAGC | chr1 | 38833198 | 38864772 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:38845945 | T | G | 1 | a0001c0002 | 10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
synonymous_variant | LOW | c.1042A>C | p.Arg348Arg | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/7 | 1168/2681 | 1042/1200 | 348/399 | chr1 | 38845945 | |||
| chr1:38859464 | C | T | 1 | a0001c0003 | 3 | HG03209.hp2 HG03927.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.183G>A | p.Lys61Lys | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/7 | 309/2681 | 183/1200 | 61/399 | chr1 | 38859464 | |||
| chr1:38859527 | C | T | 1 | a0001c0004 | 2 | NA18953.hp2 NA19065.hp2 |
synonymous_variant | LOW | c.120G>A | p.Ala40Ala | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/7 | 246/2681 | 120/1200 | 40/399 | chr1 | 38859527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:38838227 | A | G | 1 | a0001c0001t0018 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1326T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 1326 | chr1 | 38838227 | ||||||
| chr1:38838323 | C | T | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(13): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
3_prime_UTR_variant | MODIFIER | c.*1230G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 1230 | chr1 | 38838323 | ||||||
| chr1:38838543 | G | A | 1 | a0001c0001t0017 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1010C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 1010 | chr1 | 38838543 | ||||||
| chr1:38838575 | A | G | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(20): Show |
411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
3_prime_UTR_variant | MODIFIER | c.*978T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 978 | chr1 | 38838575 | ||||||
| chr1:38838630 | C | T | 1 | a0001c0001t0016 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*923G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 923 | chr1 | 38838630 | ||||||
| chr1:38838736 | T | C | 1 | a0001c0001t0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*817A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 817 | chr1 | 38838736 | ||||||
| chr1:38838875 | CA | C | 2 | a0001c0001t0004 a0001c0001t0013 |
14 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*677delT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 677 | chr1 | 38838875 | ||||||
| chr1:38839040 | G | C | 1 | a0001c0001t0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*513C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 513 | chr1 | 38839040 | ||||||
| chr1:38839056 | A | G | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*497T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 497 | chr1 | 38839056 | ||||||
| chr1:38839077 | C | A | 1 | a0001c0001t0014 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 476 | chr1 | 38839077 | ||||||
| chr1:38839215 | A | G | 1 | a0001c0001t0015 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 338 | chr1 | 38839215 | ||||||
| chr1:38839304 | C | A | 1 | a0001c0001t0019 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 249 | chr1 | 38839304 | ||||||
| chr1:38839330 | A | AT | 5 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0010 others(2): Show |
26 | HG00140.hp2 HG00423.hp2 HG00738.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*222dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 222 | chr1 | 38839330 | ||||||
| chr1:38839330 | A | ATT | 2 | a0001c0001t0005 a0001c0002t0005 |
11 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*221_*222dupAA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 222 | chr1 | 38839330 | ||||||
| chr1:38839407 | C | T | 1 | a0001c0001t0012 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 146 | chr1 | 38839407 | ||||||
| chr1:38839441 | T | C | 1 | a0001c0001t0020 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 112 | chr1 | 38839441 | ||||||
| chr1:38839462 | ACAAGCAG others(13): Show |
A | 1 | a0001c0001t0021 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*71_*90delGACATGGG others(12): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 71 | chr1 | 38839462 | ||||||
| chr1:38839491 | C | T | 1 | a0001c0001t0010 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 7/7 | 62 | chr1 | 38839491 | ||||||
| chr1:38859725 | C | T | 1 | a0001c0001t0011 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/7 | 79 | chr1 | 38859725 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:38839731 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(13): Show |
36 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1049-27G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38839731 | |||||||
| chr1:38840147 | C | CA | 5 | a0001c0001t0001g0084 a0001c0001t0002g0025 a0001c0001t0002g0112 others(2): Show |
15 | HG02055.hp1 HG02559.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1049-444dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840147 | |||||||
| chr1:38840401 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1049-697T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840401 | |||||||
| chr1:38840402 | C | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1049-698G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840402 | |||||||
| chr1:38840409 | C | G | 2 | a0001c0001t0006g0006 a0001c0001t0014g0102 |
10 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-705G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840409 | |||||||
| chr1:38840410 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0036 others(6): Show |
22 | HG01069.hp2 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1049-706C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840410 | |||||||
| chr1:38840482 | G | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0128 others(4): Show |
9 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1049-778C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840482 | |||||||
| chr1:38840800 | G | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0037 others(8): Show |
30 | HG00323.hp1 HG00741.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1049-1096C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840800 | |||||||
| chr1:38840816 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1049-1112T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840816 | |||||||
| chr1:38840973 | A | G | 4 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0062 others(1): Show |
8 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1269T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38840973 | |||||||
| chr1:38841367 | A | T | 1 | a0001c0001t0005g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1049-1663T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841367 | |||||||
| chr1:38841368 | A | AT | 9 | a0001c0001t0001g0049 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
13 | HG02109.hp2 HG02738.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1049-1665dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841368 | |||||||
| chr1:38841368 | A | ATT | 34 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(31): Show |
96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1049-1666_1049-166 others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841368 | |||||||
| chr1:38841368 | A | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(14): Show |
37 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1049-1664T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841368 | |||||||
| chr1:38841368 | AT | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0037 |
7 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-1665delA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841368 | |||||||
| chr1:38841476 | G | A | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0128 others(4): Show |
9 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1049-1772C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841476 | |||||||
| chr1:38841603 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(33): Show |
98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1049-1899C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841603 | |||||||
| chr1:38841675 | A | T | 4 | a0001c0001t0009g0101 a0001c0003t0009g0054 a0001c0003t0009g0055 others(1): Show |
4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049-1971T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841675 | |||||||
| chr1:38841676 | T | A | 4 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0062 others(1): Show |
8 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1972A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841676 | |||||||
| chr1:38841677 | T | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0134 |
8 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1049-1973A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841677 | |||||||
| chr1:38841865 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1049-2161C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38841865 | |||||||
| chr1:38842000 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1049-2296A>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842000 | |||||||
| chr1:38842055 | G | A | 8 | a0001c0001t0001g0057 a0001c0001t0004g0007 a0001c0001t0004g0091 others(5): Show |
17 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1049-2351C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842055 | |||||||
| chr1:38842205 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1049-2501C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842205 | |||||||
| chr1:38842287 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01884.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1049-2583G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842287 | |||||||
| chr1:38842612 | G | C | 1 | a0001c0001t0014g0102 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1049-2908C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842612 | |||||||
| chr1:38842628 | T | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
5 | HG02818.hp2 HG03098.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049-2924A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842628 | |||||||
| chr1:38842976 | A | G | 8 | a0001c0001t0001g0057 a0001c0001t0004g0007 a0001c0001t0004g0091 others(5): Show |
17 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1048+2963T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38842976 | |||||||
| chr1:38843366 | C | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0061 |
7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+2573G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843366 | |||||||
| chr1:38843435 | T | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(42): Show |
112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1048+2504A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843435 | |||||||
| chr1:38843443 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1048+2496C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843443 | |||||||
| chr1:38843492 | A | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(38): Show |
104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1048+2447T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843492 | |||||||
| chr1:38843545 | C | T | 1 | a0001c0001t0009g0101 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1048+2394G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843545 | |||||||
| chr1:38843562 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(13): Show |
36 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1048+2377A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843562 | |||||||
| chr1:38843645 | G | A | 4 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0062 others(1): Show |
8 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+2294C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843645 | |||||||
| chr1:38843693 | C | A | 1 | a0001c0001t0001g0028 | 3 | HG00621.hp1 HG02683.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1048+2246G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843693 | |||||||
| chr1:38843717 | C | CA | 7 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0001g0160 others(4): Show |
12 | HG00741.hp2 HG01952.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048+2221dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843717 | |||||||
| chr1:38843738 | G | C | 1 | a0001c0002t0005g0032 | 2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1048+2201C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843738 | |||||||
| chr1:38843817 | T | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+2122A>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843817 | |||||||
| chr1:38843938 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1048+2001A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843938 | |||||||
| chr1:38843970 | A | C | 1 | a0001c0001t0002g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1048+1969T>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38843970 | |||||||
| chr1:38844012 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0061 |
7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+1927A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844012 | |||||||
| chr1:38844031 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1048+1908T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844031 | |||||||
| chr1:38844269 | T | C | 1 | a0001c0001t0002g0107 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1048+1670A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844269 | |||||||
| chr1:38844309 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG01099.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1048+1630G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844309 | |||||||
| chr1:38844409 | C | T | 6 | a0001c0001t0004g0007 a0001c0001t0004g0091 a0001c0001t0004g0092 others(3): Show |
14 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1048+1530G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844409 | |||||||
| chr1:38844447 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+1492C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844447 | |||||||
| chr1:38844448 | G | A | 1 | a0001c0001t0001g0044 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1048+1491C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844448 | |||||||
| chr1:38844448 | G | GA | 9 | a0001c0001t0001g0081 a0001c0001t0001g0143 a0001c0001t0002g0124 others(6): Show |
17 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1048+1490dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844448 | |||||||
| chr1:38844448 | GA | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0001g0082 others(2): Show |
11 | HG02071.hp1 HG02155.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1048+1490delT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844448 | |||||||
| chr1:38844487 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0128 others(4): Show |
9 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+1452G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844487 | |||||||
| chr1:38844539 | G | C | 1 | a0001c0001t0002g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1048+1400C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844539 | |||||||
| chr1:38844593 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0080 |
8 | HG02109.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048+1346A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844593 | |||||||
| chr1:38844728 | A | G | 2 | a0001c0001t0003g0026 a0001c0001t0003g0136 |
4 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+1211T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844728 | |||||||
| chr1:38844730 | C | G | 2 | a0001c0001t0001g0070 a0001c0001t0012g0069 |
2 | HG00408.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1048+1209G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844730 | |||||||
| chr1:38844758 | C | T | 1 | a0001c0001t0001g0049 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1048+1181G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844758 | |||||||
| chr1:38844807 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1048+1132C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844807 | |||||||
| chr1:38844833 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1048+1106A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844833 | |||||||
| chr1:38844967 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(49): Show |
130 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1048+972T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38844967 | |||||||
| chr1:38845137 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1048+802C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845137 | |||||||
| chr1:38845178 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0067 a0001c0001t0001g0081 others(2): Show |
7 | HG00639.hp2 HG01243.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+761T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845178 | |||||||
| chr1:38845185 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0061 |
7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+754A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845185 | |||||||
| chr1:38845214 | C | T | 1 | a0001c0001t0001g0033 | 2 | NA18941.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1048+725G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845214 | |||||||
| chr1:38845419 | T | C | 3 | a0001c0001t0002g0042 a0001c0001t0002g0106 a0001c0001t0002g0118 |
4 | HG03491.hp2 HG03831.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+520A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845419 | |||||||
| chr1:38845437 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1048+502C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845437 | |||||||
| chr1:38845627 | AT | A | 1 | a0001c0001t0001g0027 | 3 | NA18950.hp2 NA18984.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1048+311delA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845627 | |||||||
| chr1:38845698 | A | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0136 |
4 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+241T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845698 | |||||||
| chr1:38845709 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1048+230A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845709 | |||||||
| chr1:38845765 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1048+174C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845765 | |||||||
| chr1:38845853 | C | T | 5 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0052 others(2): Show |
10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1048+86G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845853 | |||||||
| chr1:38845862 | T | C | 1 | a0001c0001t0001g0016 | 5 | HG00741.hp2 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048+77A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 6/6 | chr1 | 38845862 | |||||||
| chr1:38846119 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0061 |
7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.900-32C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846119 | |||||||
| chr1:38846196 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.900-109T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846196 | |||||||
| chr1:38846326 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(33): Show |
98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.900-239C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846326 | |||||||
| chr1:38846472 | A | AC | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.900-386dupG | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846472 | |||||||
| chr1:38846487 | C | T | 1 | a0001c0001t0001g0028 | 3 | HG00621.hp1 HG02683.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.900-400G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846487 | |||||||
| chr1:38846488 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(47): Show |
132 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.900-401C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846488 | |||||||
| chr1:38846569 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.900-482G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846569 | |||||||
| chr1:38846667 | C | T | 1 | a0001c0001t0010g0024 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.900-580G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846667 | |||||||
| chr1:38846668 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.900-581C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846668 | |||||||
| chr1:38846747 | T | C | 5 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0052 others(2): Show |
10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.900-660A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846747 | |||||||
| chr1:38846873 | C | T | 4 | a0001c0001t0009g0101 a0001c0003t0009g0054 a0001c0003t0009g0055 others(1): Show |
4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-786G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846873 | |||||||
| chr1:38846948 | T | C | 1 | a0001c0001t0003g0136 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.900-861A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846948 | |||||||
| chr1:38846962 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.900-875A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38846962 | |||||||
| chr1:38847003 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(37): Show |
103 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.900-916C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847003 | |||||||
| chr1:38847178 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.900-1091G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847178 | |||||||
| chr1:38847215 | T | C | 36 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(33): Show |
98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.900-1128A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847215 | |||||||
| chr1:38847359 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-1272G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847359 | |||||||
| chr1:38847410 | G | C | 1 | a0001c0001t0006g0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-1323C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847410 | |||||||
| chr1:38847413 | C | A | 1 | a0001c0001t0006g0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-1326G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847413 | |||||||
| chr1:38847415 | GCCTAGGC | G | 1 | a0001c0001t0006g0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.900-1335_900-1329d others(9): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847415 | |||||||
| chr1:38847427 | CAAGA | C | 1 | a0001c0001t0006g0006 | 8 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.900-1344_900-1341d others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847427 | |||||||
| chr1:38847431 | A | AAC | 17 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0016 others(14): Show |
26 | HG00642.hp2 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.900-1346_900-1345d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | |||||||
| chr1:38847431 | A | AACAC | 4 | a0001c0001t0003g0026 a0001c0001t0003g0136 a0001c0001t0010g0024 others(1): Show |
8 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.900-1348_900-1345d others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | |||||||
| chr1:38847431 | A | AACACAC | 7 | a0001c0001t0001g0044 a0001c0001t0001g0128 a0001c0001t0001g0130 others(4): Show |
15 | HG00099.hp1 HG00639.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.900-1350_900-1345d others(8): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | |||||||
| chr1:38847431 | A | AACACACA others(1): Show |
4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0004g0091 others(1): Show |
4 | HG01167.hp1 HG01346.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-1352_900-1345d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | |||||||
| chr1:38847431 | A | AACACACA others(3): Show |
2 | a0001c0001t0001g0057 a0001c0001t0004g0007 |
2 | HG02280.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.900-1354_900-1345d others(12): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | |||||||
| chr1:38847431 | A | AACACACA others(5): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0129 |
3 | HG02257.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.900-1356_900-1345d others(14): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | |||||||
| chr1:38847431 | AAC | A | 3 | a0001c0002t0005g0018 a0001c0002t0005g0062 a0001c0002t0005g0063 |
3 | HG02257.hp2 HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.900-1346_900-1345d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | |||||||
| chr1:38847431 | AACACACA others(1): Show |
A | 2 | a0001c0002t0005g0018 a0001c0002t0005g0032 |
5 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.900-1352_900-1345d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847431 | |||||||
| chr1:38847503 | G | A | 2 | a0001c0001t0006g0006 a0001c0001t0014g0102 |
10 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.900-1416C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847503 | |||||||
| chr1:38847556 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(37): Show |
103 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.900-1469C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847556 | |||||||
| chr1:38847560 | A | AT | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.900-1474dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847560 | |||||||
| chr1:38847577 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0074 others(3): Show |
12 | HG01069.hp2 HG02572.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.900-1490C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847577 | |||||||
| chr1:38847626 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(11): Show |
32 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.900-1539G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847626 | |||||||
| chr1:38847915 | C | T | 1 | a0001c0001t0004g0091 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.900-1828G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847915 | |||||||
| chr1:38847928 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.900-1841C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38847928 | |||||||
| chr1:38848027 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.900-1940G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848027 | |||||||
| chr1:38848033 | C | CA | 90 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.900-1947dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848033 | |||||||
| chr1:38848033 | C | CAA | 5 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
9 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.900-1948_900-1947d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848033 | |||||||
| chr1:38848033 | C | CAAA | 9 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(6): Show |
19 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.900-1949_900-1947d others(5): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848033 | |||||||
| chr1:38848377 | C | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0089 |
2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.900-2290G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848377 | |||||||
| chr1:38848525 | T | C | 5 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0052 others(2): Show |
10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.900-2438A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848525 | |||||||
| chr1:38848613 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.900-2526T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848613 | |||||||
| chr1:38848672 | T | C | 1 | a0001c0003t0009g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.900-2585A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848672 | |||||||
| chr1:38848796 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0061 |
7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.900-2709C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848796 | |||||||
| chr1:38848909 | A | G | 2 | a0001c0001t0002g0109 a0001c0004t0002g0031 |
3 | NA18953.hp2 NA19065.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.899+2706T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848909 | |||||||
| chr1:38848965 | C | G | 1 | a0001c0001t0002g0108 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.899+2650G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38848965 | |||||||
| chr1:38849029 | C | T | 1 | a0001c0001t0006g0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.899+2586G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849029 | |||||||
| chr1:38849286 | T | C | 5 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0052 others(2): Show |
10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.899+2329A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849286 | |||||||
| chr1:38849422 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.899+2193G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849422 | |||||||
| chr1:38849612 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(46): Show |
123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.899+2003G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849612 | |||||||
| chr1:38849613 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.899+2002C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849613 | |||||||
| chr1:38849666 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.899+1949G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849666 | |||||||
| chr1:38849752 | A | G | 2 | a0001c0001t0003g0026 a0001c0001t0003g0136 |
4 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+1863T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849752 | |||||||
| chr1:38849763 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.899+1852C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849763 | |||||||
| chr1:38849824 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.899+1791T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849824 | |||||||
| chr1:38849936 | G | A | 1 | a0001c0002t0005g0052 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.899+1679C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849936 | |||||||
| chr1:38849955 | C | T | 2 | a0001c0003t0009g0055 a0001c0003t0009g0056 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.899+1660G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849955 | |||||||
| chr1:38849959 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0162 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.899+1656G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849959 | |||||||
| chr1:38849971 | C | T | 1 | a0001c0001t0010g0024 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1644G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849971 | |||||||
| chr1:38849972 | C | T | 1 | a0001c0001t0010g0024 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1643G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849972 | |||||||
| chr1:38849973 | A | G | 1 | a0001c0001t0010g0024 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1642T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849973 | |||||||
| chr1:38849974 | C | A | 1 | a0001c0001t0010g0024 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1641G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849974 | |||||||
| chr1:38849977 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.899+1638G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849977 | |||||||
| chr1:38849980 | G | GCCACC | 1 | a0001c0001t0010g0024 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1634_899+1635i others(7): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849980 | |||||||
| chr1:38849982 | GGA | G | 1 | a0001c0001t0010g0024 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1631_899+1632d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849982 | |||||||
| chr1:38849987 | A | T | 1 | a0001c0001t0010g0024 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1628T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849987 | |||||||
| chr1:38849988 | C | T | 1 | a0001c0001t0010g0024 | 3 | HG02055.hp2 HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.899+1627G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38849988 | |||||||
| chr1:38850092 | G | A | 2 | a0001c0001t0004g0091 a0001c0001t0004g0092 |
2 | HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.899+1523C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850092 | |||||||
| chr1:38850121 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.899+1494C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850121 | |||||||
| chr1:38850133 | G | C | 1 | a0001c0001t0004g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.899+1482C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850133 | |||||||
| chr1:38850138 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.899+1477C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850138 | |||||||
| chr1:38850143 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.899+1472A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850143 | |||||||
| chr1:38850203 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.899+1412A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850203 | |||||||
| chr1:38850276 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.899+1339G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850276 | |||||||
| chr1:38850307 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0137 others(8): Show |
21 | HG00408.hp1 HG00597.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.899+1308C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850307 | |||||||
| chr1:38850329 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(11): Show |
32 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.899+1286T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850329 | |||||||
| chr1:38850383 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.899+1232C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850383 | |||||||
| chr1:38850390 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(13): Show |
36 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.899+1225A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850390 | |||||||
| chr1:38850427 | T | C | 1 | a0001c0001t0001g0044 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.899+1188A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850427 | |||||||
| chr1:38850436 | C | G | 1 | a0001c0002t0005g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.899+1179G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850436 | |||||||
| chr1:38850440 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.899+1175C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850440 | |||||||
| chr1:38850493 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.899+1122C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850493 | |||||||
| chr1:38850512 | T | TAATA | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(32): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.899+1099_899+1102d others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850512 | |||||||
| chr1:38850512 | T | TAATAAAT others(1): Show |
11 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0051 others(8): Show |
19 | HG02055.hp2 HG02109.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.899+1095_899+1102d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850512 | |||||||
| chr1:38850512 | TAATA | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
37 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.899+1099_899+1102d others(6): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850512 | |||||||
| chr1:38850512 | TAATAAAT others(1): Show |
T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0074 others(3): Show |
12 | HG01069.hp2 HG02572.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.899+1095_899+1102d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850512 | |||||||
| chr1:38850581 | T | G | 1 | a0001c0001t0006g0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.899+1034A>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850581 | |||||||
| chr1:38850591 | T | C | 1 | a0001c0001t0002g0120 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.899+1024A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850591 | |||||||
| chr1:38850637 | GA | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0129 |
3 | HG02257.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.899+977delT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850637 | |||||||
| chr1:38850639 | A | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0129 |
3 | HG02257.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.899+976T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850639 | |||||||
| chr1:38850667 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.899+948T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850667 | |||||||
| chr1:38850783 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.899+832A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850783 | |||||||
| chr1:38850843 | TG | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(46): Show |
123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.899+771delC | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850843 | |||||||
| chr1:38850844 | G | GT | 7 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0045 others(4): Show |
13 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.899+770dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850844 | |||||||
| chr1:38850845 | T | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(46): Show |
123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.899+770A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850845 | |||||||
| chr1:38850971 | T | A | 2 | a0001c0001t0002g0025 a0001c0001t0002g0122 |
4 | NA18953.hp1 NA18954.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.899+644A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38850971 | |||||||
| chr1:38851244 | C | T | 1 | a0001c0001t0017g0144 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.899+371G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38851244 | |||||||
| chr1:38851279 | T | TTAAA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.899+332_899+335dup others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38851279 | |||||||
| chr1:38851429 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.899+186G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38851429 | |||||||
| chr1:38851491 | G | C | 4 | a0001c0001t0009g0101 a0001c0003t0009g0054 a0001c0003t0009g0055 others(1): Show |
4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+124C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 5/6 | chr1 | 38851491 | |||||||
| chr1:38851897 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.757-140G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 4/6 | chr1 | 38851897 | |||||||
| chr1:38852038 | A | T | 1 | a0001c0001t0014g0102 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.757-281T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 4/6 | chr1 | 38852038 | |||||||
| chr1:38852131 | A | T | 1 | a0001c0001t0001g0072 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.756+243T>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 4/6 | chr1 | 38852131 | |||||||
| chr1:38852332 | A | G | 4 | a0001c0001t0009g0101 a0001c0003t0009g0054 a0001c0003t0009g0055 others(1): Show |
4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.756+42T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 4/6 | chr1 | 38852332 | |||||||
| chr1:38852752 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.642-264C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852752 | |||||||
| chr1:38852803 | C | T | 1 | a0001c0001t0001g0022 | 3 | NA18939.hp2 NA18977.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.642-315G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852803 | |||||||
| chr1:38852935 | C | G | 1 | a0001c0001t0003g0136 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.642-447G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852935 | |||||||
| chr1:38852942 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.642-454G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852942 | |||||||
| chr1:38852967 | A | G | 5 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0052 others(2): Show |
10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.642-479T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38852967 | |||||||
| chr1:38853106 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0012g0069 |
2 | HG00408.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.642-618T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853106 | |||||||
| chr1:38853299 | G | A | 1 | a0001c0001t0019g0097 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.642-811C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853299 | |||||||
| chr1:38853321 | A | C | 5 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0052 others(2): Show |
10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.642-833T>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853321 | |||||||
| chr1:38853337 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(38): Show |
104 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.642-849G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853337 | |||||||
| chr1:38853366 | G | T | 6 | a0001c0001t0004g0007 a0001c0001t0004g0091 a0001c0001t0004g0092 others(3): Show |
14 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.642-878C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853366 | |||||||
| chr1:38853545 | A | C | 1 | a0001c0001t0006g0006 | 9 | HG02055.hp1 HG02559.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.642-1057T>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853545 | |||||||
| chr1:38853571 | C | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0045 |
7 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.642-1083G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853571 | |||||||
| chr1:38853575 | A | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(59): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.642-1087T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853575 | |||||||
| chr1:38853578 | T | A | 1 | a0001c0002t0005g0052 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.642-1090A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853578 | |||||||
| chr1:38853688 | G | A | 7 | a0001c0001t0001g0057 a0001c0001t0004g0007 a0001c0001t0004g0091 others(4): Show |
15 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.642-1200C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853688 | |||||||
| chr1:38853708 | T | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0122 |
4 | NA18953.hp1 NA18954.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-1220A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853708 | |||||||
| chr1:38853747 | C | CA | 9 | a0001c0001t0001g0068 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
9 | HG02572.hp1 HG02602.hp1 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.642-1260dupT | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853747 | |||||||
| chr1:38853753 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.642-1265T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853753 | |||||||
| chr1:38853806 | A | G | 4 | a0001c0001t0009g0101 a0001c0003t0009g0054 a0001c0003t0009g0055 others(1): Show |
4 | HG02896.hp2 HG03209.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-1318T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853806 | |||||||
| chr1:38853932 | G | A | 1 | a0001c0002t0005g0052 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.642-1444C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853932 | |||||||
| chr1:38853953 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.642-1465T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38853953 | |||||||
| chr1:38854039 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.642-1551A>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854039 | |||||||
| chr1:38854065 | C | CT | 5 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0001c0001t0002g0040 others(2): Show |
6 | HG02622.hp2 HG04184.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.642-1578dupA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854065 | |||||||
| chr1:38854065 | CT | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.642-1578delA | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854065 | |||||||
| chr1:38854065 | CTT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0099 others(8): Show |
25 | HG01069.hp2 HG01070.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.642-1579_642-1578d others(4): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854065 | |||||||
| chr1:38854194 | A | G | 1 | a0001c0001t0002g0104 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.641+1514T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854194 | |||||||
| chr1:38854257 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0134 a0001c0001t0001g0135 |
4 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+1451G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854257 | |||||||
| chr1:38854344 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.641+1364A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854344 | |||||||
| chr1:38854358 | T | C | 1 | a0001c0001t0001g0038 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.641+1350A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854358 | |||||||
| chr1:38854394 | T | C | 1 | a0001c0001t0003g0050 | 2 | NA18952.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.641+1314A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854394 | |||||||
| chr1:38854421 | T | TTGTTA | 5 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0052 others(2): Show |
10 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.641+1286_641+1287i others(7): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854421 | |||||||
| chr1:38854637 | C | T | 1 | a0001c0001t0015g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.641+1071G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854637 | |||||||
| chr1:38854733 | C | T | 1 | a0001c0001t0001g0021 | 4 | HG02630.hp1 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+975G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854733 | |||||||
| chr1:38854843 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.641+865G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854843 | |||||||
| chr1:38854846 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0134 a0001c0001t0001g0135 |
4 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+862C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854846 | |||||||
| chr1:38854920 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.641+788G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38854920 | |||||||
| chr1:38855318 | TAAGACTC others(6): Show |
T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
5 | HG02257.hp1 HG02922.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+377_641+389del others(13): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38855318 | |||||||
| chr1:38855456 | CTT | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0061 |
7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.641+250_641+251del others(2): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 3/6 | chr1 | 38855456 | |||||||
| chr1:38856041 | A | G | 1 | a0001c0001t0002g0039 | 2 | NA19007.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.442-134T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856041 | |||||||
| chr1:38856250 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.442-343A>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856250 | |||||||
| chr1:38856334 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.442-427G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856334 | |||||||
| chr1:38856651 | C | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.441+228G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856651 | |||||||
| chr1:38856798 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.441+81A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 2/6 | chr1 | 38856798 | |||||||
| chr1:38857301 | C | A | 1 | a0001c0001t0001g0100 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.238-219G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857301 | |||||||
| chr1:38857555 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.238-473C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857555 | |||||||
| chr1:38857683 | G | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
36 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.238-601C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857683 | |||||||
| chr1:38857758 | G | A | 1 | a0001c0001t0014g0102 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.238-676C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857758 | |||||||
| chr1:38857841 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.238-759A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38857841 | |||||||
| chr1:38858126 | CGTACCCA others(1): Show |
C | 4 | a0001c0002t0005g0018 a0001c0002t0005g0032 a0001c0002t0005g0062 others(1): Show |
8 | HG01123.hp2 HG01175.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-1052_238-1045d others(10): Show |
RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858126 | |||||||
| chr1:38858197 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.238-1115T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858197 | |||||||
| chr1:38858312 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.237+1098C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858312 | |||||||
| chr1:38858372 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.237+1038C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858372 | |||||||
| chr1:38858381 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0061 |
7 | HG00642.hp2 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.237+1029G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858381 | |||||||
| chr1:38858469 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0045 |
7 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.237+941G>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858469 | |||||||
| chr1:38858613 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.237+797T>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858613 | |||||||
| chr1:38858721 | C | A | 1 | a0001c0001t0002g0126 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.237+689G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858721 | |||||||
| chr1:38858827 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.237+583C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858827 | |||||||
| chr1:38858878 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.237+532C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858878 | |||||||
| chr1:38858940 | A | C | 1 | a0001c0001t0002g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.237+470T>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38858940 | |||||||
| chr1:38859051 | G | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0128 others(4): Show |
9 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.237+359C>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859051 | |||||||
| chr1:38859141 | G | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0136 |
4 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+269C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859141 | |||||||
| chr1:38859143 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.237+267C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859143 | |||||||
| chr1:38859187 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(54): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.237+223G>C | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859187 | |||||||
| chr1:38859220 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.237+190C>A | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859220 | |||||||
| chr1:38859342 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0174 |
4 | HG01070.hp2 HG02683.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+68C>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859342 | |||||||
| chr1:38859345 | C | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
11 | HG01069.hp1 HG01071.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.237+65G>T | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859345 | |||||||
| chr1:38859391 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(55): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.237+19A>G | RRAGC | ENSG00000116954.8 | transcript | ENST00000373001.4 | protein_coding | 1/6 | chr1 | 38859391 |