Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 49856 |
| ensemblid | ENSG00000116213.16 |
| hgncid | 12759 |
| symbol | WRAP73 |
| name | WD repeat containing, antisense to TP73 |
| refseq_nuc | NM_017818.4 |
| refseq_prot | NP_060288.3 |
| ensembl_nuc | ENST00000270708.12 |
| ensembl_prot | ENSP00000270708.7 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 3630770 |
| end | 3650103 |
| strand | - |
| ver | v1.2 |
| region | chr1:3630770-3650103 |
| region5000 | chr1:3625770-3655103 |
| regionname0 | WRAP73_chr1_3630770_3650103 |
| regionname5000 | WRAP73_chr1_3625770_3655103 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 460 | 338 | 78 | 58 | 145 | 17 | 38 | 100 | WRAP73_chr1_3625770_3655103 | WRAP73 | MNFSE others(455): Show |
chr1 | 3625770 | 3655103 |
| a0002 | 0/0 | 460 | 23 | 4 | 14 | 0 | 1 | 4 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | MNFSE others(455): Show |
chr1 | 3625770 | 3655103 |
| a0003 | 0/0 | 460 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | MNFSE others(455): Show |
chr1 | 3625770 | 3655103 |
| a0004 | 0/0 | 460 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | MNFSE others(455): Show |
chr1 | 3625770 | 3655103 |
| a0005 | 0/0 | 460 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | MNFSE others(455): Show |
chr1 | 3625770 | 3655103 |
| a0006 | 0/0 | 460 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | MNFSE others(455): Show |
chr1 | 3625770 | 3655103 |
| a0007 | 0/0 | 460 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | MNFSE others(455): Show |
chr1 | 3625770 | 3655103 |
| a0008 | 0/0 | 460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | MNFSE others(455): Show |
chr1 | 3625770 | 3655103 |
| a0009 | 0/0 | 460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | MNFSE others(455): Show |
chr1 | 3625770 | 3655103 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1380 | 263 | 60 | 41 | 117 | 13 | 31 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0001c0002 | 0/0 | 1380 | 41 | 1 | 4 | 28 | 1 | 7 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0001c0003 | 1/0 | 1380 | 28 | 11 | 13 | 0 | 3 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0001c0006 | 0/0 | 1380 | 5 | 5 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0001c0013 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0002c0004 | 0/0 | 1380 | 23 | 4 | 14 | 0 | 1 | 4 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0003c0005 | 0/0 | 1380 | 10 | 9 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0004c0007 | 0/0 | 1380 | 3 | 3 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0004c0008 | 0/0 | 1380 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0005c0009 | 0/0 | 1380 | 2 | 0 | 2 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0006c0014 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0007c0010 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0008c0011 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 | ||
| a0009c0012 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | ATGAA others(1375): Show |
chr1 | 3625770 | 3655103 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1692 | 130 | 48 | 15 | 52 | 3 | 12 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0001c0001t0002 | 0/1 | 1684 | 126 | 9 | 25 | 63 | 10 | 18 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1679): Show |
chr1 | 3625770 | 3655103 |
| a0001c0001t0003 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0001c0001t0004 | 0/0 | 1684 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1679): Show |
chr1 | 3625770 | 3655103 |
| a0001c0001t0005 | 0/0 | 1684 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1679): Show |
chr1 | 3625770 | 3655103 |
| a0001c0001t0008 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0001c0001t0009 | 0/0 | 1684 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1679): Show |
chr1 | 3625770 | 3655103 |
| a0001c0002t0001 | 0/0 | 1692 | 41 | 1 | 4 | 28 | 1 | 7 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0001c0003t0001 | 1/0 | 1692 | 27 | 10 | 13 | 0 | 3 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0001c0003t0006 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0001c0006t0001 | 0/0 | 1692 | 5 | 5 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0001c0013t0001 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0002c0004t0001 | 0/0 | 1692 | 23 | 4 | 14 | 0 | 1 | 4 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0003c0005t0001 | 0/0 | 1692 | 9 | 8 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0003c0005t0007 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0004c0007t0001 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0004c0008t0001 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0005c0009t0002 | 0/0 | 1684 | 2 | 0 | 2 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1679): Show |
chr1 | 3625770 | 3655103 |
| a0006c0014t0001 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0007c0010t0002 | 0/0 | 1684 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1679): Show |
chr1 | 3625770 | 3655103 |
| a0008c0011t0001 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| a0009c0012t0001 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | GACTT others(1687): Show |
chr1 | 3625770 | 3655103 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 40 | 1 | 1 | 34 | 1 | 3 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0007 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0001 | 0/0 | 73 | 4 | 17 | 37 | 5 | 10 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0008g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0001t0009g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0004 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0005 | 0/0 | 8 | 0 | 0 | 7 | 1 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0009 | 0/0 | 5 | 1 | 1 | 0 | 0 | 3 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0011 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0003t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0006t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0006t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0006t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0001c0013t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0002c0004t0001g0003 | 0/0 | 16 | 1 | 12 | 0 | 1 | 2 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0002c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0002c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0002c0004t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0002c0004t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0002c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0002c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0003c0005t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0003c0005t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0003c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0003c0005t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0003c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0003c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0003c0005t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0004c0007t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0004c0007t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0004c0008t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0005c0009t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0006c0014t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0007c0010t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0008c0011t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| a0009c0012t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0160 | EUR | GBR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | GBR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0124 | EUR | FIN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0005 | EUR | FIN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | FIN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00609 | hp2 | a0006 | c0014 | t0001 | g0129 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00642 | hp2 | a0002 | c0004 | t0001 | g0003 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00733 | hp1 | a0002 | c0004 | t0001 | g0003 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00733 | hp2 | a0001 | c0001 | t0009 | g0141 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0067 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01081 | hp1 | a0007 | c0010 | t0002 | g0150 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01081 | hp2 | a0002 | c0004 | t0001 | g0089 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01109 | hp2 | a0003 | c0005 | t0001 | g0051 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01168 | hp2 | a0005 | c0009 | t0002 | g0037 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01169 | hp2 | a0005 | c0009 | t0002 | g0037 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0058 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01257 | hp1 | a0002 | c0004 | t0001 | g0003 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01258 | hp1 | a0002 | c0004 | t0001 | g0003 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0118 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0063 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0024 | EUR | IBS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0024 | EUR | IBS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01884 | hp1 | a0003 | c0005 | t0001 | g0014 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01928 | hp1 | a0002 | c0004 | t0001 | g0003 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01934 | hp2 | a0002 | c0004 | t0001 | g0003 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01952 | hp1 | a0002 | c0004 | t0001 | g0003 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01952 | hp2 | a0002 | c0004 | t0001 | g0088 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01975 | hp2 | a0002 | c0004 | t0001 | g0003 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01981 | hp1 | a0002 | c0004 | t0001 | g0003 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01993 | hp2 | a0002 | c0004 | t0001 | g0003 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02145 | hp2 | a0003 | c0005 | t0001 | g0052 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02148 | hp1 | a0002 | c0004 | t0001 | g0003 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CDX | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02257 | hp1 | a0002 | c0004 | t0001 | g0116 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02273 | hp2 | a0002 | c0004 | t0001 | g0003 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02572 | hp2 | a0003 | c0005 | t0001 | g0021 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02615 | hp2 | a0001 | c0013 | t0001 | g0060 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02647 | hp1 | a0003 | c0005 | t0001 | g0053 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02717 | hp2 | a0002 | c0004 | t0001 | g0003 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02723 | hp1 | a0004 | c0007 | t0001 | g0117 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0140 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0056 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02886 | hp1 | a0004 | c0008 | t0001 | g0026 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02896 | hp1 | a0002 | c0004 | t0001 | g0030 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02897 | hp1 | a0002 | c0004 | t0001 | g0030 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02922 | hp2 | a0003 | c0005 | t0007 | g0139 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0071 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02970 | hp2 | a0004 | c0008 | t0001 | g0026 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0072 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0057 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03098 | hp2 | a0004 | c0007 | t0001 | g0027 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03130 | hp2 | a0003 | c0005 | t0001 | g0049 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0015 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0015 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03486 | hp2 | a0001 | c0003 | t0006 | g0119 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03516 | hp2 | a0008 | c0011 | t0001 | g0050 | AFR | ESN | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03654 | hp2 | a0002 | c0004 | t0001 | g0115 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03834 | hp2 | a0002 | c0004 | t0001 | g0087 | SAS | BEB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04184 | hp1 | a0002 | c0004 | t0001 | g0003 | SAS | BEB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | BEB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18522 | hp1 | a0009 | c0012 | t0001 | g0074 | AFR | YRI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18906 | hp1 | a0003 | c0005 | t0001 | g0021 | AFR | YRI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19030 | hp1 | a0003 | c0005 | t0001 | g0014 | AFR | LWK | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19043 | hp1 | a0003 | c0005 | t0001 | g0014 | AFR | LWK | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA19240 | hp2 | a0001 | c0006 | t0001 | g0015 | AFR | YRI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ASW | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20752 | hp2 | a0002 | c0004 | t0001 | g0003 | EUR | TSI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20905 | hp1 | a0002 | c0004 | t0001 | g0003 | SAS | GIH | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | GIH | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0062 | AMR | CLM | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | USA | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | USA | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| NA21309 | hp2 | a0004 | c0007 | t0001 | g0027 | AFR | LWK | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0169 | REF | REF | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0086 | REF | REF | WRAP73_chr1_3625770_3655103 | WRAP73 | chr1 | 3625770 | 3655103 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:3630772 | G | A | 1 | a0001 | 2 | NA19011.hp1 NA19080.hp1 |
splice_region_variant | LOW | c.*203C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 12/12 | chr1 | 3630772 | |||||||
| chr1:3631486 | G | A | 2 | a0003 a0008 |
11 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
missense_variant | MODERATE | c.1220C>T | p.Ser407Leu | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 11/12 | 1324/1692 | 1220/1383 | 407/460 | chr1 | 3631486 | |||
| chr1:3631558 | G | A | 1 | a0005 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.1148C>T | p.Pro383Leu | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 11/12 | 1252/1692 | 1148/1383 | 383/460 | chr1 | 3631558 | |||
| chr1:3631634 | C | T | 1 | a0004 | 5 | HG02723.hp1 HG02886.hp1 HG02970.hp2 others(2): Show |
missense_variant | MODERATE | c.1072G>A | p.Val358Ile | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 11/12 | 1176/1692 | 1072/1383 | 358/460 | chr1 | 3631634 | |||
| chr1:3631640 | C | T | 1 | a0009 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.1066G>A | p.Val356Ile | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 11/12 | 1170/1692 | 1066/1383 | 356/460 | chr1 | 3631640 | |||
| chr1:3632268 | G | C | 1 | a0002 | 23 | HG00642.hp2 HG00733.hp1 HG01081.hp2 others(20): Show |
missense_variant | MODERATE | c.993C>G | p.Ile331Met | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/12 | 1097/1692 | 993/1383 | 331/460 | chr1 | 3632268 | |||
| chr1:3633436 | C | T | 1 | a0008 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.884G>A | p.Arg295Gln | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/12 | 988/1692 | 884/1383 | 295/460 | chr1 | 3633436 | |||
| chr1:3635173 | C | T | 1 | a0007 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.725G>A | p.Ser242Asn | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 7/12 | 829/1692 | 725/1383 | 242/460 | chr1 | 3635173 | |||
| chr1:3635219 | T | C | 1 | a0006 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.679A>G | p.Lys227Glu | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 7/12 | 783/1692 | 679/1383 | 227/460 | chr1 | 3635219 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:3631038 | G | A | 1 | a0001c0013 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.1320C>T | p.Leu440Leu | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 12/12 | 1424/1692 | 1320/1383 | 440/460 | chr1 | 3631038 | |||
| chr1:3631071 | C | T | 1 | a0004c0007 | 3 | HG02723.hp1 HG03098.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1287G>A | p.Ser429Ser | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 12/12 | 1391/1692 | 1287/1383 | 429/460 | chr1 | 3631071 | |||
| chr1:3631572 | T | C | 12 | a0001c0001 a0001c0002 a0001c0006 others(9): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
synonymous_variant | LOW | c.1134A>G | p.Ala378Ala | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 11/12 | 1238/1692 | 1134/1383 | 378/460 | chr1 | 3631572 | |||
| chr1:3633435 | C | G | 1 | a0001c0006 | 5 | HG02818.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
synonymous_variant | LOW | c.885G>C | p.Arg295Arg | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/12 | 989/1692 | 885/1383 | 295/460 | chr1 | 3633435 | |||
| chr1:3635228 | G | A | 2 | a0001c0002 a0006c0014 |
42 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
synonymous_variant | LOW | c.670C>T | p.Leu224Leu | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 7/12 | 774/1692 | 670/1383 | 224/460 | chr1 | 3635228 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:3630951 | T | G | 1 | a0001c0003t0006 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 12/12 | 24 | chr1 | 3630951 | ||||||
| chr1:3630970 | C | T | 1 | a0001c0001t0003 | 2 | HG02258.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 12/12 | 5 | chr1 | 3630970 | ||||||
| chr1:3650007 | G | A | 1 | a0003c0005t0007 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/12 | 8 | chr1 | 3650007 | ||||||
| chr1:3650047 | A | T | 1 | a0001c0001t0009 | 1 | HG00733.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48T>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/12 | 48 | chr1 | 3650047 | ||||||
| chr1:3650060 | C | A | 1 | a0001c0001t0008 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/12 | 61 | chr1 | 3650060 | ||||||
| chr1:3650061 | AGCAGGCT others(1): Show |
A | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(3): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
5_prime_UTR_variant | MODIFIER | c.-70_-63delCAGCCTGC | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/12 | 63 | chr1 | 3650061 | ||||||
| chr1:3650067 | C | A | 1 | a0001c0003t0001 | 1 | HG01175.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/12 | 68 | chr1 | 3650067 | ||||||
| chr1:3650067 | C | T | 1 | a0008c0011t0001 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-68G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/12 | 68 | chr1 | 3650067 | ||||||
| chr1:3650080 | C | T | 1 | a0001c0001t0005 | 1 | HG02630.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/12 | 81 | chr1 | 3650080 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:3631205 | A | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0054 others(17): Show |
33 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1241-88T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 11/11 | chr1 | 3631205 | |||||||
| chr1:3631303 | C | T | 1 | a0001c0001t0003g0022 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1240+163G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 11/11 | chr1 | 3631303 | |||||||
| chr1:3631342 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1240+124G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 11/11 | chr1 | 3631342 | |||||||
| chr1:3631405 | G | A | 3 | a0001c0002t0001g0068 a0001c0002t0001g0128 a0001c0002t0001g0132 |
3 | HG01934.hp1 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1240+61C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 11/11 | chr1 | 3631405 | |||||||
| chr1:3631778 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(39): Show |
95 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1049-121C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3631778 | |||||||
| chr1:3631848 | G | A | 1 | a0001c0001t0003g0022 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1049-191C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3631848 | |||||||
| chr1:3631882 | G | GGT | 8 | a0003c0005t0001g0014 a0003c0005t0001g0021 a0003c0005t0001g0049 others(5): Show |
11 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1049-227_1049-226d others(4): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3631882 | |||||||
| chr1:3631884 | T | TG | 21 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0025 others(18): Show |
36 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1049-228_1049-227i others(3): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3631884 | |||||||
| chr1:3631884 | TA | T | 4 | a0001c0001t0001g0090 a0001c0001t0002g0153 a0001c0002t0001g0137 others(1): Show |
4 | HG01070.hp1 HG03041.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-228delT | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3631884 | |||||||
| chr1:3631885 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1049-228T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3631885 | |||||||
| chr1:3631885 | A | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0025 others(26): Show |
47 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1049-228T>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3631885 | |||||||
| chr1:3631886 | T | G | 4 | a0001c0001t0001g0090 a0001c0001t0002g0153 a0001c0002t0001g0137 others(1): Show |
4 | HG01070.hp1 HG03041.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-229A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3631886 | |||||||
| chr1:3631978 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
182 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1048+235A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3631978 | |||||||
| chr1:3632011 | T | A | 1 | a0001c0001t0002g0154 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1048+202A>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3632011 | |||||||
| chr1:3632109 | C | T | 1 | a0001c0006t0001g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1048+104G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 10/11 | chr1 | 3632109 | |||||||
| chr1:3632380 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.923-42C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632380 | |||||||
| chr1:3632397 | C | CT | 3 | a0001c0003t0001g0023 a0001c0003t0001g0059 a0001c0003t0001g0062 |
4 | HG01123.hp2 HG02615.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.923-60dupA | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632397 | |||||||
| chr1:3632466 | G | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0055 others(17): Show |
32 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.923-128C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632466 | |||||||
| chr1:3632529 | GC | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0054 others(17): Show |
33 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.923-192delG | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632529 | |||||||
| chr1:3632577 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.923-239C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632577 | |||||||
| chr1:3632633 | G | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0054 others(17): Show |
33 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.923-295C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632633 | |||||||
| chr1:3632712 | G | A | 8 | a0003c0005t0001g0014 a0003c0005t0001g0021 a0003c0005t0001g0049 others(5): Show |
11 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.923-374C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632712 | |||||||
| chr1:3632803 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.923-465T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632803 | |||||||
| chr1:3632877 | G | A | 1 | a0001c0001t0004g0038 | 2 | NA19011.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.922+521C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632877 | |||||||
| chr1:3632917 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.922+481T>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632917 | |||||||
| chr1:3632969 | G | A | 3 | a0001c0001t0001g0076 a0001c0001t0002g0155 a0001c0001t0002g0156 |
3 | HG00558.hp1 NA18977.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.922+429C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3632969 | |||||||
| chr1:3633015 | A | C | 8 | a0003c0005t0001g0014 a0003c0005t0001g0021 a0003c0005t0001g0049 others(5): Show |
11 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.922+383T>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3633015 | |||||||
| chr1:3633024 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.922+374C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3633024 | |||||||
| chr1:3633061 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.922+337C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3633061 | |||||||
| chr1:3633107 | TGAAAAAC others(18): Show |
T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0120 a0001c0003t0001g0118 others(1): Show |
8 | HG01261.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.922+266_922+290del others(25): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3633107 | |||||||
| chr1:3633220 | T | G | 1 | a0002c0004t0001g0088 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.922+178A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3633220 | |||||||
| chr1:3633288 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
181 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.922+110C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3633288 | |||||||
| chr1:3633297 | A | G | 1 | a0001c0003t0001g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.922+101T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 9/11 | chr1 | 3633297 | |||||||
| chr1:3633882 | G | C | 1 | a0002c0004t0001g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.817-379C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3633882 | |||||||
| chr1:3634027 | T | C | 1 | a0001c0003t0001g0062 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.817-524A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634027 | |||||||
| chr1:3634037 | TGTGGC | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0121 |
9 | HG00642.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-539_817-535del others(5): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634037 | |||||||
| chr1:3634126 | A | G | 43 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0028 others(40): Show |
81 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.817-623T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634126 | |||||||
| chr1:3634256 | C | G | 1 | a0001c0001t0002g0035 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.816+741G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634256 | |||||||
| chr1:3634257 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.816+740G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634257 | |||||||
| chr1:3634280 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.816+717C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634280 | |||||||
| chr1:3634476 | C | T | 1 | a0008c0011t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.816+521G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634476 | |||||||
| chr1:3634512 | G | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0133 |
3 | NA18986.hp2 NA19056.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.816+485C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634512 | |||||||
| chr1:3634589 | G | A | 1 | a0001c0003t0001g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.816+408C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634589 | |||||||
| chr1:3634595 | T | C | 2 | a0001c0001t0001g0079 a0001c0003t0001g0065 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.816+402A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634595 | |||||||
| chr1:3634660 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.816+337C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634660 | |||||||
| chr1:3634744 | A | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0028 others(20): Show |
38 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.816+253T>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634744 | |||||||
| chr1:3634879 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.816+118C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634879 | |||||||
| chr1:3634942 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.816+55A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 8/11 | chr1 | 3634942 | |||||||
| chr1:3635097 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0054 others(4): Show |
14 | HG00642.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.739-23C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 7/11 | chr1 | 3635097 | |||||||
| chr1:3635334 | C | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0054 others(16): Show |
31 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.604-40G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 6/11 | chr1 | 3635334 | |||||||
| chr1:3635337 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0054 others(16): Show |
31 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.604-43G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 6/11 | chr1 | 3635337 | |||||||
| chr1:3635341 | A | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0054 others(17): Show |
33 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.604-47T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 6/11 | chr1 | 3635341 | |||||||
| chr1:3635678 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.603+266C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 6/11 | chr1 | 3635678 | |||||||
| chr1:3635897 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.603+47G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 6/11 | chr1 | 3635897 | |||||||
| chr1:3636042 | AG | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0001g0121 |
9 | HG00642.hp1 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.517-13delC | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636042 | |||||||
| chr1:3636043 | G | A | 6 | a0001c0001t0002g0001 a0001c0001t0002g0149 a0001c0001t0002g0154 others(3): Show |
13 | NA18943.hp2 NA18954.hp1 NA18959.hp2 others(10): Show |
intron_variant | MODIFIER | c.517-13C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636043 | |||||||
| chr1:3636049 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.517-19C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636049 | |||||||
| chr1:3636052 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.517-22T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636052 | |||||||
| chr1:3636216 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.517-186T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636216 | |||||||
| chr1:3636245 | AAGGGCGG others(70): Show |
A | 1 | a0001c0001t0002g0157 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.517-292_517-216del others(77): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636245 | |||||||
| chr1:3636265 | G | A | 3 | a0001c0006t0001g0015 a0001c0006t0001g0056 a0001c0006t0001g0057 |
5 | HG02818.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-235C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636265 | |||||||
| chr1:3636415 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.517-385G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636415 | |||||||
| chr1:3636462 | C | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(6): Show |
20 | HG00642.hp1 HG01884.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.517-432G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636462 | |||||||
| chr1:3636549 | T | C | 1 | a0001c0003t0001g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.516+446A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636549 | |||||||
| chr1:3636609 | G | A | 1 | a0001c0001t0003g0022 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.516+386C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636609 | |||||||
| chr1:3636649 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.516+346C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636649 | |||||||
| chr1:3636708 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0002g0039 |
4 | HG02080.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+287C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636708 | |||||||
| chr1:3636791 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+204C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636791 | |||||||
| chr1:3636885 | A | T | 1 | a0001c0001t0002g0034 | 2 | NA18977.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.516+110T>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 5/11 | chr1 | 3636885 | |||||||
| chr1:3637225 | T | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.413-127A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637225 | |||||||
| chr1:3637264 | C | T | 16 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0091 others(13): Show |
23 | HG01109.hp2 HG01255.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.413-166G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637264 | |||||||
| chr1:3637291 | C | G | 15 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0122 others(12): Show |
22 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.413-193G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637291 | |||||||
| chr1:3637425 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.413-327G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637425 | |||||||
| chr1:3637429 | T | TC | 34 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
78 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.413-332dupG | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637429 | |||||||
| chr1:3637472 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.413-374G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637472 | |||||||
| chr1:3637498 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.413-400G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637498 | |||||||
| chr1:3637519 | T | G | 1 | a0001c0002t0001g0130 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.413-421A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637519 | |||||||
| chr1:3637671 | A | G | 16 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(13): Show |
23 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.413-573T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637671 | |||||||
| chr1:3637817 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-719C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637817 | |||||||
| chr1:3637834 | A | T | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.413-736T>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637834 | |||||||
| chr1:3637948 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.412+802C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3637948 | |||||||
| chr1:3638025 | G | A | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.412+725C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638025 | |||||||
| chr1:3638048 | A | G | 1 | a0001c0001t0002g0020 | 3 | NA18941.hp2 NA18964.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.412+702T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638048 | |||||||
| chr1:3638060 | G | A | 28 | a0001c0001t0001g0025 a0001c0001t0001g0069 a0001c0001t0001g0070 others(25): Show |
39 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.412+690C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638060 | |||||||
| chr1:3638088 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(5): Show |
19 | HG00642.hp1 HG02109.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.412+662G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638088 | |||||||
| chr1:3638204 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(4): Show |
15 | HG00741.hp1 HG01167.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.412+546C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638204 | |||||||
| chr1:3638205 | C | T | 1 | a0002c0004t0001g0030 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.412+545G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638205 | |||||||
| chr1:3638372 | GAA | G | 8 | a0003c0005t0001g0014 a0003c0005t0001g0021 a0003c0005t0001g0049 others(5): Show |
11 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+376_412+377del others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638372 | |||||||
| chr1:3638424 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(29): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.412+326G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638424 | |||||||
| chr1:3638425 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(5): Show |
19 | HG00642.hp1 HG02109.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.412+325C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638425 | |||||||
| chr1:3638445 | C | A | 1 | a0001c0001t0002g0159 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.412+305G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638445 | |||||||
| chr1:3638484 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.412+266C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638484 | |||||||
| chr1:3638527 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+223A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 4/11 | chr1 | 3638527 | |||||||
| chr1:3638859 | C | A | 1 | a0001c0001t0002g0040 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.340-37G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3638859 | |||||||
| chr1:3638864 | G | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.340-42C>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3638864 | |||||||
| chr1:3638898 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-76G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3638898 | |||||||
| chr1:3638902 | G | A | 3 | a0001c0002t0001g0135 a0003c0005t0001g0051 a0003c0005t0001g0052 |
3 | HG00621.hp1 HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.340-80C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3638902 | |||||||
| chr1:3638906 | C | T | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-84G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3638906 | |||||||
| chr1:3638978 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0080 |
3 | HG03579.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.340-156A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3638978 | |||||||
| chr1:3639029 | CTGT | C | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-210_340-208del others(3): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639029 | |||||||
| chr1:3639089 | A | G | 1 | a0003c0005t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.340-267T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639089 | |||||||
| chr1:3639108 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.340-286G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639108 | |||||||
| chr1:3639111 | T | C | 2 | a0001c0003t0001g0071 a0001c0003t0001g0072 |
2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.340-289A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639111 | |||||||
| chr1:3639306 | T | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.340-484A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639306 | |||||||
| chr1:3639322 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.340-500C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639322 | |||||||
| chr1:3639376 | GACTGTCC | G | 2 | a0001c0003t0001g0024 a0001c0003t0001g0063 |
3 | HG01261.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.340-561_340-555del others(7): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639376 | |||||||
| chr1:3639434 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.340-612C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639434 | |||||||
| chr1:3639480 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.340-658C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639480 | |||||||
| chr1:3639503 | G | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0018 others(5): Show |
20 | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.340-681C>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639503 | |||||||
| chr1:3639534 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0003t0001g0061 others(1): Show |
7 | HG01123.hp2 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-712G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639534 | |||||||
| chr1:3639671 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.340-849C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639671 | |||||||
| chr1:3639689 | G | GTGCGGGG others(53): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-927_340-868dup others(60): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639689 | |||||||
| chr1:3639692 | C | CGGGGTGG others(53): Show |
4 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG02735.hp1 HG03516.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-930_340-871dup others(60): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639692 | |||||||
| chr1:3639692 | C | CGGGGTGG others(113): Show |
2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01255.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.340-871_340-870ins others(120): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639692 | |||||||
| chr1:3639692 | CGGGGTGG others(53): Show |
C | 4 | a0001c0006t0001g0015 a0001c0006t0001g0056 a0001c0006t0001g0057 others(1): Show |
6 | HG02818.hp1 HG02922.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-930_340-871del others(60): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639692 | |||||||
| chr1:3639752 | T | TGGGGTGG others(53): Show |
1 | a0002c0004t0001g0003 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.340-990_340-931dup others(60): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639752 | |||||||
| chr1:3639791 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.340-969T>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639791 | |||||||
| chr1:3639812 | C | T | 1 | a0001c0013t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.340-990G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639812 | |||||||
| chr1:3639819 | G | A | 1 | a0001c0001t0002g0041 | 2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.340-997C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639819 | |||||||
| chr1:3639881 | G | A | 3 | a0001c0003t0001g0024 a0001c0003t0001g0067 a0001c0003t0001g0124 |
4 | HG00280.hp2 HG00738.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-1059C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639881 | |||||||
| chr1:3639892 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.340-1070A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639892 | |||||||
| chr1:3639996 | T | G | 1 | a0001c0003t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340-1174A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3639996 | |||||||
| chr1:3640093 | G | A | 1 | a0001c0006t0001g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.340-1271C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640093 | |||||||
| chr1:3640112 | G | T | 1 | a0001c0001t0001g0136 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.340-1290C>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640112 | |||||||
| chr1:3640282 | G | C | 1 | a0001c0001t0002g0161 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.340-1460C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640282 | |||||||
| chr1:3640291 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.340-1469G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640291 | |||||||
| chr1:3640302 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.340-1480C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640302 | |||||||
| chr1:3640323 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.340-1501A>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640323 | |||||||
| chr1:3640326 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0106 |
4 | HG02135.hp1 NA18612.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-1504C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640326 | |||||||
| chr1:3640342 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.340-1520T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640342 | |||||||
| chr1:3640395 | C | G | 2 | a0001c0002t0001g0032 a0001c0002t0001g0133 |
3 | NA18986.hp2 NA19056.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.340-1573G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640395 | |||||||
| chr1:3640400 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-1578G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640400 | |||||||
| chr1:3640425 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.340-1603C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640425 | |||||||
| chr1:3640451 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.340-1629G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640451 | |||||||
| chr1:3640475 | AGGGTGGA others(141): Show |
A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(4): Show |
15 | HG00741.hp1 HG01167.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.340-1801_340-1654d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640475 | |||||||
| chr1:3640477 | GGTGGAAC others(41): Show |
G | 1 | a0001c0003t0001g0066 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.340-1703_340-1656d others(50): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640477 | |||||||
| chr1:3640485 | ACCCGAGG others(30): Show |
A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(136): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.340-1700_340-1664d others(39): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640485 | |||||||
| chr1:3640489 | GAGGCTCT others(104): Show |
G | 2 | a0001c0003t0001g0023 a0001c0003t0001g0059 |
3 | HG02615.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.340-1778_340-1668d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640489 | |||||||
| chr1:3640518 | CAGCGCCC others(104): Show |
C | 1 | a0001c0002t0001g0004 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.340-1807_340-1697d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640518 | |||||||
| chr1:3640538 | ATCAGCAG others(67): Show |
A | 3 | a0001c0001t0002g0148 a0001c0001t0002g0163 a0001c0001t0008g0140 |
3 | HG00735.hp2 HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.340-1790_340-1717d others(76): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640538 | |||||||
| chr1:3640547 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(3): Show |
17 | HG00642.hp1 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.340-1725C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640547 | |||||||
| chr1:3640549 | G | A | 14 | a0001c0001t0001g0055 a0001c0001t0002g0001 a0001c0001t0002g0013 others(11): Show |
22 | HG00735.hp1 HG01069.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-1727C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640549 | |||||||
| chr1:3640555 | C | G | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-1733G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640555 | |||||||
| chr1:3640557 | G | A | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-1735C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640557 | |||||||
| chr1:3640563 | G | C | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-1741C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640563 | |||||||
| chr1:3640575 | A | G | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-1753T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640575 | |||||||
| chr1:3640586 | A | G | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-1764T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640586 | |||||||
| chr1:3640594 | A | G | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-1772T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640594 | |||||||
| chr1:3640600 | C | G | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-1778G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640600 | |||||||
| chr1:3640612 | G | A | 12 | a0001c0001t0001g0055 a0001c0006t0001g0015 a0001c0006t0001g0056 others(9): Show |
17 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.340-1790C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640612 | |||||||
| chr1:3640623 | G | A | 15 | a0001c0001t0001g0055 a0001c0001t0002g0148 a0001c0001t0002g0163 others(12): Show |
20 | HG00735.hp2 HG01109.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.340-1801C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640623 | |||||||
| chr1:3640631 | G | A | 3 | a0001c0001t0002g0148 a0001c0001t0002g0163 a0001c0001t0008g0140 |
3 | HG00735.hp2 HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.340-1809C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640631 | |||||||
| chr1:3640636 | C | G | 1 | a0001c0003t0001g0059 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.340-1814G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640636 | |||||||
| chr1:3640637 | G | C | 3 | a0001c0001t0002g0148 a0001c0001t0002g0163 a0001c0001t0008g0140 |
3 | HG00735.hp2 HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.340-1815C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640637 | |||||||
| chr1:3640640 | G | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-1818C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640640 | |||||||
| chr1:3640641 | C | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-1819G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640641 | |||||||
| chr1:3640645 | G | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-1823C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640645 | |||||||
| chr1:3640649 | A | G | 3 | a0001c0001t0002g0148 a0001c0001t0002g0163 a0001c0001t0008g0140 |
3 | HG00735.hp2 HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.340-1827T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640649 | |||||||
| chr1:3640666 | G | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-1844C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640666 | |||||||
| chr1:3640670 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-1848C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640670 | |||||||
| chr1:3640671 | C | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-1849G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640671 | |||||||
| chr1:3640696 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.340-1874G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640696 | |||||||
| chr1:3640734 | G | A | 12 | a0001c0002t0001g0004 a0001c0002t0001g0032 a0001c0002t0001g0068 others(9): Show |
23 | HG00609.hp2 HG01934.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.340-1912C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3640734 | |||||||
| chr1:3641123 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0085 |
8 | HG00642.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-2301C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641123 | |||||||
| chr1:3641129 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-2307G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641129 | |||||||
| chr1:3641254 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-2432C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641254 | |||||||
| chr1:3641317 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-2495G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641317 | |||||||
| chr1:3641358 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0090 |
4 | HG00738.hp2 HG01106.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-2536G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641358 | |||||||
| chr1:3641498 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(3): Show |
17 | HG00642.hp1 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.340-2676G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641498 | |||||||
| chr1:3641557 | C | G | 27 | a0001c0001t0001g0025 a0001c0001t0001g0069 a0001c0001t0001g0070 others(24): Show |
38 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.340-2735G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641557 | |||||||
| chr1:3641567 | C | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
39 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.340-2745G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641567 | |||||||
| chr1:3641573 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.340-2751G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641573 | |||||||
| chr1:3641581 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.340-2759G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641581 | |||||||
| chr1:3641609 | C | CA | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-2788dupT | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641609 | |||||||
| chr1:3641624 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.340-2802C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641624 | |||||||
| chr1:3641631 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-2809C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641631 | |||||||
| chr1:3641664 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-2842G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641664 | |||||||
| chr1:3641669 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.340-2847T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641669 | |||||||
| chr1:3641698 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.340-2876C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641698 | |||||||
| chr1:3641761 | GAAAA | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(4): Show |
15 | HG00741.hp1 HG01167.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.340-2943_340-2940d others(6): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641761 | |||||||
| chr1:3641769 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(8): Show |
21 | HG00741.hp1 HG01167.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.340-2947G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641769 | |||||||
| chr1:3641913 | G | A | 1 | a0001c0002t0001g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.340-3091C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641913 | |||||||
| chr1:3641919 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.340-3097C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3641919 | |||||||
| chr1:3642000 | C | T | 3 | a0001c0006t0001g0015 a0001c0006t0001g0056 a0001c0006t0001g0057 |
5 | HG02818.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-3178G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642000 | |||||||
| chr1:3642168 | G | T | 1 | a0001c0002t0001g0126 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.340-3346C>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642168 | |||||||
| chr1:3642169 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.340-3347G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642169 | |||||||
| chr1:3642215 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.340-3393G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642215 | |||||||
| chr1:3642224 | C | T | 1 | a0001c0002t0001g0033 | 2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.340-3402G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642224 | |||||||
| chr1:3642266 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
7 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.340-3444T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642266 | |||||||
| chr1:3642306 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.340-3484A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642306 | |||||||
| chr1:3642393 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0080 |
3 | HG03579.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.340-3571C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642393 | |||||||
| chr1:3642449 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.340-3627G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642449 | |||||||
| chr1:3642466 | C | T | 17 | a0001c0002t0001g0068 a0001c0003t0001g0011 a0001c0003t0001g0012 others(14): Show |
25 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.340-3644G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642466 | |||||||
| chr1:3642606 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.340-3784C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642606 | |||||||
| chr1:3642662 | G | T | 2 | a0001c0003t0001g0118 a0001c0003t0006g0119 |
2 | HG01261.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.340-3840C>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642662 | |||||||
| chr1:3642737 | C | CA | 11 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0083 others(8): Show |
12 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-3916dupT | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642737 | |||||||
| chr1:3642737 | CA | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(61): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.340-3916delT | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642737 | |||||||
| chr1:3642737 | CAA | C | 9 | a0001c0001t0001g0048 a0001c0001t0001g0075 a0001c0001t0001g0085 others(6): Show |
12 | HG00621.hp2 HG01167.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.340-3917_340-3916d others(4): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642737 | |||||||
| chr1:3642918 | A | G | 19 | a0001c0001t0001g0136 a0001c0002t0001g0004 a0001c0002t0001g0005 others(16): Show |
42 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.339+3748T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642918 | |||||||
| chr1:3642996 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.339+3670C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3642996 | |||||||
| chr1:3643107 | A | C | 1 | a0009c0012t0001g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.339+3559T>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643107 | |||||||
| chr1:3643141 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.339+3525C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643141 | |||||||
| chr1:3643179 | A | C | 1 | a0001c0001t0001g0029 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.339+3487T>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643179 | |||||||
| chr1:3643337 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(3): Show |
17 | HG00642.hp1 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.339+3329C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643337 | |||||||
| chr1:3643366 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
7 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+3300C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643366 | |||||||
| chr1:3643459 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
7 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+3207G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643459 | |||||||
| chr1:3643460 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.339+3206C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643460 | |||||||
| chr1:3643554 | TCAGCGGC others(43): Show |
T | 2 | a0001c0002t0001g0125 a0001c0002t0001g0135 |
2 | HG00621.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.339+3062_339+3111d others(52): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643554 | |||||||
| chr1:3643565 | A | G | 17 | a0001c0001t0001g0136 a0001c0002t0001g0004 a0001c0002t0001g0005 others(14): Show |
40 | HG00323.hp1 HG00609.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.339+3101T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643565 | |||||||
| chr1:3643567 | T | TG | 14 | a0001c0001t0001g0136 a0001c0002t0001g0004 a0001c0002t0001g0005 others(11): Show |
32 | HG00323.hp1 HG00609.hp2 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.339+3098_339+3099i others(3): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643567 | |||||||
| chr1:3643567 | T | TGAGCCCC others(45): Show |
2 | a0001c0002t0001g0009 a0001c0002t0001g0033 |
5 | HG01496.hp2 HG02055.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+3098_339+3099i others(54): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643567 | |||||||
| chr1:3643567 | T | TGAGCCCC others(96): Show |
1 | a0001c0002t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.339+3098_339+3099i others(105): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643567 | |||||||
| chr1:3643567 | T | TGAGCCCC others(198): Show |
1 | a0001c0002t0001g0009 | 2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.339+3098_339+3099i others(207): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643567 | |||||||
| chr1:3643569 | A | G | 17 | a0001c0001t0001g0136 a0001c0002t0001g0004 a0001c0002t0001g0005 others(14): Show |
40 | HG00323.hp1 HG00609.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.339+3097T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643569 | |||||||
| chr1:3643574 | C | G | 17 | a0001c0001t0001g0136 a0001c0002t0001g0004 a0001c0002t0001g0005 others(14): Show |
40 | HG00323.hp1 HG00609.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.339+3092G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643574 | |||||||
| chr1:3643574 | C | T | 2 | a0001c0003t0001g0071 a0001c0003t0001g0072 |
2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.339+3092G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643574 | |||||||
| chr1:3643577 | A | AATGGGGT others(95): Show |
2 | a0001c0001t0002g0170 a0001c0001t0003g0022 |
3 | HG02258.hp2 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.339+2987_339+3088d others(104): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | A | AATGGGGT others(146): Show |
1 | a0001c0001t0001g0008 | 5 | HG02109.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+2936_339+3088d others(155): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | A | AATGGGGT others(248): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0080 |
3 | HG03579.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.339+2834_339+3088d others(257): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | A | C | 17 | a0001c0001t0001g0136 a0001c0002t0001g0004 a0001c0002t0001g0005 others(14): Show |
40 | HG00323.hp1 HG00609.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.339+3089T>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | AATGGGGT others(44): Show |
A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0085 a0001c0001t0002g0001 others(1): Show |
10 | HG00642.hp1 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.339+3038_339+3088d others(53): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | AATGGGGT others(95): Show |
A | 2 | a0001c0001t0001g0054 a0001c0001t0002g0001 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.339+2987_339+3088d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | AATGGGGT others(146): Show |
A | 44 | a0001c0001t0001g0029 a0001c0001t0001g0075 a0001c0001t0001g0076 others(41): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.339+2936_339+3088d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | AATGGGGT others(197): Show |
A | 5 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0143 others(2): Show |
8 | HG00735.hp1 HG01069.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.339+2885_339+3088d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | AATGGGGT others(248): Show |
A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0013 |
3 | HG00639.hp2 HG01123.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.339+2834_339+3088d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | AATGGGGT others(350): Show |
A | 1 | a0001c0001t0002g0040 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.339+2732_339+3088d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643577 | AATGGGGT others(401): Show |
A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
7 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+2681_339+3088d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643577 | |||||||
| chr1:3643586 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.339+3080C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643586 | |||||||
| chr1:3643660 | G | A | 1 | a0001c0006t0001g0015 | 3 | HG03195.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.339+3006C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643660 | |||||||
| chr1:3643680 | A | G | 9 | a0001c0001t0001g0047 a0003c0005t0001g0014 a0003c0005t0001g0021 others(6): Show |
12 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.339+2986T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643680 | |||||||
| chr1:3643719 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.339+2947A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643719 | |||||||
| chr1:3643731 | A | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(12): Show |
26 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+2935T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643731 | |||||||
| chr1:3643773 | GCCCCGGA others(145): Show |
G | 1 | a0001c0001t0002g0145 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.339+2741_339+2892d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643773 | |||||||
| chr1:3643782 | A | G | 10 | a0001c0001t0001g0044 a0001c0001t0001g0055 a0003c0005t0001g0014 others(7): Show |
13 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.339+2884T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643782 | |||||||
| chr1:3643807 | C | T | 1 | a0003c0005t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.339+2859G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643807 | |||||||
| chr1:3643812 | CGGCCCCG others(554): Show |
C | 1 | a0002c0004t0001g0003 | 9 | HG00642.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.339+2293_339+2853d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643812 | |||||||
| chr1:3643833 | A | G | 9 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0003c0005t0001g0014 others(6): Show |
12 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+2833T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643833 | |||||||
| chr1:3643842 | C | T | 1 | a0002c0004t0001g0003 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.339+2824G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643842 | |||||||
| chr1:3643860 | CAGCGGCC others(554): Show |
C | 1 | a0003c0005t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.339+2245_339+2805d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643860 | |||||||
| chr1:3643863 | CGGCCCCG others(503): Show |
C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.339+2293_339+2802d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643863 | |||||||
| chr1:3643884 | A | G | 7 | a0003c0005t0001g0014 a0003c0005t0001g0021 a0003c0005t0001g0051 others(4): Show |
10 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.339+2782T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643884 | |||||||
| chr1:3643909 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(11): Show |
25 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.339+2757G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643909 | |||||||
| chr1:3643935 | A | G | 5 | a0003c0005t0001g0014 a0003c0005t0001g0051 a0003c0005t0001g0052 others(2): Show |
7 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+2731T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643935 | |||||||
| chr1:3643942 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.339+2724G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643942 | |||||||
| chr1:3643962 | CAGCGGCC others(452): Show |
C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(11): Show |
25 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.339+2245_339+2703d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643962 | |||||||
| chr1:3643965 | C | T | 1 | a0009c0012t0001g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.339+2701G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643965 | |||||||
| chr1:3643987 | T | C | 1 | a0001c0001t0002g0162 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.339+2679A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3643987 | |||||||
| chr1:3644011 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.339+2655G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644011 | |||||||
| chr1:3644016 | CGGCCCCG others(350): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.339+2293_339+2649d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644016 | |||||||
| chr1:3644030 | C | T | 1 | a0001c0003t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.339+2636G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644030 | |||||||
| chr1:3644047 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.339+2619C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644047 | |||||||
| chr1:3644062 | C | T | 3 | a0001c0006t0001g0015 a0001c0006t0001g0056 a0001c0006t0001g0057 |
5 | HG02818.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+2604G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644062 | |||||||
| chr1:3644064 | CAGCGGCC others(350): Show |
C | 1 | a0001c0001t0001g0045 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.339+2245_339+2601d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644064 | |||||||
| chr1:3644115 | CAGCGGCC others(299): Show |
C | 3 | a0001c0006t0001g0015 a0001c0006t0001g0056 a0001c0006t0001g0057 |
5 | HG02818.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+2245_339+2550d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644115 | |||||||
| chr1:3644164 | C | T | 1 | a0004c0008t0001g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.339+2502G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644164 | |||||||
| chr1:3644166 | CAGCGGCC others(248): Show |
C | 1 | a0004c0008t0001g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.339+2245_339+2499d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644166 | |||||||
| chr1:3644215 | C | T | 30 | a0001c0001t0001g0025 a0001c0001t0001g0069 a0001c0001t0001g0070 others(27): Show |
40 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.339+2451G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644215 | |||||||
| chr1:3644217 | CAGCGGCC others(197): Show |
C | 30 | a0001c0001t0001g0025 a0001c0001t0001g0069 a0001c0001t0001g0070 others(27): Show |
40 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.339+2245_339+2448d others(2): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644217 | |||||||
| chr1:3644352 | C | T | 1 | a0001c0001t0002g0001 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.339+2314G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644352 | |||||||
| chr1:3644373 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(3): Show |
17 | HG00642.hp1 HG02109.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.339+2293A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644373 | |||||||
| chr1:3644421 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.339+2245A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644421 | |||||||
| chr1:3644430 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0085 |
8 | HG00642.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.339+2236G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644430 | |||||||
| chr1:3644434 | A | G | 19 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(16): Show |
32 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.339+2232T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644434 | |||||||
| chr1:3644444 | C | T | 78 | a0001c0001t0001g0025 a0001c0001t0001g0069 a0001c0001t0001g0070 others(75): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.339+2222G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644444 | |||||||
| chr1:3644694 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
7 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+1972C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644694 | |||||||
| chr1:3644885 | G | A | 1 | a0001c0003t0001g0073 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.339+1781C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644885 | |||||||
| chr1:3644958 | C | T | 1 | a0001c0003t0001g0058 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.339+1708G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644958 | |||||||
| chr1:3644965 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0048 |
6 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+1701C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3644965 | |||||||
| chr1:3645034 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.339+1632G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645034 | |||||||
| chr1:3645091 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.339+1575C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645091 | |||||||
| chr1:3645341 | AGCGGCGC others(69): Show |
A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.339+1249_339+1324d others(78): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645341 | |||||||
| chr1:3645343 | CGGCGCAG others(31): Show |
C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0112 a0001c0001t0001g0120 others(3): Show |
8 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.339+1285_339+1322d others(40): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645343 | |||||||
| chr1:3645356 | T | C | 10 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0147 others(7): Show |
30 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.339+1310A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645356 | |||||||
| chr1:3645356 | TGGGCGGG others(31): Show |
T | 2 | a0001c0001t0001g0054 a0001c0001t0002g0020 |
4 | HG01884.hp2 NA18941.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+1272_339+1309d others(40): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645356 | |||||||
| chr1:3645381 | TGGCGCAG others(31): Show |
T | 8 | a0003c0005t0001g0014 a0003c0005t0001g0021 a0003c0005t0001g0049 others(5): Show |
11 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.339+1247_339+1284d others(40): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645381 | |||||||
| chr1:3645384 | C | CGCAGCGG others(69): Show |
3 | a0001c0006t0001g0015 a0001c0006t0001g0056 a0001c0006t0001g0057 |
5 | HG02818.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+1206_339+1281d others(78): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645384 | |||||||
| chr1:3645420 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.339+1246C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645420 | |||||||
| chr1:3645422 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.339+1244G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645422 | |||||||
| chr1:3645422 | CGCAGCGG others(31): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.339+1206_339+1243d others(40): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645422 | |||||||
| chr1:3645428 | G | C | 1 | a0001c0001t0001g0002 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.339+1238C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645428 | |||||||
| chr1:3645432 | C | CGGGCGGG others(69): Show |
8 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(5): Show |
16 | HG00741.hp1 HG01167.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.339+1158_339+1233d others(78): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645432 | |||||||
| chr1:3645432 | C | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0018 others(28): Show |
68 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.339+1234G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645432 | |||||||
| chr1:3645432 | CGGGCGGG others(69): Show |
C | 1 | a0001c0001t0002g0039 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.339+1158_339+1233d others(78): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645432 | |||||||
| chr1:3645448 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.339+1218A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645448 | |||||||
| chr1:3645458 | C | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.339+1208G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645458 | |||||||
| chr1:3645460 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.339+1206A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645460 | |||||||
| chr1:3645470 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.339+1196G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645470 | |||||||
| chr1:3645496 | G | A | 1 | a0001c0001t0001g0008 | 5 | HG02109.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+1170C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645496 | |||||||
| chr1:3645508 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.339+1158A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645508 | |||||||
| chr1:3645964 | C | A | 1 | a0001c0002t0001g0138 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.339+702G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645964 | |||||||
| chr1:3645987 | T | G | 1 | a0003c0005t0001g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.339+679A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3645987 | |||||||
| chr1:3646022 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.339+644G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3646022 | |||||||
| chr1:3646133 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.339+533C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3646133 | |||||||
| chr1:3646149 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.339+517T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3646149 | |||||||
| chr1:3646171 | G | A | 2 | a0001c0001t0002g0143 a0001c0001t0002g0171 |
2 | HG01192.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.339+495C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3646171 | |||||||
| chr1:3646303 | G | C | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0004c0007t0001g0027 others(1): Show |
5 | HG02723.hp1 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+363C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3646303 | |||||||
| chr1:3646338 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.339+328A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3646338 | |||||||
| chr1:3646365 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.339+301G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3646365 | |||||||
| chr1:3646392 | T | C | 19 | a0001c0001t0001g0136 a0001c0002t0001g0004 a0001c0002t0001g0005 others(16): Show |
42 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.339+274A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3646392 | |||||||
| chr1:3646594 | C | T | 1 | a0001c0002t0001g0134 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.339+72G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 3/11 | chr1 | 3646594 | |||||||
| chr1:3646864 | C | T | 22 | a0001c0001t0001g0025 a0001c0001t0001g0069 a0001c0001t0001g0070 others(19): Show |
31 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.223-82G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 2/11 | chr1 | 3646864 | |||||||
| chr1:3646876 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.223-94G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 2/11 | chr1 | 3646876 | |||||||
| chr1:3646924 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0080 a0001c0001t0001g0081 |
4 | HG02258.hp1 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-142G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 2/11 | chr1 | 3646924 | |||||||
| chr1:3646948 | GC | G | 76 | a0001c0001t0001g0025 a0001c0001t0001g0069 a0001c0001t0001g0070 others(73): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.223-167delG | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 2/11 | chr1 | 3646948 | |||||||
| chr1:3646950 | A | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(17): Show |
33 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.223-168T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 2/11 | chr1 | 3646950 | |||||||
| chr1:3646962 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.223-180T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 2/11 | chr1 | 3646962 | |||||||
| chr1:3647040 | G | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
7 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-258C>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 2/11 | chr1 | 3647040 | |||||||
| chr1:3647132 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.222+276G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 2/11 | chr1 | 3647132 | |||||||
| chr1:3647225 | A | C | 1 | a0001c0001t0002g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.222+183T>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 2/11 | chr1 | 3647225 | |||||||
| chr1:3647651 | T | C | 1 | a0001c0001t0001g0008 | 5 | HG02109.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-91A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3647651 | |||||||
| chr1:3647667 | C | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(41): Show |
82 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.70-107G>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3647667 | |||||||
| chr1:3647835 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.70-275A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3647835 | |||||||
| chr1:3647846 | T | C | 1 | a0001c0001t0002g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.70-286A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3647846 | |||||||
| chr1:3648100 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.70-540T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3648100 | |||||||
| chr1:3648152 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.70-592C>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3648152 | |||||||
| chr1:3648254 | A | T | 36 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(33): Show |
70 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.70-694T>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3648254 | |||||||
| chr1:3648286 | T | C | 2 | a0002c0004t0001g0115 a0002c0004t0001g0116 |
2 | HG02257.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.70-726A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3648286 | |||||||
| chr1:3648367 | T | C | 1 | a0004c0007t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.70-807A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3648367 | |||||||
| chr1:3648437 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.70-877T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3648437 | |||||||
| chr1:3648607 | T | G | 2 | a0001c0003t0001g0118 a0001c0003t0006g0119 |
2 | HG01261.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.70-1047A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3648607 | |||||||
| chr1:3648626 | C | T | 1 | a0001c0001t0003g0022 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.70-1066G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3648626 | |||||||
| chr1:3648809 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.69+1122A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3648809 | |||||||
| chr1:3649147 | G | C | 1 | a0001c0001t0002g0173 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.69+784C>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649147 | |||||||
| chr1:3649174 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.69+757T>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649174 | |||||||
| chr1:3649252 | C | A | 6 | a0001c0001t0001g0136 a0001c0002t0001g0005 a0001c0002t0001g0134 others(3): Show |
13 | HG00323.hp1 HG00621.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.69+679G>T | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649252 | |||||||
| chr1:3649270 | C | T | 1 | a0001c0001t0001g0008 | 5 | HG02109.hp1 HG02280.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+661G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649270 | |||||||
| chr1:3649281 | GCCATGAG others(16): Show |
G | 1 | a0001c0001t0002g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.69+627_69+649delTA others(21): Show |
WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649281 | |||||||
| chr1:3649511 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
7 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+420A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649511 | |||||||
| chr1:3649715 | C | T | 8 | a0003c0005t0001g0014 a0003c0005t0001g0021 a0003c0005t0001g0049 others(5): Show |
11 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+216G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649715 | |||||||
| chr1:3649722 | G | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0044 others(4): Show |
15 | HG00741.hp1 HG01167.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.69+209C>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649722 | |||||||
| chr1:3649776 | T | C | 1 | a0001c0003t0001g0124 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69+155A>G | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649776 | |||||||
| chr1:3649778 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.69+153G>A | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649778 | |||||||
| chr1:3649869 | T | G | 19 | a0001c0001t0001g0136 a0001c0002t0001g0004 a0001c0002t0001g0005 others(16): Show |
42 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.69+62A>C | WRAP73 | ENSG00000116213.16 | transcript | ENST00000270708.12 | protein_coding | 1/11 | chr1 | 3649869 |