Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7844 |
| ensemblid | ENSG00000239305.7 |
| hgncid | 12859 |
| symbol | RNF103 |
| name | ring finger protein 103 |
| refseq_nuc | NM_005667.4 |
| refseq_prot | NP_005658.1 |
| ensembl_nuc | ENST00000237455.5 |
| ensembl_prot | ENSP00000237455.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 86603398 |
| end | 86623865 |
| strand | - |
| ver | v1.2 |
| region | chr2:86603398-86623865 |
| region5000 | chr2:86598398-86628865 |
| regionname0 | RNF103_chr2_86603398_86623865 |
| regionname5000 | RNF103_chr2_86598398_86628865 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 685 | 392 | 92 | 68 | 175 | 16 | 39 | 136 | RNF103_chr2_86598398_86628865 | RNF103 | MWLKL others(680): Show |
chr2 | 86598398 | 86628865 |
| a0002 | 0/0 | 685 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | MWLKL others(680): Show |
chr2 | 86598398 | 86628865 |
| a0003 | 0/0 | 685 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | MWLKL others(680): Show |
chr2 | 86598398 | 86628865 |
| a0004 | 0/0 | 685 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | MWLKL others(680): Show |
chr2 | 86598398 | 86628865 |
| a0005 | 0/0 | 685 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | MWLKL others(680): Show |
chr2 | 86598398 | 86628865 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2055 | 363 | 65 | 67 | 174 | 16 | 39 | RNF103_chr2_86598398_86628865 | RNF103 | ATGTG others(2050): Show |
chr2 | 86598398 | 86628865 | ||
| a0001c0002 | 0/0 | 2055 | 27 | 27 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | ATGTG others(2050): Show |
chr2 | 86598398 | 86628865 | ||
| a0001c0006 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | ATGTG others(2050): Show |
chr2 | 86598398 | 86628865 | ||
| a0001c0008 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | ATGTG others(2050): Show |
chr2 | 86598398 | 86628865 | ||
| a0002c0003 | 0/0 | 2055 | 5 | 0 | 0 | 0 | 0 | 5 | RNF103_chr2_86598398_86628865 | RNF103 | ATGTG others(2050): Show |
chr2 | 86598398 | 86628865 | ||
| a0003c0004 | 0/0 | 2055 | 3 | 0 | 3 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | ATGTG others(2050): Show |
chr2 | 86598398 | 86628865 | ||
| a0004c0007 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | ATGTG others(2050): Show |
chr2 | 86598398 | 86628865 | ||
| a0005c0005 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | ATGTG others(2050): Show |
chr2 | 86598398 | 86628865 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3482 | 254 | 29 | 39 | 149 | 9 | 28 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0002 | 1/1 | 3482 | 70 | 18 | 21 | 14 | 5 | 10 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0003 | 0/0 | 3482 | 16 | 5 | 3 | 6 | 2 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0004 | 0/0 | 3482 | 7 | 7 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0005 | 0/0 | 3482 | 6 | 4 | 2 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0007 | 0/0 | 3482 | 4 | 0 | 0 | 4 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0008 | 0/0 | 3482 | 2 | 0 | 2 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0010 | 0/0 | 3482 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0011 | 0/0 | 3482 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0013 | 0/0 | 3482 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0001t0014 | 0/0 | 3482 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0002t0001 | 0/0 | 3482 | 19 | 19 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0002t0002 | 0/0 | 3482 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0002t0006 | 0/0 | 3482 | 5 | 5 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0002t0009 | 0/0 | 3482 | 2 | 2 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0006t0001 | 0/0 | 3482 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0001c0008t0001 | 0/0 | 3482 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0002c0003t0002 | 0/0 | 3482 | 4 | 0 | 0 | 0 | 0 | 4 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0002c0003t0012 | 0/0 | 3482 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0003c0004t0001 | 0/0 | 3482 | 3 | 0 | 3 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0004c0007t0001 | 0/0 | 3482 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| a0005c0005t0001 | 0/0 | 3482 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | GTTAT others(3477): Show |
chr2 | 86598398 | 86628865 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 61 | 0 | 5 | 44 | 0 | 12 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0026 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0027 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0032 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0034 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0003 | 0/0 | 11 | 1 | 3 | 2 | 3 | 2 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0005 | 0/0 | 8 | 4 | 2 | 0 | 2 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0047 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0017 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0004g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0005g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0005g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0007g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0008g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0001t0014g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0006g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0002t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0006t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0001c0008t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0002c0003t0002g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0002c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0002c0003t0012g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0003c0004t0001g0033 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0004c0007t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| a0005c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01069 | hp2 | a0003 | c0004 | t0001 | g0033 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01071 | hp1 | a0003 | c0004 | t0001 | g0033 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01081 | hp1 | a0003 | c0004 | t0001 | g0033 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01099 | hp1 | a0001 | c0006 | t0001 | g0128 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01109 | hp1 | a0004 | c0007 | t0001 | g0105 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0040 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0040 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | IBS | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01891 | hp1 | a0001 | c0002 | t0006 | g0035 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02015 | hp1 | a0005 | c0005 | t0001 | g0172 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | CDX | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CDX | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0097 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02738 | hp1 | a0001 | c0001 | t0014 | g0195 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0110 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02922 | hp1 | a0001 | c0002 | t0006 | g0036 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0036 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03225 | hp1 | a0001 | c0002 | t0009 | g0197 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03239 | hp2 | a0002 | c0003 | t0002 | g0085 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0022 | SAS | STU | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04184 | hp1 | a0002 | c0003 | t0012 | g0084 | SAS | BEB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | STU | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0022 | SAS | STU | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | STU | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | STU | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0153 | AFR | YRI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18522 | hp2 | a0001 | c0002 | t0006 | g0035 | AFR | YRI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | YRI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18974 | hp1 | a0001 | c0001 | t0010 | g0071 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18987 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0072 | AFR | LWK | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | LWK | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19065 | hp2 | a0001 | c0008 | t0001 | g0136 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA19240 | hp2 | a0001 | c0002 | t0009 | g0196 | AFR | YRI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ASW | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ASW | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | TSI | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20905 | hp1 | a0002 | c0003 | t0002 | g0022 | SAS | GIH | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | GIH | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG02559 | hp2 | a0001 | c0002 | t0006 | g0064 | AFR | ACB | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | MSL | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | USA | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | USA | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | USA | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0090 | REF | REF | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0047 | REF | REF | RNF103_chr2_86598398_86628865 | RNF103 | chr2 | 86598398 | 86628865 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86603934 | C | T | 1 | a0004 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1967G>A | p.Arg656Gln | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 4/4 | 2946/3482 | 1967/2058 | 656/685 | chr2 | 86603934 | |||
| chr2:86604217 | G | A | 1 | a0005 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1684C>T | p.His562Tyr | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 4/4 | 2663/3482 | 1684/2058 | 562/685 | chr2 | 86604217 | |||
| chr2:86604628 | G | C | 1 | a0003 | 3 | HG01069.hp2 HG01071.hp1 HG01081.hp1 |
missense_variant | MODERATE | c.1273C>G | p.Leu425Val | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 4/4 | 2252/3482 | 1273/2058 | 425/685 | chr2 | 86604628 | |||
| chr2:86612241 | T | C | 1 | a0002 | 5 | HG03239.hp2 HG04115.hp2 HG04184.hp1 others(2): Show |
missense_variant | MODERATE | c.400A>G | p.Lys134Glu | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/4 | 1379/3482 | 400/2058 | 134/685 | chr2 | 86612241 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86604527 | C | G | 1 | a0001c0006 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.1374G>C | p.Leu458Leu | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 4/4 | 2353/3482 | 1374/2058 | 458/685 | chr2 | 86604527 | |||
| chr2:86605139 | A | G | 1 | a0005c0005 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.762T>C | p.Ser254Ser | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 4/4 | 1741/3482 | 762/2058 | 254/685 | chr2 | 86605139 | |||
| chr2:86605271 | T | C | 2 | a0001c0002 a0004c0007 |
28 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(25): Show |
synonymous_variant | LOW | c.630A>G | p.Ala210Ala | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 4/4 | 1609/3482 | 630/2058 | 210/685 | chr2 | 86605271 | |||
| chr2:86612185 | G | A | 1 | a0001c0008 | 1 | NA19065.hp2 | synonymous_variant | LOW | c.456C>T | p.Gly152Gly | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/4 | 1435/3482 | 456/2058 | 152/685 | chr2 | 86612185 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86603468 | C | T | 1 | a0002c0003t0012 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*375G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 4/4 | 375 | chr2 | 86603468 | ||||||
| chr2:86603753 | C | A | 3 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0013 |
21 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*90G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 4/4 | 90 | chr2 | 86603753 | ||||||
| chr2:86622899 | T | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
5_prime_UTR_variant | MODIFIER | c.-13A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | 13 | chr2 | 86622899 | ||||||
| chr2:86623156 | A | G | 1 | a0001c0001t0008 | 2 | HG01257.hp2 HG01258.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-270T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | chr2 | 86623156 | |||||||
| chr2:86623346 | G | A | 1 | a0001c0001t0004 | 7 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-460C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | 460 | chr2 | 86623346 | ||||||
| chr2:86623371 | C | T | 1 | a0001c0001t0005 | 6 | HG01243.hp2 HG01261.hp2 HG02896.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-485G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | 485 | chr2 | 86623371 | ||||||
| chr2:86623635 | G | T | 1 | a0001c0001t0011 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-749C>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | 749 | chr2 | 86623635 | ||||||
| chr2:86623675 | A | G | 1 | a0001c0001t0004 | 7 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-789T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | chr2 | 86623675 | |||||||
| chr2:86623681 | G | A | 1 | a0001c0001t0014 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-795C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | 795 | chr2 | 86623681 | ||||||
| chr2:86623810 | C | G | 1 | a0001c0001t0010 | 1 | NA18974.hp1 | 5_prime_UTR_variant | MODIFIER | c.-924G>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | 924 | chr2 | 86623810 | ||||||
| chr2:86623855 | C | T | 3 | a0001c0001t0003 a0001c0001t0007 a0001c0002t0006 |
25 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-969G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | 969 | chr2 | 86623855 | ||||||
| chr2:86623858 | G | A | 1 | a0001c0002t0009 | 2 | HG03225.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-972C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | 972 | chr2 | 86623858 | ||||||
| chr2:86623859 | A | C | 1 | a0001c0001t0007 | 4 | NA18940.hp1 NA18952.hp1 NA18966.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-973T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/4 | 973 | chr2 | 86623859 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86605565 | A | G | 12 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(9): Show |
21 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.483-147T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86605565 | |||||||
| chr2:86605762 | TTAA | T | 13 | a0001c0001t0001g0148 a0001c0001t0002g0005 a0001c0001t0002g0023 others(10): Show |
28 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.483-347_483-345del others(3): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86605762 | |||||||
| chr2:86606182 | A | C | 15 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0148 others(12): Show |
31 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.483-764T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606182 | |||||||
| chr2:86606184 | T | G | 15 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0148 others(12): Show |
31 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.483-766A>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606184 | |||||||
| chr2:86606186 | A | T | 15 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0148 others(12): Show |
31 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.483-768T>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606186 | |||||||
| chr2:86606187 | TCCC | T | 15 | a0001c0001t0001g0051 a0001c0001t0001g0114 a0001c0001t0001g0148 others(12): Show |
31 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.483-772_483-770del others(3): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606187 | |||||||
| chr2:86606191 | C | G | 12 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(9): Show |
21 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.483-773G>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606191 | |||||||
| chr2:86606213 | A | G | 1 | a0001c0001t0001g0029 | 3 | NA18959.hp2 NA18969.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.483-795T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606213 | |||||||
| chr2:86606236 | T | G | 1 | a0001c0001t0001g0030 | 3 | HG00099.hp2 HG02698.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.483-818A>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606236 | |||||||
| chr2:86606393 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0178 |
2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.483-975T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606393 | |||||||
| chr2:86606397 | G | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0178 |
2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.483-979C>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606397 | |||||||
| chr2:86606403 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0178 |
2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.483-985T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606403 | |||||||
| chr2:86606413 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.483-995G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606413 | |||||||
| chr2:86606449 | A | G | 15 | a0001c0002t0001g0008 a0001c0002t0001g0099 a0001c0002t0001g0100 others(12): Show |
20 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.483-1031T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606449 | |||||||
| chr2:86606459 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0049 others(22): Show |
43 | HG00423.hp2 HG00673.hp2 HG02027.hp2 others(40): Show |
intron_variant | MODIFIER | c.483-1041A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606459 | |||||||
| chr2:86606480 | T | C | 4 | a0001c0001t0003g0069 a0001c0002t0006g0036 a0001c0002t0006g0064 others(1): Show |
7 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-1062A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606480 | |||||||
| chr2:86606508 | T | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0083 |
4 | HG02056.hp2 HG02080.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-1090A>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606508 | |||||||
| chr2:86606662 | C | CA | 5 | a0001c0001t0001g0051 a0001c0001t0001g0113 a0001c0001t0001g0148 others(2): Show |
7 | HG01884.hp2 HG01934.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.483-1245dupT | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606662 | |||||||
| chr2:86606662 | CAA | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
269 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(266): Show |
intron_variant | MODIFIER | c.483-1246_483-1245d others(4): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606662 | |||||||
| chr2:86606662 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0005g0019 a0001c0001t0005g0020 |
6 | HG01243.hp2 HG01261.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.483-1257_483-1245d others(15): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606662 | |||||||
| chr2:86606675 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(58): Show |
167 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.483-1257T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606675 | |||||||
| chr2:86606684 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(30): Show |
55 | HG00423.hp2 HG00673.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.483-1266T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606684 | |||||||
| chr2:86606938 | T | C | 2 | a0001c0001t0005g0019 a0001c0001t0005g0020 |
6 | HG01243.hp2 HG01261.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.483-1520A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86606938 | |||||||
| chr2:86607013 | TTTAG | T | 1 | a0001c0001t0004g0007 | 5 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.483-1599_483-1596d others(6): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607013 | |||||||
| chr2:86607052 | T | A | 1 | a0002c0003t0002g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.483-1634A>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607052 | |||||||
| chr2:86607098 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(30): Show |
55 | HG00423.hp2 HG00673.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.483-1680T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607098 | |||||||
| chr2:86607187 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0170 a0001c0001t0001g0174 others(1): Show |
7 | HG02071.hp1 HG02132.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-1769A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607187 | |||||||
| chr2:86607347 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.483-1929G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607347 | |||||||
| chr2:86607396 | G | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(31): Show |
56 | HG00423.hp2 HG00673.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.483-1978C>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607396 | |||||||
| chr2:86607448 | A | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0079 |
5 | HG01928.hp2 HG01943.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.483-2030T>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607448 | |||||||
| chr2:86607502 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.483-2084A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607502 | |||||||
| chr2:86607503 | TGTTGA | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0146 a0001c0001t0001g0152 |
6 | HG01884.hp1 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.483-2090_483-2086d others(7): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607503 | |||||||
| chr2:86607752 | T | A | 34 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(31): Show |
49 | HG00738.hp2 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.483-2334A>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86607752 | |||||||
| chr2:86608048 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.483-2630C>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608048 | |||||||
| chr2:86608119 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.483-2701C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608119 | |||||||
| chr2:86608200 | G | A | 34 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(31): Show |
49 | HG00738.hp2 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.483-2782C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608200 | |||||||
| chr2:86608385 | G | T | 2 | a0001c0001t0004g0007 a0001c0001t0004g0039 |
7 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-2967C>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608385 | |||||||
| chr2:86608394 | C | T | 5 | a0001c0002t0001g0108 a0001c0002t0001g0110 a0001c0002t0001g0111 others(2): Show |
5 | HG02451.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.483-2976G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608394 | |||||||
| chr2:86608457 | A | G | 9 | a0001c0001t0001g0026 a0001c0001t0001g0145 a0001c0001t0001g0147 others(6): Show |
11 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.483-3039T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608457 | |||||||
| chr2:86608486 | C | CA | 14 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0058 others(11): Show |
18 | HG00280.hp1 HG00323.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.483-3069dupT | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608486 | |||||||
| chr2:86608486 | CA | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0121 a0001c0001t0001g0135 others(8): Show |
13 | HG00673.hp1 HG01496.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-3069delT | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608486 | |||||||
| chr2:86608486 | CAAAAA | C | 8 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0038 others(5): Show |
16 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.483-3073_483-3069d others(7): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608486 | |||||||
| chr2:86608486 | CAAAAAA | C | 6 | a0001c0001t0003g0037 a0001c0001t0003g0065 a0001c0001t0003g0066 others(3): Show |
9 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.483-3074_483-3069d others(8): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608486 | |||||||
| chr2:86608579 | T | C | 2 | a0001c0001t0004g0007 a0001c0001t0004g0039 |
7 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.483-3161A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608579 | |||||||
| chr2:86608673 | A | G | 1 | a0001c0001t0013g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.483-3255T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608673 | |||||||
| chr2:86608681 | T | G | 15 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(12): Show |
26 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.483-3263A>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608681 | |||||||
| chr2:86608792 | C | CA | 14 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(11): Show |
25 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.482+3366dupT | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608792 | |||||||
| chr2:86608809 | A | G | 6 | a0001c0001t0003g0037 a0001c0001t0003g0065 a0001c0001t0003g0066 others(3): Show |
9 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+3350T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608809 | |||||||
| chr2:86608842 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(60): Show |
173 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.482+3317A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608842 | |||||||
| chr2:86608846 | C | T | 34 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(31): Show |
49 | HG00738.hp2 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.482+3313G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86608846 | |||||||
| chr2:86609286 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.482+2873G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86609286 | |||||||
| chr2:86609382 | G | T | 1 | a0002c0003t0012g0084 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.482+2777C>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86609382 | |||||||
| chr2:86609384 | A | AT | 15 | a0001c0001t0001g0026 a0001c0001t0001g0113 a0001c0001t0001g0114 others(12): Show |
17 | HG00140.hp2 HG00408.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.482+2774dupA | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86609384 | |||||||
| chr2:86609384 | A | ATTTT | 14 | a0001c0002t0001g0008 a0001c0002t0001g0099 a0001c0002t0001g0101 others(11): Show |
18 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.482+2771_482+2774d others(6): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86609384 | |||||||
| chr2:86609384 | AT | A | 20 | a0001c0001t0001g0124 a0001c0001t0001g0174 a0001c0001t0001g0182 others(17): Show |
36 | HG00738.hp2 HG01069.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.482+2774delA | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86609384 | |||||||
| chr2:86609387 | T | A | 15 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(12): Show |
26 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.482+2772A>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86609387 | |||||||
| chr2:86609418 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.482+2741A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86609418 | |||||||
| chr2:86609748 | C | T | 34 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(31): Show |
49 | HG00738.hp2 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.482+2411G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86609748 | |||||||
| chr2:86610063 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.482+2096C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86610063 | |||||||
| chr2:86610336 | T | C | 2 | a0001c0001t0004g0007 a0001c0001t0004g0039 |
7 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1823A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86610336 | |||||||
| chr2:86610482 | A | G | 15 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(12): Show |
26 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.482+1677T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86610482 | |||||||
| chr2:86610529 | T | C | 1 | a0001c0001t0002g0089 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.482+1630A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86610529 | |||||||
| chr2:86610574 | C | T | 34 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(31): Show |
49 | HG00738.hp2 HG01069.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.482+1585G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86610574 | |||||||
| chr2:86610861 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0038 a0001c0001t0003g0068 |
6 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.482+1298A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86610861 | |||||||
| chr2:86610867 | A | G | 1 | a0001c0001t0002g0044 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.482+1292T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86610867 | |||||||
| chr2:86611010 | C | CA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.482+1148dupT | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86611010 | |||||||
| chr2:86611067 | T | C | 1 | a0001c0001t0003g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.482+1092A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86611067 | |||||||
| chr2:86611179 | C | CA | 25 | a0001c0001t0001g0187 a0001c0001t0003g0037 a0001c0001t0003g0065 others(22): Show |
35 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.482+979dupT | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86611179 | |||||||
| chr2:86611204 | A | C | 2 | a0001c0001t0002g0042 a0001c0001t0002g0081 |
3 | HG02735.hp2 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.482+955T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86611204 | |||||||
| chr2:86611331 | T | C | 1 | a0001c0002t0001g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.482+828A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86611331 | |||||||
| chr2:86611346 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.482+813G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86611346 | |||||||
| chr2:86611385 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.482+774C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86611385 | |||||||
| chr2:86611405 | T | C | 1 | a0001c0001t0013g0153 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.482+754A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86611405 | |||||||
| chr2:86611742 | C | A | 1 | a0001c0001t0014g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.482+417G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86611742 | |||||||
| chr2:86612030 | T | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0058 others(1): Show |
12 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.482+129A>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86612030 | |||||||
| chr2:86612097 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0092 |
3 | NA18960.hp1 NA18990.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.482+62G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 3/3 | chr2 | 86612097 | |||||||
| chr2:86612348 | TATA | T | 19 | a0001c0002t0001g0008 a0001c0002t0001g0099 a0001c0002t0001g0100 others(16): Show |
23 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.367-77_367-75delTA others(1): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86612348 | |||||||
| chr2:86612407 | C | A | 19 | a0001c0002t0001g0008 a0001c0002t0001g0099 a0001c0002t0001g0100 others(16): Show |
23 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.367-133G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86612407 | |||||||
| chr2:86612534 | T | A | 1 | a0001c0001t0001g0059 | 2 | NA18948.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.367-260A>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86612534 | |||||||
| chr2:86612668 | T | C | 15 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(12): Show |
26 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.367-394A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86612668 | |||||||
| chr2:86612675 | AATTATCA others(8): Show |
A | 1 | a0001c0002t0001g0112 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.367-416_367-402del others(15): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86612675 | |||||||
| chr2:86612697 | A | G | 1 | a0001c0001t0005g0019 | 3 | HG02896.hp1 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.367-423T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86612697 | |||||||
| chr2:86612730 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.367-456T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86612730 | |||||||
| chr2:86612888 | A | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0154 a0001c0001t0001g0162 others(3): Show |
15 | HG00558.hp1 HG00597.hp2 NA18945.hp1 others(12): Show |
intron_variant | MODIFIER | c.367-614T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86612888 | |||||||
| chr2:86612958 | T | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0142 others(19): Show |
31 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.367-684A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86612958 | |||||||
| chr2:86613002 | G | A | 6 | a0001c0001t0003g0037 a0001c0001t0003g0065 a0001c0001t0003g0066 others(3): Show |
9 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-728C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613002 | |||||||
| chr2:86613048 | C | T | 1 | a0001c0001t0001g0056 | 2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.367-774G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613048 | |||||||
| chr2:86613163 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(88): Show |
214 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.367-889T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613163 | |||||||
| chr2:86613171 | A | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(61): Show |
169 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.367-897T>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613171 | |||||||
| chr2:86613182 | C | A | 1 | a0001c0001t0001g0034 | 3 | HG00741.hp1 HG01070.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.367-908G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613182 | |||||||
| chr2:86613202 | G | A | 1 | a0001c0001t0002g0086 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.367-928C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613202 | |||||||
| chr2:86613228 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.367-954G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613228 | |||||||
| chr2:86613292 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0181 |
3 | NA18967.hp1 NA19012.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.367-1018A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613292 | |||||||
| chr2:86613462 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0002g0023 |
5 | HG02809.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-1188G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613462 | |||||||
| chr2:86613516 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.367-1242A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613516 | |||||||
| chr2:86613528 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.367-1254A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613528 | |||||||
| chr2:86613543 | C | A | 15 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(12): Show |
26 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.367-1269G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613543 | |||||||
| chr2:86613568 | C | A | 17 | a0001c0001t0001g0188 a0001c0001t0003g0018 a0001c0001t0003g0037 others(14): Show |
26 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.367-1294G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613568 | |||||||
| chr2:86613673 | G | A | 11 | a0001c0002t0001g0008 a0001c0002t0001g0099 a0001c0002t0001g0100 others(8): Show |
15 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.367-1399C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613673 | |||||||
| chr2:86613687 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.367-1413T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613687 | |||||||
| chr2:86613846 | C | T | 1 | a0001c0001t0001g0054 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.367-1572G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613846 | |||||||
| chr2:86613937 | AT | A | 5 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
5 | NA18747.hp2 NA18951.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.367-1664delA | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613937 | |||||||
| chr2:86613946 | T | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0026 others(28): Show |
45 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.367-1672A>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613946 | |||||||
| chr2:86613979 | G | A | 18 | a0001c0002t0001g0008 a0001c0002t0001g0099 a0001c0002t0001g0100 others(15): Show |
22 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.367-1705C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86613979 | |||||||
| chr2:86614006 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.367-1732G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614006 | |||||||
| chr2:86614007 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.367-1733A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614007 | |||||||
| chr2:86614046 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.367-1772G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614046 | |||||||
| chr2:86614181 | C | G | 15 | a0001c0001t0001g0048 a0001c0001t0002g0005 a0001c0001t0002g0023 others(12): Show |
32 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.367-1907G>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614181 | |||||||
| chr2:86614246 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.367-1972C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614246 | |||||||
| chr2:86614375 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.367-2101C>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614375 | |||||||
| chr2:86614423 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.367-2149C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614423 | |||||||
| chr2:86614448 | C | G | 15 | a0001c0001t0001g0051 a0001c0001t0002g0005 a0001c0001t0002g0023 others(12): Show |
32 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.367-2174G>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614448 | |||||||
| chr2:86614460 | G | A | 16 | a0001c0001t0001g0142 a0001c0001t0003g0017 a0001c0001t0003g0018 others(13): Show |
27 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.367-2186C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614460 | |||||||
| chr2:86614463 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.367-2189G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614463 | |||||||
| chr2:86614614 | A | AG | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(59): Show |
172 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.367-2341dupC | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614614 | |||||||
| chr2:86614652 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.367-2378C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614652 | |||||||
| chr2:86614662 | C | T | 1 | a0001c0001t0001g0053 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.367-2388G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614662 | |||||||
| chr2:86614698 | TTATTGCT others(5): Show |
T | 32 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0026 others(29): Show |
46 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.367-2436_367-2425d others(14): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614698 | |||||||
| chr2:86614756 | A | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.367-2482T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614756 | |||||||
| chr2:86614828 | C | G | 1 | a0001c0001t0003g0067 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.367-2554G>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614828 | |||||||
| chr2:86614951 | G | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0074 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.367-2677C>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614951 | |||||||
| chr2:86614953 | T | C | 4 | a0001c0002t0001g0108 a0001c0002t0001g0109 a0001c0002t0001g0110 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-2679A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86614953 | |||||||
| chr2:86615051 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
177 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.367-2777C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615051 | |||||||
| chr2:86615124 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.367-2850A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615124 | |||||||
| chr2:86615498 | A | AAT | 14 | a0001c0001t0002g0005 a0001c0001t0002g0023 a0001c0001t0002g0041 others(11): Show |
30 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.367-3226_367-3225d others(4): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615498 | |||||||
| chr2:86615520 | T | TTA | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(75): Show |
197 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.367-3248_367-3247d others(4): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATA | 3 | a0001c0001t0001g0186 a0001c0001t0004g0007 a0001c0001t0004g0039 |
8 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.367-3252_367-3247d others(8): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.367-3256_367-3247d others(12): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0115 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.367-3260_367-3247d others(16): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATAT others(9): Show |
4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG00673.hp2 HG01943.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-3262_367-3247d others(18): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATAT others(11): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0048 others(9): Show |
31 | HG01109.hp2 HG02027.hp2 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.367-3264_367-3247d others(20): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATAT others(13): Show |
8 | a0001c0001t0001g0025 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
10 | HG00423.hp2 HG01099.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-3247_367-3246i others(22): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATAT others(15): Show |
3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0145 |
3 | HG01255.hp2 NA18951.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.367-3247_367-3246i others(24): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATAT others(17): Show |
4 | a0001c0001t0001g0050 a0001c0001t0001g0135 a0001c0001t0001g0137 others(1): Show |
5 | NA18943.hp1 NA18983.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.367-3247_367-3246i others(26): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATAT others(19): Show |
1 | a0001c0001t0001g0138 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.367-3247_367-3246i others(28): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615520 | T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.367-3247_367-3246i others(30): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615520 | |||||||
| chr2:86615537 | T | TAA | 1 | a0001c0001t0007g0011 | 4 | NA18940.hp1 NA18952.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-3265_367-3264d others(4): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615537 | |||||||
| chr2:86615584 | A | G | 15 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(12): Show |
26 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.367-3310T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615584 | |||||||
| chr2:86615679 | CAGGA | C | 1 | a0001c0001t0002g0012 | 4 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-3409_367-3406d others(6): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615679 | |||||||
| chr2:86615711 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.367-3437A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615711 | |||||||
| chr2:86615813 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.367-3539G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615813 | |||||||
| chr2:86615894 | T | A | 15 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(12): Show |
26 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.367-3620A>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86615894 | |||||||
| chr2:86616073 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.367-3799G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616073 | |||||||
| chr2:86616293 | T | C | 1 | a0001c0001t0001g0062 | 2 | HG02155.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.367-4019A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616293 | |||||||
| chr2:86616296 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
65 | HG00423.hp2 HG00673.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.367-4022A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616296 | |||||||
| chr2:86616344 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.366+3986T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616344 | |||||||
| chr2:86616365 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(123): Show |
270 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.366+3965G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616365 | |||||||
| chr2:86616438 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.366+3892A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616438 | |||||||
| chr2:86616552 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.366+3778C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616552 | |||||||
| chr2:86616552 | G | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.366+3778C>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616552 | |||||||
| chr2:86616584 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.366+3746A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616584 | |||||||
| chr2:86616635 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
268 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.366+3695G>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616635 | |||||||
| chr2:86616799 | A | G | 4 | a0001c0001t0003g0037 a0001c0002t0006g0035 a0001c0002t0006g0036 others(1): Show |
7 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.366+3531T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616799 | |||||||
| chr2:86616866 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.366+3464T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86616866 | |||||||
| chr2:86617189 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0142 |
8 | HG02486.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.366+3141G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86617189 | |||||||
| chr2:86617215 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.366+3115A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86617215 | |||||||
| chr2:86617244 | G | A | 1 | a0001c0001t0008g0040 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.366+3086C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86617244 | |||||||
| chr2:86617540 | T | TA | 15 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0037 others(12): Show |
26 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.366+2789dupT | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86617540 | |||||||
| chr2:86617568 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.366+2762G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86617568 | |||||||
| chr2:86617600 | G | A | 3 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0111 |
3 | HG02451.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.366+2730C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86617600 | |||||||
| chr2:86617671 | C | A | 20 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0142 others(17): Show |
29 | HG01109.hp1 HG02145.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.366+2659G>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86617671 | |||||||
| chr2:86618057 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.366+2273A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618057 | |||||||
| chr2:86618122 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.366+2208C>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618122 | |||||||
| chr2:86618259 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.366+2071A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618259 | |||||||
| chr2:86618315 | T | C | 1 | a0001c0001t0002g0044 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.366+2015A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618315 | |||||||
| chr2:86618332 | A | C | 1 | a0001c0001t0002g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.366+1998T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618332 | |||||||
| chr2:86618386 | G | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0145 others(7): Show |
15 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.366+1944C>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618386 | |||||||
| chr2:86618427 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.366+1903T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618427 | |||||||
| chr2:86618574 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.366+1756T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618574 | |||||||
| chr2:86618591 | T | C | 1 | a0001c0001t0001g0063 | 2 | HG00609.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.366+1739A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618591 | |||||||
| chr2:86618617 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.366+1713T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618617 | |||||||
| chr2:86618929 | A | T | 1 | a0001c0001t0002g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.366+1401T>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618929 | |||||||
| chr2:86618995 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.366+1335A>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86618995 | |||||||
| chr2:86619125 | A | G | 2 | a0001c0002t0001g0099 a0001c0002t0001g0100 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.366+1205T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86619125 | |||||||
| chr2:86619220 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.366+1110C>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86619220 | |||||||
| chr2:86619276 | T | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0014 others(68): Show |
113 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.366+1054A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86619276 | |||||||
| chr2:86619366 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.366+964A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86619366 | |||||||
| chr2:86619418 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.366+912G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86619418 | |||||||
| chr2:86619544 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.366+786G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86619544 | |||||||
| chr2:86619548 | G | C | 1 | a0001c0002t0001g0112 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.366+782C>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86619548 | |||||||
| chr2:86619739 | A | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.366+591T>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86619739 | |||||||
| chr2:86619927 | T | A | 1 | a0001c0001t0002g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.366+403A>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86619927 | |||||||
| chr2:86620146 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.366+184A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86620146 | |||||||
| chr2:86620291 | A | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.366+39T>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 2/3 | chr2 | 86620291 | |||||||
| chr2:86620497 | T | G | 1 | a0001c0001t0001g0152 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.227-28A>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86620497 | |||||||
| chr2:86620912 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.227-443A>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86620912 | |||||||
| chr2:86620921 | C | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.227-452G>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86620921 | |||||||
| chr2:86620998 | T | A | 1 | a0001c0001t0001g0189 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.227-529A>T | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86620998 | |||||||
| chr2:86621062 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.227-593T>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86621062 | |||||||
| chr2:86621073 | T | C | 9 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0038 others(6): Show |
17 | HG00738.hp2 HG01069.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.227-604A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86621073 | |||||||
| chr2:86621301 | TA | T | 3 | a0001c0001t0002g0045 a0001c0001t0002g0092 a0001c0001t0002g0093 |
4 | NA18960.hp1 NA18990.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-833delT | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86621301 | |||||||
| chr2:86621678 | AAAG | A | 13 | a0001c0001t0002g0005 a0001c0001t0002g0023 a0001c0001t0002g0045 others(10): Show |
28 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.226+980_226+982del others(3): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86621678 | |||||||
| chr2:86621691 | A | C | 2 | a0001c0001t0005g0019 a0001c0001t0005g0020 |
6 | HG01243.hp2 HG01261.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+970T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86621691 | |||||||
| chr2:86621721 | AATACTTG others(23): Show |
A | 1 | a0001c0001t0001g0191 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.226+910_226+939del others(30): Show |
RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86621721 | |||||||
| chr2:86621770 | C | T | 18 | a0001c0002t0001g0008 a0001c0002t0001g0099 a0001c0002t0001g0100 others(15): Show |
22 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.226+891G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86621770 | |||||||
| chr2:86621803 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0074 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.226+858G>A | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86621803 | |||||||
| chr2:86622053 | G | GA | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(64): Show |
178 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.226+607dupT | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86622053 | |||||||
| chr2:86622253 | T | C | 1 | a0001c0002t0001g0192 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.226+408A>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86622253 | |||||||
| chr2:86622370 | A | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.226+291T>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86622370 | |||||||
| chr2:86622534 | G | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02165.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.226+127C>G | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86622534 | |||||||
| chr2:86622649 | C | G | 2 | a0001c0001t0004g0007 a0001c0001t0004g0039 |
7 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+12G>C | RNF103 | ENSG00000239305.7 | transcript | ENST00000237455.5 | protein_coding | 1/3 | chr2 | 86622649 |