Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56254 |
| ensemblid | ENSG00000155827.12 |
| hgncid | 10062 |
| symbol | RNF20 |
| name | ring finger protein 20 |
| refseq_nuc | NM_019592.7 |
| refseq_prot | NP_062538.5 |
| ensembl_nuc | ENST00000389120.8 |
| ensembl_prot | ENSP00000373772.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 101533853 |
| end | 101563344 |
| strand | + |
| ver | v1.2 |
| region | chr9:101533853-101563344 |
| region5000 | chr9:101528853-101568344 |
| regionname0 | RNF20_chr9_101533853_101563344 |
| regionname5000 | RNF20_chr9_101528853_101568344 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 975 | 398 | 84 | 80 | 176 | 16 | 40 | 139 | RNF20_chr9_101528853_101568344 | RNF20 | MSGIG others(970): Show |
chr9 | 101528853 | 101568344 |
| a0002 | 0/0 | 975 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | MSGIG others(970): Show |
chr9 | 101528853 | 101568344 |
| a0003 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | MSGIG others(970): Show |
chr9 | 101528853 | 101568344 |
| a0004 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | MSGIG others(970): Show |
chr9 | 101528853 | 101568344 |
| a0005 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | MSGIG others(970): Show |
chr9 | 101528853 | 101568344 |
| a0006 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | MSGIG others(970): Show |
chr9 | 101528853 | 101568344 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2925 | 224 | 64 | 50 | 84 | 9 | 16 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0002 | 0/0 | 2925 | 77 | 0 | 9 | 55 | 2 | 11 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0003 | 0/0 | 2925 | 57 | 14 | 11 | 22 | 5 | 5 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0004 | 0/1 | 2925 | 28 | 0 | 9 | 13 | 0 | 5 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0006 | 0/0 | 2925 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0007 | 0/0 | 2925 | 3 | 0 | 0 | 0 | 0 | 3 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0009 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0010 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0011 | 0/0 | 2925 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0012 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0001c0015 | 0/0 | 2925 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0002c0005 | 0/0 | 2925 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0003c0014 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0004c0008 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0005c0016 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 | ||
| a0006c0013 | 0/0 | 2925 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | ATGTC others(2920): Show |
chr9 | 101528853 | 101568344 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3938 | 216 | 59 | 48 | 84 | 8 | 16 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0001t0005 | 0/0 | 3938 | 3 | 3 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0001t0006 | 0/0 | 3938 | 2 | 0 | 1 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0001t0008 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0001t0009 | 0/0 | 3938 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0001t0010 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0002t0001 | 0/0 | 3938 | 74 | 0 | 9 | 52 | 2 | 11 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0002t0004 | 0/0 | 3938 | 3 | 0 | 0 | 3 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0003t0001 | 0/0 | 3938 | 57 | 14 | 11 | 22 | 5 | 5 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0004t0002 | 0/1 | 3938 | 19 | 0 | 1 | 13 | 0 | 4 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0004t0003 | 0/0 | 3938 | 9 | 0 | 8 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0006t0001 | 0/0 | 3938 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0007t0001 | 0/0 | 3938 | 3 | 0 | 0 | 0 | 0 | 3 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0009t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0010t0001 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0011t0007 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0012t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0001c0015t0001 | 0/0 | 3938 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0002c0005t0001 | 0/0 | 3938 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0003c0014t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0004c0008t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0005c0016t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| a0006c0013t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | AAGTT others(3933): Show |
chr9 | 101528853 | 101568344 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 40 | 6 | 10 | 18 | 3 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0003 | 0/0 | 22 | 1 | 4 | 16 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0004 | 0/0 | 22 | 2 | 5 | 14 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0008 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0009 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0014 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0005g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0001 | 0/0 | 46 | 0 | 5 | 33 | 1 | 7 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0002t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0005 | 0/0 | 16 | 0 | 4 | 10 | 1 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0007 | 0/0 | 9 | 0 | 4 | 0 | 4 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0004t0002g0006 | 0/1 | 13 | 0 | 1 | 7 | 0 | 4 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0004t0002g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0004t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0004t0003g0011 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0004t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0004t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0004t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0006t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0006t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0006t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0007t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0007t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0009t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0010t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0011t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0012t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0001c0015t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0002c0005t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0002c0005t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0002c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0003c0014t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0004c0008t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0005c0016t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| a0006c0013t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0007 | EUR | GBR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0005 | EUR | GBR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0119 | EUR | FIN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00733 | hp2 | a0001 | c0004 | t0003 | g0011 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01070 | hp1 | a0001 | c0004 | t0003 | g0054 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0121 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01099 | hp1 | a0001 | c0004 | t0003 | g0011 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01192 | hp1 | a0001 | c0004 | t0003 | g0011 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0135 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0003 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01256 | hp1 | a0001 | c0004 | t0003 | g0011 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01258 | hp2 | a0001 | c0004 | t0003 | g0011 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0143 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0144 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01496 | hp2 | a0001 | c0004 | t0002 | g0006 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0099 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01981 | hp1 | a0001 | c0004 | t0003 | g0011 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02080 | hp1 | a0001 | c0004 | t0002 | g0012 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02129 | hp2 | a0001 | c0004 | t0002 | g0012 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02148 | hp1 | a0001 | c0015 | t0001 | g0001 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02165 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | CDX | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02165 | hp2 | a0001 | c0004 | t0002 | g0012 | EAS | CDX | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02280 | hp2 | a0001 | c0011 | t0007 | g0061 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02293 | hp2 | a0001 | c0004 | t0003 | g0053 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02523 | hp2 | a0003 | c0014 | t0001 | g0031 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02622 | hp2 | a0001 | c0010 | t0001 | g0104 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0149 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02647 | hp2 | a0001 | c0006 | t0001 | g0038 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02698 | hp2 | a0001 | c0004 | t0002 | g0006 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02735 | hp2 | a0001 | c0004 | t0002 | g0006 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0120 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02886 | hp2 | a0001 | c0006 | t0001 | g0112 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0148 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0147 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03130 | hp2 | a0002 | c0005 | t0001 | g0023 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0102 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03491 | hp2 | a0001 | c0007 | t0001 | g0045 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03710 | hp1 | a0001 | c0004 | t0002 | g0006 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03710 | hp2 | a0001 | c0007 | t0001 | g0045 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03834 | hp2 | a0001 | c0004 | t0002 | g0006 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0043 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03942 | hp2 | a0001 | c0007 | t0001 | g0136 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0043 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG04228 | hp1 | a0001 | c0004 | t0003 | g0051 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18522 | hp1 | a0002 | c0005 | t0001 | g0023 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18612 | hp2 | a0001 | c0004 | t0002 | g0006 | EAS | CHB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18747 | hp2 | a0001 | c0009 | t0001 | g0059 | EAS | CHB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18906 | hp2 | a0002 | c0005 | t0001 | g0048 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18948 | hp1 | a0004 | c0008 | t0001 | g0133 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18961 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18962 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18970 | hp2 | a0001 | c0004 | t0002 | g0012 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18971 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18971 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18984 | hp2 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18985 | hp1 | a0001 | c0012 | t0001 | g0017 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18993 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19002 | hp2 | a0001 | c0004 | t0002 | g0052 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19010 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0111 | AFR | LWK | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19054 | hp2 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19055 | hp1 | a0005 | c0016 | t0001 | g0065 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19057 | hp1 | a0006 | c0013 | t0001 | g0058 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19060 | hp2 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19068 | hp2 | a0001 | c0004 | t0002 | g0012 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA19240 | hp2 | a0001 | c0006 | t0001 | g0038 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ASW | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ASW | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0007 | EUR | TSI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0142 | SAS | GIH | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | GIH | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG06807 | hp1 | a0002 | c0005 | t0001 | g0002 | AFR | USA | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | USA | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | USA | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0002 | g0006 | REF | REF | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:101540967 | A | G | 1 | a0005 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.620A>G | p.Asn207Ser | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/20 | 708/3938 | 620/2928 | 207/975 | chr9 | 101540967 | |||
| chr9:101551685 | G | A | 1 | a0004 | 1 | NA18948.hp1 | missense_variant&splice_region_variant | MODERATE | c.1274G>A | p.Arg425Gln | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 11/20 | 1362/3938 | 1274/2928 | 425/975 | chr9 | 101551685 | |||
| chr9:101552453 | C | T | 1 | a0003 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1601C>T | p.Ala534Val | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/20 | 1689/3938 | 1601/2928 | 534/975 | chr9 | 101552453 | |||
| chr9:101552664 | A | C | 1 | a0006 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1812A>C | p.Arg604Ser | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/20 | 1900/3938 | 1812/2928 | 604/975 | chr9 | 101552664 | |||
| chr9:101561177 | G | A | 1 | a0002 | 4 | HG03130.hp2 HG06807.hp1 NA18522.hp1 others(1): Show |
missense_variant | MODERATE | c.2596G>A | p.Val866Met | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 18/20 | 2684/3938 | 2596/2928 | 866/975 | chr9 | 101561177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:101540343 | A | G | 1 | a0001c0004 | 27 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(24): Show |
synonymous_variant | LOW | c.270A>G | p.Leu90Leu | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 3/20 | 358/3938 | 270/2928 | 90/975 | chr9 | 101540343 | |||
| chr9:101544780 | G | T | 1 | a0001c0007 | 3 | HG03491.hp2 HG03710.hp2 HG03942.hp2 |
synonymous_variant | LOW | c.642G>T | p.Val214Val | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/20 | 730/3938 | 642/2928 | 214/975 | chr9 | 101544780 | |||
| chr9:101547163 | T | C | 2 | a0001c0003 a0004c0008 |
58 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(55): Show |
synonymous_variant | LOW | c.921T>C | p.Tyr307Tyr | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 8/20 | 1009/3938 | 921/2928 | 307/975 | chr9 | 101547163 | |||
| chr9:101547172 | G | C | 1 | a0001c0009 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.930G>C | p.Gly310Gly | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 8/20 | 1018/3938 | 930/2928 | 310/975 | chr9 | 101547172 | |||
| chr9:101547416 | A | G | 1 | a0001c0015 | 1 | HG02148.hp1 | synonymous_variant | LOW | c.990A>G | p.Ala330Ala | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/20 | 1078/3938 | 990/2928 | 330/975 | chr9 | 101547416 | |||
| chr9:101550656 | T | C | 1 | a0001c0010 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1143T>C | p.Tyr381Tyr | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/20 | 1231/3938 | 1143/2928 | 381/975 | chr9 | 101550656 | |||
| chr9:101552733 | A | G | 1 | a0001c0006 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
synonymous_variant | LOW | c.1881A>G | p.Lys627Lys | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/20 | 1969/3938 | 1881/2928 | 627/975 | chr9 | 101552733 | |||
| chr9:101554063 | C | T | 1 | a0001c0012 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.1977C>T | p.Asp659Asp | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/20 | 2065/3938 | 1977/2928 | 659/975 | chr9 | 101554063 | |||
| chr9:101554087 | G | A | 1 | a0001c0011 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2001G>A | p.Glu667Glu | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/20 | 2089/3938 | 2001/2928 | 667/975 | chr9 | 101554087 | |||
| chr9:101562263 | G | A | 5 | a0001c0002 a0001c0009 a0001c0012 others(2): Show |
81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
synonymous_variant | LOW | c.2769G>A | p.Pro923Pro | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 2857/3938 | 2769/2928 | 923/975 | chr9 | 101562263 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:101533882 | G | C | 1 | a0001c0002t0004 | 3 | NA18962.hp2 NA18971.hp2 NA18993.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/20 | 1542 | chr9 | 101533882 | ||||||
| chr9:101533899 | C | A | 1 | a0001c0011t0007 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42C>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/20 | 1525 | chr9 | 101533899 | ||||||
| chr9:101535411 | T | A | 2 | a0001c0004t0002 a0001c0004t0003 |
27 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-13T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/20 | 13 | chr9 | 101535411 | ||||||
| chr9:101562581 | G | A | 1 | a0001c0001t0008 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 159 | chr9 | 101562581 | ||||||
| chr9:101562652 | T | C | 1 | a0001c0001t0009 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*230T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 230 | chr9 | 101562652 | ||||||
| chr9:101562920 | C | T | 2 | a0001c0001t0006 a0001c0004t0002 |
20 | HG00280.hp2 HG01081.hp1 HG01496.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*498C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 498 | chr9 | 101562920 | ||||||
| chr9:101563068 | T | A | 1 | a0001c0001t0010 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*646T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 646 | chr9 | 101563068 | ||||||
| chr9:101563205 | A | G | 1 | a0001c0001t0005 | 3 | HG02976.hp2 HG03098.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*783A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 783 | chr9 | 101563205 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:101533991 | A | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(51): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.-27+77A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101533991 | |||||||
| chr9:101534036 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+122G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534036 | |||||||
| chr9:101534061 | A | G | 1 | a0001c0003t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-27+147A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534061 | |||||||
| chr9:101534462 | G | C | 2 | a0002c0005t0001g0023 a0002c0005t0001g0048 |
3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-27+548G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534462 | |||||||
| chr9:101534549 | ATTCT | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+640_-27+643del others(4): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 101534549 | ||||||
| chr9:101534669 | A | G | 12 | a0001c0003t0001g0007 a0001c0003t0001g0010 a0001c0003t0001g0142 others(9): Show |
26 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-26-729A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534669 | |||||||
| chr9:101534909 | CT | C | 7 | a0001c0001t0001g0025 a0001c0004t0002g0006 a0001c0004t0002g0012 others(4): Show |
28 | HG00733.hp2 HG01099.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.-26-473delT | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 101534909 | ||||||
| chr9:101534930 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-26-468C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534930 | |||||||
| chr9:101535024 | T | C | 7 | a0001c0004t0002g0006 a0001c0004t0002g0012 a0001c0004t0002g0052 others(4): Show |
27 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.-26-374T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535024 | |||||||
| chr9:101535049 | C | A | 7 | a0001c0004t0002g0006 a0001c0004t0002g0012 a0001c0004t0002g0052 others(4): Show |
27 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.-26-349C>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535049 | |||||||
| chr9:101535049 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-26-349C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535049 | |||||||
| chr9:101535109 | G | A | 1 | a0002c0005t0001g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-26-289G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535109 | |||||||
| chr9:101535202 | C | G | 3 | a0001c0006t0001g0038 a0001c0006t0001g0111 a0001c0006t0001g0112 |
4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-196C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535202 | |||||||
| chr9:101535233 | AT | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
7 | HG02280.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-151delT | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 101535233 | ||||||
| chr9:101535561 | A | G | 1 | a0001c0006t0001g0112 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.129+9A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101535561 | |||||||
| chr9:101535753 | T | C | 1 | a0006c0013t0001g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.129+201T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101535753 | |||||||
| chr9:101535874 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.129+322C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101535874 | |||||||
| chr9:101536019 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0109 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.129+467A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536019 | |||||||
| chr9:101536102 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.129+550A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536102 | |||||||
| chr9:101536152 | A | C | 3 | a0001c0003t0001g0047 a0001c0003t0001g0140 a0001c0003t0001g0141 |
4 | NA18965.hp2 NA18974.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+600A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536152 | |||||||
| chr9:101536243 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0010g0102 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.129+691T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536243 | |||||||
| chr9:101536424 | G | C | 5 | a0001c0003t0001g0007 a0001c0003t0001g0142 a0001c0003t0001g0143 others(2): Show |
13 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.129+872G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536424 | |||||||
| chr9:101536464 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA18986.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.129+912A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536464 | |||||||
| chr9:101536776 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.129+1224A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536776 | |||||||
| chr9:101536803 | G | A | 1 | a0001c0009t0001g0059 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.129+1251G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536803 | |||||||
| chr9:101536917 | T | C | 7 | a0001c0004t0002g0006 a0001c0004t0002g0012 a0001c0004t0002g0052 others(4): Show |
27 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.129+1365T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536917 | |||||||
| chr9:101536933 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.129+1381C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536933 | |||||||
| chr9:101537011 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(35): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.129+1459C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537011 | |||||||
| chr9:101537021 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.129+1469C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537021 | |||||||
| chr9:101537050 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.129+1498G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537050 | |||||||
| chr9:101537197 | A | T | 1 | a0001c0001t0001g0036 | 2 | NA18939.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.129+1645A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537197 | |||||||
| chr9:101537203 | G | C | 1 | a0001c0001t0001g0013 | 5 | HG00140.hp2 HG01257.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+1651G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537203 | |||||||
| chr9:101537221 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.129+1669A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537221 | |||||||
| chr9:101537277 | G | A | 1 | a0001c0002t0001g0060 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.129+1725G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537277 | |||||||
| chr9:101537283 | T | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(35): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.129+1731T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537283 | |||||||
| chr9:101537523 | TG | T | 7 | a0001c0004t0002g0006 a0001c0004t0002g0012 a0001c0004t0002g0052 others(4): Show |
27 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.129+1974delG | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 101537523 | ||||||
| chr9:101537539 | G | A | 1 | a0001c0011t0007g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.129+1987G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537539 | |||||||
| chr9:101537591 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(35): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.129+2039A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537591 | |||||||
| chr9:101537798 | A | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(91): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.129+2246A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537798 | |||||||
| chr9:101537842 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | NA18986.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.129+2290A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537842 | |||||||
| chr9:101537942 | A | T | 1 | a0001c0001t0001g0030 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.130-2261A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537942 | |||||||
| chr9:101537994 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0109 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130-2209G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537994 | |||||||
| chr9:101537995 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130-2208A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537995 | |||||||
| chr9:101538169 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.130-2034A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538169 | |||||||
| chr9:101538300 | G | A | 1 | a0001c0004t0003g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.130-1903G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538300 | |||||||
| chr9:101538390 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0010g0102 a0001c0010t0001g0104 |
3 | HG02622.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.130-1813C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538390 | |||||||
| chr9:101538550 | G | C | 3 | a0001c0004t0002g0006 a0001c0004t0002g0012 a0001c0004t0002g0052 |
18 | HG01496.hp2 HG02080.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.130-1653G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538550 | |||||||
| chr9:101538778 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-1425G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538778 | |||||||
| chr9:101538818 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0010g0102 |
2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.130-1385T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538818 | |||||||
| chr9:101538857 | G | T | 1 | a0001c0011t0007g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.130-1346G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538857 | |||||||
| chr9:101538990 | C | T | 3 | a0001c0006t0001g0038 a0001c0006t0001g0111 a0001c0006t0001g0112 |
4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1213C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538990 | |||||||
| chr9:101539224 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(89): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.130-979A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539224 | |||||||
| chr9:101539226 | A | G | 3 | a0001c0004t0002g0006 a0001c0004t0002g0012 a0001c0004t0002g0052 |
18 | HG01496.hp2 HG02080.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.130-977A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539226 | |||||||
| chr9:101539253 | G | T | 1 | a0001c0001t0001g0056 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.130-950G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539253 | |||||||
| chr9:101539274 | C | T | 1 | a0001c0003t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130-929C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539274 | |||||||
| chr9:101539280 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.130-923C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539280 | |||||||
| chr9:101539602 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.130-601C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539602 | |||||||
| chr9:101539661 | A | G | 23 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0017 others(20): Show |
80 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.130-542A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539661 | |||||||
| chr9:101539883 | A | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(89): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.130-320A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539883 | |||||||
| chr9:101539973 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.130-230G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539973 | |||||||
| chr9:101540185 | G | A | 2 | a0001c0001t0001g0152 a0001c0010t0001g0104 |
2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.130-18G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101540185 | |||||||
| chr9:101540453 | C | T | 1 | a0001c0003t0001g0046 | 2 | NA18993.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.298-37C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 3/19 | chr9 | 101540453 | |||||||
| chr9:101540454 | C | G | 1 | a0001c0003t0001g0145 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298-36C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 3/19 | chr9 | 101540454 | |||||||
| chr9:101540676 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0109 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.445+39T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 4/19 | chr9 | 101540676 | |||||||
| chr9:101541018 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628+43A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541018 | |||||||
| chr9:101541295 | T | C | 24 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0017 others(21): Show |
81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.628+320T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541295 | |||||||
| chr9:101541371 | A | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(91): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.628+396A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541371 | |||||||
| chr9:101541399 | A | G | 1 | a0001c0002t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.628+424A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541399 | |||||||
| chr9:101541607 | G | A | 8 | a0001c0004t0002g0006 a0001c0004t0002g0012 a0001c0004t0002g0052 others(5): Show |
28 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.628+632G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541607 | |||||||
| chr9:101541946 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.628+971A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541946 | |||||||
| chr9:101542116 | A | G | 1 | a0001c0010t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.628+1141A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542116 | |||||||
| chr9:101542206 | A | G | 1 | a0001c0004t0003g0053 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.628+1231A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542206 | |||||||
| chr9:101542337 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.628+1362A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542337 | |||||||
| chr9:101542644 | A | G | 1 | a0001c0003t0001g0141 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.628+1669A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542644 | |||||||
| chr9:101542816 | C | T | 23 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0017 others(20): Show |
80 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.628+1841C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542816 | |||||||
| chr9:101542893 | A | T | 1 | a0001c0001t0001g0039 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.629-1874A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542893 | |||||||
| chr9:101542954 | T | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0062 |
3 | HG01934.hp2 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.629-1813T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542954 | |||||||
| chr9:101543266 | A | C | 1 | a0001c0011t0007g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.629-1501A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543266 | |||||||
| chr9:101543295 | G | GCCAGGGC others(17): Show |
9 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0004t0002g0006 others(6): Show |
29 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.629-1424_629-1401d others(26): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543295 | ||||||
| chr9:101543295 | GCCAGGGC others(41): Show |
G | 1 | a0001c0001t0001g0039 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.629-1448_629-1401d others(50): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543295 | ||||||
| chr9:101543372 | G | A | 1 | a0001c0003t0001g0021 | 3 | NA18973.hp2 NA19084.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.629-1395G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543372 | |||||||
| chr9:101543372 | GGCGGCAC others(16): Show |
G | 3 | a0001c0003t0001g0144 a0001c0007t0001g0045 a0001c0007t0001g0136 |
4 | HG01346.hp1 HG03491.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-1356_629-1334d others(25): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543372 | ||||||
| chr9:101543375 | G | GGCACTGT others(17): Show |
1 | a0001c0001t0001g0025 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.629-1379_629-1378i others(26): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543375 | ||||||
| chr9:101543445 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.629-1322G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543445 | |||||||
| chr9:101543468 | A | AGCACTGT others(17): Show |
1 | a0001c0011t0007g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.629-1279_629-1256d others(26): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543468 | ||||||
| chr9:101543468 | A | AGCACTGT others(16): Show |
2 | a0001c0001t0001g0029 a0001c0001t0001g0089 |
3 | HG01167.hp2 HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.629-1286_629-1285i others(25): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543468 | ||||||
| chr9:101543481 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA18973.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.629-1286C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543481 | |||||||
| chr9:101543490 | G | A | 1 | a0001c0003t0001g0040 | 2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.629-1277G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543490 | |||||||
| chr9:101543499 | TCTAACCC others(3): Show |
T | 15 | a0001c0003t0001g0007 a0001c0003t0001g0010 a0001c0003t0001g0142 others(12): Show |
30 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.629-1266_629-1257d others(12): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543499 | ||||||
| chr9:101543539 | C | T | 7 | a0001c0004t0002g0006 a0001c0004t0002g0012 a0001c0004t0002g0052 others(4): Show |
27 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.629-1228C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543539 | |||||||
| chr9:101543583 | AGCGGCAC others(17): Show |
A | 1 | a0001c0001t0001g0044 | 2 | HG01433.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.629-1167_629-1144d others(26): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543583 | ||||||
| chr9:101543592 | G | A | 1 | a0001c0004t0003g0053 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.629-1175G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543592 | |||||||
| chr9:101543679 | T | C | 3 | a0001c0001t0001g0103 a0001c0001t0010g0102 a0001c0010t0001g0104 |
3 | HG02622.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.629-1088T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543679 | |||||||
| chr9:101543737 | C | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0132 a0001c0003t0001g0005 others(9): Show |
34 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.629-1030C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543737 | |||||||
| chr9:101543784 | T | C | 1 | a0001c0010t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.629-983T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543784 | |||||||
| chr9:101543879 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.629-888A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543879 | |||||||
| chr9:101544044 | ACT | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(36): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.629-718_629-717del others(2): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101544044 | ||||||
| chr9:101544146 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.629-621A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544146 | |||||||
| chr9:101544151 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.629-616G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544151 | |||||||
| chr9:101544348 | T | C | 24 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0017 others(21): Show |
81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.629-419T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544348 | |||||||
| chr9:101544564 | G | T | 3 | a0001c0006t0001g0038 a0001c0006t0001g0111 a0001c0006t0001g0112 |
4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-203G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544564 | |||||||
| chr9:101544645 | T | G | 3 | a0001c0002t0001g0015 a0001c0002t0001g0095 a0001c0002t0001g0096 |
7 | HG02015.hp1 HG02071.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.629-122T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544645 | |||||||
| chr9:101544664 | G | A | 2 | a0001c0003t0001g0146 a0001c0003t0001g0151 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.629-103G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544664 | |||||||
| chr9:101544706 | T | TA | 13 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
21 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.629-45dupA | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101544706 | ||||||
| chr9:101544706 | TA | T | 15 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0001g0116 others(12): Show |
35 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.629-45delA | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101544706 | ||||||
| chr9:101544763 | C | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0087 |
2 | HG03540.hp2 NA19030.hp1 |
splice_region_variant&intron_variant | LOW | c.629-4C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544763 | |||||||
| chr9:101545050 | C | A | 1 | a0001c0002t0001g0097 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.747+165C>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545050 | |||||||
| chr9:101545252 | G | C | 23 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0017 others(20): Show |
80 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.747+367G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545252 | |||||||
| chr9:101545351 | T | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0025 others(23): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.747+466T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545351 | |||||||
| chr9:101545418 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.747+533A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545418 | |||||||
| chr9:101545510 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.747+625G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545510 | |||||||
| chr9:101545554 | T | C | 1 | a0001c0011t0007g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.747+669T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545554 | |||||||
| chr9:101545593 | T | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(35): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.747+708T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545593 | |||||||
| chr9:101545629 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0109 |
3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.747+744G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545629 | |||||||
| chr9:101545902 | A | T | 1 | a0001c0010t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.748-918A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545902 | |||||||
| chr9:101545931 | A | C | 1 | a0001c0010t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.748-889A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545931 | |||||||
| chr9:101546083 | A | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(38): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.748-737A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546083 | |||||||
| chr9:101546094 | G | T | 3 | a0001c0006t0001g0038 a0001c0006t0001g0111 a0001c0006t0001g0112 |
4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-726G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546094 | |||||||
| chr9:101546160 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.748-660C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546160 | |||||||
| chr9:101546235 | A | G | 1 | a0001c0001t0001g0027 | 2 | NA18945.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.748-585A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546235 | |||||||
| chr9:101546265 | G | A | 1 | a0001c0011t0007g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.748-555G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546265 | |||||||
| chr9:101546595 | T | G | 1 | a0001c0001t0006g0119 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.748-225T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546595 | |||||||
| chr9:101546646 | GAC | G | 3 | a0001c0006t0001g0038 a0001c0006t0001g0111 a0001c0006t0001g0112 |
4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-170_748-169del others(2): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 101546646 | ||||||
| chr9:101546666 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-154A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546666 | |||||||
| chr9:101546726 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.748-94C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546726 | |||||||
| chr9:101547597 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1092+79C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101547597 | |||||||
| chr9:101547779 | G | T | 1 | a0001c0001t0001g0020 | 3 | HG01167.hp1 HG01361.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1092+261G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101547779 | |||||||
| chr9:101547989 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1092+471A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101547989 | |||||||
| chr9:101548102 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1092+584G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101548102 | |||||||
| chr9:101548829 | A | G | 1 | a0001c0004t0002g0052 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1092+1311A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101548829 | |||||||
| chr9:101548864 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1092+1346C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101548864 | |||||||
| chr9:101548993 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1092+1475C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101548993 | |||||||
| chr9:101549069 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1093-1537T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549069 | |||||||
| chr9:101549081 | C | T | 1 | a0001c0003t0001g0043 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1093-1525C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549081 | |||||||
| chr9:101549112 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1093-1494A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549112 | |||||||
| chr9:101549165 | G | A | 1 | a0001c0001t0008g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1093-1441G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549165 | |||||||
| chr9:101549196 | G | A | 1 | a0001c0002t0001g0069 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1093-1410G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549196 | |||||||
| chr9:101549330 | A | T | 1 | a0001c0002t0001g0035 | 2 | HG02738.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1093-1276A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549330 | |||||||
| chr9:101549429 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG01358.hp1 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1093-1177G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549429 | |||||||
| chr9:101549471 | G | A | 9 | a0001c0001t0006g0119 a0001c0001t0006g0121 a0001c0004t0002g0006 others(6): Show |
29 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1093-1135G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549471 | |||||||
| chr9:101549499 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1093-1107A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549499 | |||||||
| chr9:101549603 | T | C | 1 | a0001c0011t0007g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1093-1003T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549603 | |||||||
| chr9:101549636 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0008g0120 |
3 | HG01070.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1093-970C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549636 | |||||||
| chr9:101549668 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1093-938G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549668 | |||||||
| chr9:101549696 | G | A | 9 | a0001c0001t0006g0119 a0001c0001t0006g0121 a0001c0004t0002g0006 others(6): Show |
29 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1093-910G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549696 | |||||||
| chr9:101549809 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1093-797G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549809 | |||||||
| chr9:101549880 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0088 |
7 | HG00639.hp2 HG01167.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-726G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549880 | |||||||
| chr9:101549920 | A | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0125 a0001c0001t0001g0130 others(2): Show |
6 | HG02258.hp2 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1093-686A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549920 | |||||||
| chr9:101550010 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1093-596C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101550010 | |||||||
| chr9:101550065 | C | T | 25 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0017 others(22): Show |
82 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1093-541C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101550065 | |||||||
| chr9:101550165 | A | C | 24 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0017 others(21): Show |
81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1093-441A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101550165 | |||||||
| chr9:101550500 | T | G | 1 | a0001c0001t0008g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1093-106T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101550500 | |||||||
| chr9:101551147 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1272+362A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551147 | |||||||
| chr9:101551171 | C | G | 47 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(44): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1272+386C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551171 | |||||||
| chr9:101551200 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1272+415A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551200 | |||||||
| chr9:101551215 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1272+430G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551215 | |||||||
| chr9:101551223 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1272+438T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551223 | |||||||
| chr9:101551550 | A | C | 1 | a0001c0003t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1273-134A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551550 | |||||||
| chr9:101551560 | T | C | 2 | a0001c0003t0001g0146 a0001c0003t0001g0151 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1273-124T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551560 | |||||||
| chr9:101551583 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1273-101G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551583 | |||||||
| chr9:101551586 | T | G | 2 | a0001c0006t0001g0038 a0001c0006t0001g0112 |
3 | HG02647.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1273-98T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551586 | |||||||
| chr9:101551616 | C | CATTATTG others(54): Show |
44 | a0001c0001t0001g0037 a0001c0001t0001g0083 a0001c0001t0001g0103 others(41): Show |
117 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1273-66_1273-65ins others(61): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 101551616 | ||||||
| chr9:101551885 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1408+66A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 11/19 | chr9 | 101551885 | |||||||
| chr9:101551946 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1408+127T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 11/19 | chr9 | 101551946 | |||||||
| chr9:101552132 | G | A | 1 | a0001c0001t0008g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1409-9G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 11/19 | chr9 | 101552132 | |||||||
| chr9:101552349 | G | A | 2 | a0001c0007t0001g0045 a0001c0007t0001g0136 |
3 | HG03491.hp2 HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1531-34G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 12/19 | chr9 | 101552349 | |||||||
| chr9:101552896 | C | G | 1 | a0001c0010t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1901+143C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101552896 | |||||||
| chr9:101552973 | G | A | 24 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0017 others(21): Show |
81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1901+220G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101552973 | |||||||
| chr9:101553166 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1901+413C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553166 | |||||||
| chr9:101553301 | G | A | 3 | a0001c0006t0001g0038 a0001c0006t0001g0111 a0001c0006t0001g0112 |
4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1901+548G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553301 | |||||||
| chr9:101553413 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1902-575A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553413 | |||||||
| chr9:101553649 | T | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(34): Show |
88 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1902-339T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553649 | |||||||
| chr9:101553725 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1902-263A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553725 | |||||||
| chr9:101553896 | T | C | 1 | a0001c0002t0001g0098 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1902-92T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553896 | |||||||
| chr9:101554248 | A | T | 1 | a0001c0001t0001g0039 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2019+143A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554248 | |||||||
| chr9:101554311 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2019+206A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554311 | |||||||
| chr9:101554424 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2020-270A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554424 | |||||||
| chr9:101554557 | G | A | 2 | a0001c0002t0001g0032 a0001c0002t0001g0099 |
3 | HG01069.hp1 HG01071.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2020-137G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554557 | |||||||
| chr9:101554570 | C | T | 3 | a0001c0006t0001g0038 a0001c0006t0001g0111 a0001c0006t0001g0112 |
4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2020-124C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554570 | |||||||
| chr9:101554617 | A | G | 1 | a0001c0003t0001g0040 | 2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2020-77A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554617 | |||||||
| chr9:101554670 | T | A | 5 | a0001c0001t0006g0119 a0001c0001t0006g0121 a0001c0004t0002g0006 others(2): Show |
20 | HG00280.hp2 HG01081.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.2020-24T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554670 | |||||||
| chr9:101554893 | A | T | 1 | a0001c0002t0001g0100 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2169+50A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101554893 | |||||||
| chr9:101555024 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2169+181T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555024 | |||||||
| chr9:101555348 | T | A | 1 | a0001c0004t0002g0012 | 5 | HG02080.hp1 HG02129.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.2169+505T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555348 | |||||||
| chr9:101555384 | A | T | 1 | a0001c0003t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2169+541A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555384 | |||||||
| chr9:101555454 | A | G | 12 | a0001c0003t0001g0007 a0001c0003t0001g0010 a0001c0003t0001g0142 others(9): Show |
26 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.2169+611A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555454 | |||||||
| chr9:101555476 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2169+633A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555476 | |||||||
| chr9:101555757 | G | C | 1 | a0001c0001t0001g0028 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2169+914G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555757 | |||||||
| chr9:101555761 | G | A | 1 | a0001c0003t0001g0142 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2169+918G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555761 | |||||||
| chr9:101555789 | T | TA | 8 | a0001c0001t0001g0070 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
10 | HG01261.hp2 HG03098.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.2169+961dupA | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr9 | 101555789 | ||||||
| chr9:101555827 | C | T | 1 | a0001c0011t0007g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2169+984C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555827 | |||||||
| chr9:101555898 | C | T | 3 | a0001c0006t0001g0038 a0001c0006t0001g0111 a0001c0006t0001g0112 |
4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2169+1055C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555898 | |||||||
| chr9:101555997 | T | C | 1 | a0001c0004t0003g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2169+1154T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555997 | |||||||
| chr9:101556005 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0010g0102 |
4 | HG02055.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2169+1162G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556005 | |||||||
| chr9:101556009 | C | CT | 26 | a0001c0001t0001g0083 a0001c0002t0001g0001 a0001c0002t0001g0015 others(23): Show |
83 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.2169+1176dupT | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr9 | 101556009 | ||||||
| chr9:101556276 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2170-1108A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556276 | |||||||
| chr9:101556528 | A | T | 12 | a0001c0003t0001g0007 a0001c0003t0001g0010 a0001c0003t0001g0142 others(9): Show |
26 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.2170-856A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556528 | |||||||
| chr9:101556552 | A | G | 3 | a0001c0006t0001g0038 a0001c0006t0001g0111 a0001c0006t0001g0112 |
4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2170-832A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556552 | |||||||
| chr9:101556610 | A | G | 1 | a0001c0003t0001g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2170-774A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556610 | |||||||
| chr9:101556620 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2170-764G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556620 | |||||||
| chr9:101556691 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2170-693A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556691 | |||||||
| chr9:101556777 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0022 others(78): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.2170-607T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556777 | |||||||
| chr9:101556832 | A | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2170-552A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556832 | |||||||
| chr9:101557042 | T | C | 1 | a0001c0001t0001g0041 | 2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.2170-342T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101557042 | |||||||
| chr9:101557116 | C | T | 1 | a0001c0010t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2170-268C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101557116 | |||||||
| chr9:101557117 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2170-267G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101557117 | |||||||
| chr9:101557648 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2382+52C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101557648 | |||||||
| chr9:101557845 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0072 |
2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.2382+249C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101557845 | |||||||
| chr9:101557867 | G | A | 1 | a0001c0001t0001g0014 | 5 | HG01081.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2382+271G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101557867 | |||||||
| chr9:101557958 | G | T | 5 | a0001c0001t0006g0119 a0001c0001t0006g0121 a0001c0004t0002g0006 others(2): Show |
20 | HG00280.hp2 HG01081.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.2382+362G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101557958 | |||||||
| chr9:101558006 | CT | C | 23 | a0001c0001t0001g0016 a0001c0001t0001g0055 a0001c0001t0001g0071 others(20): Show |
47 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.2382+428delT | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 101558006 | ||||||
| chr9:101558032 | C | T | 1 | a0001c0002t0001g0034 | 2 | NA18977.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.2382+436C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558032 | |||||||
| chr9:101558149 | A | G | 9 | a0001c0001t0006g0119 a0001c0001t0006g0121 a0001c0004t0002g0006 others(6): Show |
29 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.2382+553A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558149 | |||||||
| chr9:101558150 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2382+554T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558150 | |||||||
| chr9:101558152 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2382+556G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558152 | |||||||
| chr9:101558211 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0122 a0001c0001t0001g0125 others(3): Show |
7 | HG02258.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2382+615G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558211 | |||||||
| chr9:101558381 | G | A | 7 | a0001c0003t0001g0007 a0001c0003t0001g0142 a0001c0003t0001g0143 others(4): Show |
15 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.2382+785G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558381 | |||||||
| chr9:101558394 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2382+798G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558394 | |||||||
| chr9:101558414 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2382+818A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558414 | |||||||
| chr9:101558565 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2382+969C>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558565 | |||||||
| chr9:101558726 | T | C | 1 | a0001c0011t0007g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2382+1130T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558726 | |||||||
| chr9:101558936 | G | A | 24 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0017 others(21): Show |
81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.2382+1340G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558936 | |||||||
| chr9:101558950 | G | A | 5 | a0001c0003t0001g0010 a0001c0003t0001g0147 a0001c0003t0001g0148 others(2): Show |
11 | HG02451.hp1 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2382+1354G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558950 | |||||||
| chr9:101559141 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0082 |
8 | HG01952.hp2 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2382+1545A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101559141 | |||||||
| chr9:101559154 | G | T | 1 | a0001c0001t0001g0039 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2382+1558G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101559154 | |||||||
| chr9:101559324 | G | A | 1 | a0001c0007t0001g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2383-1477G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101559324 | |||||||
| chr9:101560524 | T | A | 1 | a0001c0002t0001g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2383-277T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101560524 | |||||||
| chr9:101560672 | A | T | 1 | a0001c0003t0001g0134 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2383-129A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101560672 | |||||||
| chr9:101561360 | A | G | 1 | a0001c0004t0002g0052 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2649+130A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 18/19 | chr9 | 101561360 | |||||||
| chr9:101562214 | G | A | 1 | a0001c0010t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2752-32G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 19/19 | chr9 | 101562214 |