Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6047 |
| ensemblid | ENSG00000063978.17 |
| hgncid | 10067 |
| symbol | RNF4 |
| name | ring finger protein 4 |
| refseq_nuc | NM_002938.5 |
| refseq_prot | NP_002929.1 |
| ensembl_nuc | ENST00000314289.13 |
| ensembl_prot | ENSP00000315212.8 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 2469106 |
| end | 2515857 |
| strand | + |
| ver | v1.2 |
| region | chr4:2469106-2515857 |
| region5000 | chr4:2464106-2520857 |
| regionname0 | RNF4_chr4_2469106_2515857 |
| regionname5000 | RNF4_chr4_2464106_2520857 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 190 | 376 | 92 | 64 | 156 | 18 | 44 | 114 | RNF4_chr4_2464106_2520857 | RNF4 | MSTRK others(185): Show |
chr4 | 2464106 | 2520857 |
| a0002 | 0/0 | 190 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | MSTRK others(185): Show |
chr4 | 2464106 | 2520857 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 570 | 366 | 87 | 60 | 156 | 18 | 43 | RNF4_chr4_2464106_2520857 | RNF4 | ATGAG others(565): Show |
chr4 | 2464106 | 2520857 | ||
| a0001c0002 | 0/0 | 570 | 6 | 4 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | ATGAG others(565): Show |
chr4 | 2464106 | 2520857 | ||
| a0001c0003 | 0/0 | 570 | 3 | 1 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | ATGAG others(565): Show |
chr4 | 2464106 | 2520857 | ||
| a0001c0005 | 0/0 | 570 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | ATGAG others(565): Show |
chr4 | 2464106 | 2520857 | ||
| a0002c0004 | 0/0 | 570 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | ATGAG others(565): Show |
chr4 | 2464106 | 2520857 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2920 | 166 | 27 | 37 | 72 | 8 | 22 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0002 | 0/1 | 2920 | 54 | 3 | 15 | 23 | 6 | 6 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0003 | 0/0 | 2921 | 35 | 9 | 2 | 21 | 1 | 2 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2916): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0004 | 0/0 | 2921 | 22 | 3 | 0 | 18 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2916): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0005 | 0/0 | 2920 | 14 | 2 | 4 | 2 | 0 | 6 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0006 | 0/0 | 2918 | 14 | 14 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2913): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0007 | 1/0 | 2921 | 13 | 7 | 0 | 2 | 0 | 3 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2916): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0008 | 0/0 | 2920 | 10 | 0 | 0 | 10 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0009 | 0/0 | 2921 | 6 | 6 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2916): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0010 | 0/0 | 2920 | 5 | 3 | 0 | 1 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0011 | 0/0 | 2920 | 4 | 4 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0012 | 0/0 | 2921 | 3 | 0 | 0 | 0 | 1 | 2 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2916): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0013 | 0/0 | 2920 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0015 | 0/0 | 2920 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0016 | 0/0 | 2918 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2913): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0017 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0018 | 0/0 | 2920 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0019 | 0/0 | 2920 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0020 | 0/0 | 2920 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0022 | 0/0 | 2921 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2916): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0023 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0024 | 0/0 | 2920 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0025 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0026 | 0/0 | 2920 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0027 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0028 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0029 | 0/0 | 2920 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0030 | 0/0 | 2921 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2916): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0031 | 0/0 | 2921 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2916): Show |
chr4 | 2464106 | 2520857 |
| a0001c0001t0032 | 0/0 | 2920 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0002t0003 | 0/0 | 2921 | 6 | 4 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2916): Show |
chr4 | 2464106 | 2520857 |
| a0001c0003t0014 | 0/0 | 2920 | 2 | 1 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0003t0021 | 0/0 | 2920 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0001c0005t0001 | 0/0 | 2920 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| a0002c0004t0001 | 0/0 | 2920 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | AGCGG others(2915): Show |
chr4 | 2464106 | 2520857 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0319 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0007g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0008g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0010g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0011g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0011g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0011g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0011g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0012g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0012g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0012g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0013g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0013g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0015g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0015g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0017g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0019g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0020g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0022g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0023g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0024g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0025g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0026g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0027g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0028g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0029g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0030g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0031g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0001t0032g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0002t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0002t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0002t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0002t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0003t0014g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0003t0014g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0003t0021g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0001c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0002c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| a0002c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00140 | hp1 | a0001 | c0001 | t0024 | g0215 | EUR | GBR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0190 | EUR | FIN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0265 | EUR | FIN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0216 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00544 | hp2 | a0001 | c0001 | t0008 | g0282 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00609 | hp2 | a0001 | c0001 | t0008 | g0327 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01167 | hp2 | a0001 | c0003 | t0021 | g0306 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0217 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01243 | hp2 | a0001 | c0003 | t0014 | g0370 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0254 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01255 | hp2 | a0001 | c0001 | t0019 | g0087 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01496 | hp1 | a0001 | c0001 | t0026 | g0081 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01515 | hp2 | a0001 | c0001 | t0010 | g0253 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01516 | hp1 | a0001 | c0001 | t0012 | g0247 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0191 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0236 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0234 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02071 | hp2 | a0001 | c0001 | t0027 | g0123 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02129 | hp2 | a0001 | c0001 | t0022 | g0045 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02132 | hp2 | a0001 | c0001 | t0017 | g0009 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0326 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02155 | hp2 | a0001 | c0001 | t0023 | g0023 | EAS | CDX | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | CDX | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0364 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0308 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0249 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02523 | hp1 | a0001 | c0001 | t0007 | g0303 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02630 | hp2 | a0001 | c0001 | t0020 | g0269 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02647 | hp1 | a0001 | c0003 | t0014 | g0357 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02698 | hp2 | a0001 | c0001 | t0018 | g0010 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0227 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0232 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0312 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0016 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0369 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0330 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0162 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0329 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0356 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0352 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03041 | hp2 | a0001 | c0001 | t0016 | g0158 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0350 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0233 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0223 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0351 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03209 | hp2 | a0001 | c0001 | t0029 | g0363 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0368 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0334 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03453 | hp1 | a0002 | c0004 | t0001 | g0057 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0222 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0296 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0297 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0366 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0226 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0021 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0017 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0046 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0018 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03704 | hp1 | a0001 | c0001 | t0012 | g0221 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03831 | hp2 | a0001 | c0001 | t0012 | g0246 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0324 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0325 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18522 | hp2 | a0001 | c0001 | t0032 | g0360 | AFR | YRI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0256 | AFR | YRI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0365 | AFR | YRI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18943 | hp2 | a0001 | c0001 | t0008 | g0322 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18951 | hp2 | a0001 | c0001 | t0008 | g0307 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18952 | hp2 | a0001 | c0001 | t0008 | g0323 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18966 | hp1 | a0001 | c0001 | t0008 | g0321 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18967 | hp2 | a0001 | c0001 | t0025 | g0126 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0333 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19007 | hp2 | a0001 | c0001 | t0008 | g0066 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19011 | hp1 | a0001 | c0001 | t0028 | g0332 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0320 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19030 | hp2 | a0001 | c0002 | t0003 | g0255 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0345 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0305 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19060 | hp2 | a0001 | c0001 | t0030 | g0231 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | ASW | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ASW | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0207 | EUR | TSI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0348 | EUR | TSI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0225 | EUR | TSI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0213 | EUR | TSI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | GIH | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | GIH | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0165 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0245 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG02559 | hp2 | a0001 | c0001 | t0031 | g0228 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0367 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | USA | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | USA | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0328 | AFR | USA | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA20300 | hp2 | a0002 | c0004 | t0001 | g0055 | AFR | USA | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0182 | REF | REF | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0319 | REF | REF | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2469258 | G | A | 1 | a0001 | 1 | HG01255.hp2 | splice_region_variant | LOW | c.-158G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | chr4 | 2469258 | |||||||
| chr4:2512575 | G | A | 1 | a0002 | 2 | HG03453.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.352G>A | p.Asp118Asn | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 6/8 | 662/2921 | 352/573 | 118/190 | chr4 | 2512575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2497042 | A | G | 1 | a0001c0005 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.45A>G | p.Gln15Gln | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/8 | 355/2921 | 45/573 | 15/190 | chr4 | 2497042 | |||
| chr4:2513089 | A | G | 1 | a0001c0003 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
synonymous_variant | LOW | c.381A>G | p.Ser127Ser | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/8 | 691/2921 | 381/573 | 127/190 | chr4 | 2513089 | |||
| chr4:2513119 | C | T | 1 | a0001c0002 | 6 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(3): Show |
synonymous_variant | LOW | c.411C>T | p.Asp137Asp | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/8 | 721/2921 | 411/573 | 137/190 | chr4 | 2513119 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2469147 | A | G | 1 | a0001c0001t0032 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-269A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | 21347 | chr4 | 2469147 | ||||||
| chr4:2469165 | C | G | 7 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(4): Show |
57 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-251C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | 21329 | chr4 | 2469165 | ||||||
| chr4:2469188 | G | A | 1 | a0001c0001t0016 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-228G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | 21306 | chr4 | 2469188 | ||||||
| chr4:2469229 | G | A | 3 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0018 |
16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-187G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | 21265 | chr4 | 2469229 | ||||||
| chr4:2490464 | T | C | 4 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0017 others(1): Show |
18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-30T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/8 | 30 | chr4 | 2490464 | ||||||
| chr4:2513830 | G | A | 1 | a0001c0001t0020 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 11 | chr4 | 2513830 | ||||||
| chr4:2514064 | A | G | 1 | a0001c0001t0029 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 245 | chr4 | 2514064 | ||||||
| chr4:2514166 | G | C | 1 | a0001c0001t0012 | 3 | HG01516.hp1 HG03704.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*347G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 347 | chr4 | 2514166 | ||||||
| chr4:2514268 | G | C | 2 | a0001c0003t0014 a0001c0003t0021 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*449G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 449 | chr4 | 2514268 | ||||||
| chr4:2514395 | ACT | A | 2 | a0001c0001t0006 a0001c0001t0016 |
15 | HG02258.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*579_*580delCT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 579 | INFO_REALIGN_3_PRIME | chr4 | 2514395 | |||||
| chr4:2514465 | C | T | 1 | a0001c0001t0015 | 2 | HG03130.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*646C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 646 | chr4 | 2514465 | ||||||
| chr4:2514543 | C | T | 3 | a0001c0001t0008 a0001c0001t0027 a0001c0001t0028 |
12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*724C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 724 | chr4 | 2514543 | ||||||
| chr4:2514715 | C | G | 1 | a0001c0001t0018 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*896C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 896 | chr4 | 2514715 | ||||||
| chr4:2514720 | G | C | 1 | a0001c0003t0021 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 901 | chr4 | 2514720 | ||||||
| chr4:2514733 | T | C | 1 | a0001c0001t0027 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 914 | chr4 | 2514733 | ||||||
| chr4:2514890 | C | T | 3 | a0001c0001t0008 a0001c0001t0027 a0001c0001t0028 |
12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1071C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1071 | chr4 | 2514890 | ||||||
| chr4:2514979 | G | A | 2 | a0001c0003t0014 a0001c0003t0021 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1160G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1160 | chr4 | 2514979 | ||||||
| chr4:2515031 | C | T | 1 | a0001c0001t0026 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1212 | chr4 | 2515031 | ||||||
| chr4:2515057 | TG | T | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(23): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*1244delG | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1244 | INFO_REALIGN_3_PRIME | chr4 | 2515057 | |||||
| chr4:2515100 | T | G | 1 | a0001c0001t0028 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1281 | chr4 | 2515100 | ||||||
| chr4:2515176 | C | T | 1 | a0001c0001t0017 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1357 | chr4 | 2515176 | ||||||
| chr4:2515270 | C | T | 1 | a0001c0001t0025 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1451 | chr4 | 2515270 | ||||||
| chr4:2515271 | G | A | 1 | a0001c0001t0011 | 4 | HG02257.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1452G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1452 | chr4 | 2515271 | ||||||
| chr4:2515329 | G | A | 1 | a0001c0001t0022 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1510G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1510 | chr4 | 2515329 | ||||||
| chr4:2515340 | T | C | 1 | a0001c0001t0030 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1521T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1521 | chr4 | 2515340 | ||||||
| chr4:2515496 | A | G | 3 | a0001c0001t0002 a0001c0001t0020 a0001c0001t0024 |
55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1677A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1677 | chr4 | 2515496 | ||||||
| chr4:2515511 | G | T | 4 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0027 others(1): Show |
14 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1692G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1692 | chr4 | 2515511 | ||||||
| chr4:2515564 | C | T | 1 | a0001c0001t0009 | 6 | HG01891.hp2 HG02717.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1745C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1745 | chr4 | 2515564 | ||||||
| chr4:2515672 | T | C | 1 | a0001c0001t0024 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1853T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1853 | chr4 | 2515672 | ||||||
| chr4:2515720 | G | A | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
3_prime_UTR_variant | MODIFIER | c.*1901G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1901 | chr4 | 2515720 | ||||||
| chr4:2515751 | T | A | 1 | a0001c0001t0023 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1932T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1932 | chr4 | 2515751 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2469331 | G | C | 1 | a0001c0001t0001g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-158+73G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469331 | |||||||
| chr4:2469387 | A | C | 1 | a0001c0001t0001g0371 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-158+129A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469387 | |||||||
| chr4:2469410 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-158+152G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469410 | |||||||
| chr4:2469463 | A | G | 2 | a0001c0001t0005g0296 a0001c0001t0005g0297 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-158+205A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469463 | |||||||
| chr4:2469476 | G | C | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-158+218G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469476 | |||||||
| chr4:2469490 | C | T | 1 | a0001c0001t0004g0295 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-158+232C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469490 | |||||||
| chr4:2469509 | G | A | 16 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+251G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469509 | |||||||
| chr4:2469742 | G | T | 21 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0353 others(18): Show |
21 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-158+484G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469742 | |||||||
| chr4:2469772 | G | C | 1 | a0001c0001t0001g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-158+514G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469772 | |||||||
| chr4:2469953 | C | A | 1 | a0001c0001t0023g0023 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-158+695C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469953 | |||||||
| chr4:2470075 | A | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-158+817A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470075 | |||||||
| chr4:2470075 | A | T | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-158+817A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470075 | |||||||
| chr4:2470082 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-158+824A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470082 | |||||||
| chr4:2470087 | C | T | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-158+829C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470087 | |||||||
| chr4:2470181 | A | G | 1 | a0001c0001t0004g0292 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-158+923A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470181 | |||||||
| chr4:2470247 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.-158+989T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470247 | |||||||
| chr4:2470352 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-158+1094T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470352 | |||||||
| chr4:2470403 | C | T | 1 | a0001c0001t0003g0291 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-158+1145C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470403 | |||||||
| chr4:2470546 | G | A | 33 | a0001c0001t0001g0150 a0001c0001t0001g0164 a0001c0001t0005g0011 others(30): Show |
33 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.-158+1288G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470546 | |||||||
| chr4:2470599 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+1341A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470599 | |||||||
| chr4:2470633 | A | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0285 others(19): Show |
22 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.-158+1375A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470633 | |||||||
| chr4:2470634 | C | T | 17 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0273 others(14): Show |
17 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.-158+1376C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470634 | |||||||
| chr4:2470694 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG00738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-158+1436G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470694 | |||||||
| chr4:2470756 | G | A | 1 | a0001c0001t0007g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-158+1498G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470756 | |||||||
| chr4:2470827 | CT | C | 189 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0026 others(186): Show |
191 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-158+1580delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2470827 | ||||||
| chr4:2470882 | AAATGCCA others(30): Show |
A | 1 | a0001c0001t0001g0149 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-158+1625_-158+166 others(41): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470882 | |||||||
| chr4:2470943 | T | C | 1 | a0001c0001t0017g0009 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-158+1685T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470943 | |||||||
| chr4:2470962 | CT | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-158+1725delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2470962 | ||||||
| chr4:2470962 | CTT | C | 22 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(19): Show |
22 | HG01109.hp2 HG01243.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.-158+1724_-158+172 others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2470962 | ||||||
| chr4:2471073 | TCTC | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0285 others(19): Show |
22 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.-158+1818_-158+182 others(7): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2471073 | ||||||
| chr4:2471191 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0262 |
3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+1933G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471191 | |||||||
| chr4:2471200 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-158+1942C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471200 | |||||||
| chr4:2471218 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.-158+1960C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471218 | |||||||
| chr4:2471365 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-158+2107A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471365 | |||||||
| chr4:2471460 | C | T | 1 | a0001c0001t0024g0215 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-158+2202C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471460 | |||||||
| chr4:2471460 | CCAGTCAG others(28): Show |
C | 16 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+2211_-158+224 others(39): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2471460 | ||||||
| chr4:2471525 | G | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(318): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-158+2267G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471525 | |||||||
| chr4:2471549 | G | A | 1 | a0001c0001t0010g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-158+2291G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471549 | |||||||
| chr4:2471560 | G | A | 1 | a0001c0001t0005g0011 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-158+2302G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471560 | |||||||
| chr4:2471589 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+2331A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471589 | |||||||
| chr4:2471771 | G | C | 2 | a0001c0001t0003g0271 a0001c0001t0003g0272 |
2 | NA18982.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-158+2513G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471771 | |||||||
| chr4:2472008 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-158+2750A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472008 | |||||||
| chr4:2472131 | T | G | 2 | a0001c0001t0001g0358 a0001c0001t0001g0359 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-158+2873T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472131 | |||||||
| chr4:2472138 | A | C | 1 | a0001c0001t0001g0349 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-158+2880A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472138 | |||||||
| chr4:2472180 | C | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-158+2922C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472180 | |||||||
| chr4:2472197 | A | G | 3 | a0001c0001t0001g0290 a0001c0001t0015g0350 a0001c0001t0015g0351 |
3 | HG02572.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+2939A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472197 | |||||||
| chr4:2472315 | G | C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | NA18964.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-158+3057G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472315 | |||||||
| chr4:2472480 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-158+3222A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472480 | |||||||
| chr4:2472554 | C | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(4): Show |
8 | NA18612.hp1 NA18945.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.-158+3296C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472554 | |||||||
| chr4:2472601 | TA | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.-158+3361delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2472601 | ||||||
| chr4:2472601 | TAA | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0133 others(11): Show |
14 | HG00558.hp1 HG00738.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.-158+3360_-158+336 others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2472601 | ||||||
| chr4:2472601 | TAAAAA | T | 54 | a0001c0001t0001g0140 a0001c0001t0001g0184 a0001c0001t0001g0214 others(51): Show |
55 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.-158+3357_-158+336 others(9): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2472601 | ||||||
| chr4:2472709 | A | T | 17 | a0001c0001t0001g0132 a0001c0001t0005g0011 a0001c0001t0005g0012 others(14): Show |
17 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.-158+3451A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472709 | |||||||
| chr4:2472807 | G | A | 1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-158+3549G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472807 | |||||||
| chr4:2472890 | A | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-158+3632A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472890 | |||||||
| chr4:2472900 | C | A | 1 | a0001c0001t0002g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-158+3642C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472900 | |||||||
| chr4:2472910 | G | T | 2 | a0001c0001t0008g0305 a0001c0001t0008g0345 |
2 | NA19054.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-158+3652G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472910 | |||||||
| chr4:2472912 | C | T | 2 | a0001c0001t0002g0212 a0001c0001t0002g0213 |
2 | HG01934.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-158+3654C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472912 | |||||||
| chr4:2472989 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-158+3731A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472989 | |||||||
| chr4:2473045 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-158+3787A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473045 | |||||||
| chr4:2473046 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-158+3788G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473046 | |||||||
| chr4:2473054 | A | G | 16 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+3796A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473054 | |||||||
| chr4:2473119 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0262 |
3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+3861C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473119 | |||||||
| chr4:2473136 | C | CT | 2 | a0001c0001t0001g0005 a0001c0001t0001g0262 |
3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+3881dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2473136 | ||||||
| chr4:2473179 | T | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-158+3921T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473179 | |||||||
| chr4:2473281 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-158+4023A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473281 | |||||||
| chr4:2473298 | C | T | 51 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0371 others(48): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-158+4040C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473298 | |||||||
| chr4:2473347 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-158+4089G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473347 | |||||||
| chr4:2473381 | T | TA | 18 | a0001c0001t0003g0171 a0001c0001t0003g0257 a0001c0001t0005g0012 others(15): Show |
18 | HG02258.hp2 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-158+4134dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2473381 | ||||||
| chr4:2473381 | T | TC | 3 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG01978.hp1 NA19001.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-158+4123_-158+412 others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473381 | |||||||
| chr4:2473382 | A | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-158+4124A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473382 | |||||||
| chr4:2473403 | C | T | 2 | a0001c0002t0003g0254 a0001c0002t0003g0255 |
2 | HG01255.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-158+4145C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473403 | |||||||
| chr4:2473468 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158+4210A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473468 | |||||||
| chr4:2473473 | A | G | 1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-158+4215A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473473 | |||||||
| chr4:2473629 | GTGAAAC | G | 51 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0371 others(48): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-158+4372_-158+437 others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473629 | |||||||
| chr4:2473639 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-158+4381G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473639 | |||||||
| chr4:2473660 | A | C | 2 | a0001c0001t0001g0343 a0001c0001t0001g0344 |
2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-158+4402A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473660 | |||||||
| chr4:2473822 | G | T | 4 | a0001c0001t0011g0364 a0001c0001t0011g0365 a0001c0001t0011g0366 others(1): Show |
4 | HG02257.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158+4564G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473822 | |||||||
| chr4:2473930 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-158+4672A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473930 | |||||||
| chr4:2474195 | G | T | 2 | a0001c0001t0001g0127 a0001c0001t0025g0126 |
2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-158+4937G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474195 | |||||||
| chr4:2474220 | AC | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-158+4963delC | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474220 | |||||||
| chr4:2474318 | C | T | 11 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0337 others(8): Show |
11 | HG00438.hp1 HG00597.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.-158+5060C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474318 | |||||||
| chr4:2474327 | G | A | 3 | a0001c0001t0001g0290 a0001c0001t0015g0350 a0001c0001t0015g0351 |
3 | HG02572.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+5069G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474327 | |||||||
| chr4:2474381 | C | CA | 20 | a0001c0001t0001g0027 a0001c0001t0001g0049 a0001c0001t0001g0050 others(17): Show |
21 | HG01074.hp1 HG01081.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.-158+5142dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2474381 | ||||||
| chr4:2474381 | CA | C | 164 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0035 others(161): Show |
166 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.-158+5142delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2474381 | ||||||
| chr4:2474381 | CAA | C | 6 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0002g0169 others(3): Show |
6 | HG02145.hp1 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-158+5141_-158+514 others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2474381 | ||||||
| chr4:2474598 | G | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-158+5340G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474598 | |||||||
| chr4:2474752 | C | T | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+5494C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474752 | |||||||
| chr4:2474843 | G | A | 20 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0353 others(17): Show |
20 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-158+5585G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474843 | |||||||
| chr4:2474859 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-158+5601G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474859 | |||||||
| chr4:2474860 | A | C | 51 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0371 others(48): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-158+5602A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474860 | |||||||
| chr4:2474919 | C | T | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+5661C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474919 | |||||||
| chr4:2474983 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-158+5725C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474983 | |||||||
| chr4:2475052 | A | G | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+5794A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475052 | |||||||
| chr4:2475075 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+5817C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475075 | |||||||
| chr4:2475102 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+5844C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475102 | |||||||
| chr4:2475162 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-158+5904A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475162 | |||||||
| chr4:2475168 | A | G | 16 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+5910A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475168 | |||||||
| chr4:2475195 | T | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-158+5937T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475195 | |||||||
| chr4:2475214 | G | A | 1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-158+5956G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475214 | |||||||
| chr4:2475310 | C | T | 2 | a0001c0001t0005g0296 a0001c0001t0005g0297 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-158+6052C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475310 | |||||||
| chr4:2475331 | T | TTTTG | 50 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0371 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.-158+6093_-158+609 others(8): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2475331 | ||||||
| chr4:2475443 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-158+6185A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475443 | |||||||
| chr4:2475501 | G | A | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+6243G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475501 | |||||||
| chr4:2475554 | G | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.-158+6296G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475554 | |||||||
| chr4:2475618 | G | A | 2 | a0001c0001t0003g0218 a0001c0001t0003g0219 |
2 | NA18999.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-158+6360G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475618 | |||||||
| chr4:2476008 | T | C | 1 | a0001c0001t0006g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-158+6750T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476008 | |||||||
| chr4:2476078 | A | G | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-158+6820A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476078 | |||||||
| chr4:2476269 | T | C | 2 | a0001c0001t0002g0058 a0001c0001t0002g0143 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-158+7011T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476269 | |||||||
| chr4:2476533 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-158+7275C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476533 | |||||||
| chr4:2476550 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0262 |
3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+7292G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476550 | |||||||
| chr4:2476586 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-158+7328G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476586 | |||||||
| chr4:2476604 | G | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0262 |
3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+7346G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476604 | |||||||
| chr4:2476642 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-158+7384C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476642 | |||||||
| chr4:2476683 | G | A | 16 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(13): Show |
16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+7425G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476683 | |||||||
| chr4:2476690 | C | G | 1 | a0001c0001t0010g0253 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-158+7432C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476690 | |||||||
| chr4:2476704 | C | CT | 89 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(86): Show |
89 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.-158+7462dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2476704 | ||||||
| chr4:2476704 | CT | C | 15 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0049 others(12): Show |
15 | HG00609.hp1 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-158+7462delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2476704 | ||||||
| chr4:2476707 | T | TC | 5 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-158+7449_-158+745 others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476707 | |||||||
| chr4:2476740 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-158+7482T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476740 | |||||||
| chr4:2476754 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0143 |
2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-158+7496G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476754 | |||||||
| chr4:2476794 | G | A | 54 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0001t0001g0290 others(51): Show |
55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-158+7536G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476794 | |||||||
| chr4:2476812 | C | CT | 18 | a0001c0001t0003g0219 a0001c0001t0005g0011 a0001c0001t0005g0012 others(15): Show |
18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.-158+7568dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2476812 | ||||||
| chr4:2476812 | CT | C | 20 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0064 others(17): Show |
20 | HG01169.hp1 HG01496.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.-158+7568delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2476812 | ||||||
| chr4:2477366 | C | A | 1 | a0001c0001t0002g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-158+8108C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477366 | |||||||
| chr4:2477374 | T | C | 1 | a0001c0001t0008g0066 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-158+8116T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477374 | |||||||
| chr4:2477388 | G | C | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+8130G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477388 | |||||||
| chr4:2477401 | A | G | 17 | a0001c0001t0003g0252 a0001c0001t0005g0011 a0001c0001t0005g0012 others(14): Show |
17 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-158+8143A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477401 | |||||||
| chr4:2477413 | T | C | 88 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0053 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.-158+8155T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477413 | |||||||
| chr4:2477529 | G | A | 4 | a0001c0001t0005g0019 a0001c0001t0006g0154 a0001c0001t0013g0368 others(1): Show |
4 | HG01975.hp2 HG02818.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158+8271G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477529 | |||||||
| chr4:2477575 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-158+8317C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477575 | |||||||
| chr4:2477793 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+8535G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477793 | |||||||
| chr4:2477804 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-158+8546C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477804 | |||||||
| chr4:2477836 | A | G | 1 | a0001c0001t0007g0334 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-158+8578A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477836 | |||||||
| chr4:2477992 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-158+8734G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477992 | |||||||
| chr4:2477993 | A | T | 1 | a0001c0001t0023g0023 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-158+8735A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477993 | |||||||
| chr4:2478033 | A | G | 1 | a0001c0001t0003g0251 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-158+8775A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478033 | |||||||
| chr4:2478086 | T | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(120): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-158+8828T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478086 | |||||||
| chr4:2478284 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-158+9026C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478284 | |||||||
| chr4:2478372 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-158+9114C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478372 | |||||||
| chr4:2478397 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0147 |
2 | HG02056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-158+9139A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478397 | |||||||
| chr4:2478509 | G | T | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-158+9251G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478509 | |||||||
| chr4:2478544 | C | T | 28 | a0001c0001t0002g0122 a0001c0001t0002g0202 a0001c0001t0002g0203 others(25): Show |
29 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.-158+9286C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478544 | |||||||
| chr4:2478550 | A | C | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-158+9292A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478550 | |||||||
| chr4:2478591 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(330): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.-158+9333T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478591 | |||||||
| chr4:2478651 | G | A | 1 | a0001c0002t0003g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-158+9393G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478651 | |||||||
| chr4:2478752 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-158+9494G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478752 | |||||||
| chr4:2478834 | G | A | 4 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158+9576G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478834 | |||||||
| chr4:2478994 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-158+9736G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478994 | |||||||
| chr4:2479352 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-158+10094T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479352 | |||||||
| chr4:2479361 | A | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(117): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-158+10103A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479361 | |||||||
| chr4:2479405 | G | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0285 others(35): Show |
38 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.-158+10147G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479405 | |||||||
| chr4:2479414 | A | T | 3 | a0001c0001t0003g0248 a0001c0001t0003g0250 a0001c0001t0010g0249 |
3 | HG02055.hp1 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-158+10156A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479414 | |||||||
| chr4:2479557 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-158+10299C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479557 | |||||||
| chr4:2479602 | C | G | 1 | a0001c0001t0002g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-158+10344C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479602 | |||||||
| chr4:2479636 | C | T | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-158+10378C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479636 | |||||||
| chr4:2479700 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-158+10442G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479700 | |||||||
| chr4:2479719 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-158+10461G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479719 | |||||||
| chr4:2479746 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-158+10488C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479746 | |||||||
| chr4:2479763 | G | A | 72 | a0001c0001t0003g0170 a0001c0001t0003g0171 a0001c0001t0003g0218 others(69): Show |
72 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-158+10505G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479763 | |||||||
| chr4:2479765 | C | G | 3 | a0001c0001t0012g0221 a0001c0001t0012g0246 a0001c0001t0012g0247 |
3 | HG01516.hp1 HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-158+10507C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479765 | |||||||
| chr4:2479916 | GAGGAGCT others(5): Show |
G | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-157-10419_-157-10 others(18): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2479916 | ||||||
| chr4:2479942 | G | GTCGGTGT others(3): Show |
1 | a0001c0001t0008g0282 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-157-10394_-157-10 others(16): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2479942 | ||||||
| chr4:2480077 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0127 |
2 | NA19007.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-157-10260C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480077 | |||||||
| chr4:2480272 | C | CT | 16 | a0001c0001t0001g0027 a0001c0001t0001g0121 a0001c0001t0001g0130 others(13): Show |
16 | HG01515.hp2 HG01516.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.-157-10047dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2480272 | ||||||
| chr4:2480272 | CT | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0050 others(21): Show |
25 | HG01070.hp1 HG01169.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.-157-10047delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2480272 | ||||||
| chr4:2480297 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-157-10040A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480297 | |||||||
| chr4:2480333 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0029g0363 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-157-10004C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480333 | |||||||
| chr4:2480429 | T | C | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-9908T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480429 | |||||||
| chr4:2480458 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-157-9879A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480458 | |||||||
| chr4:2480524 | T | C | 334 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(331): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-157-9813T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480524 | |||||||
| chr4:2480583 | GA | G | 7 | a0001c0001t0001g0353 a0001c0001t0001g0354 a0001c0001t0001g0355 others(4): Show |
7 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-157-9742delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2480583 | ||||||
| chr4:2480764 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-9573G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480764 | |||||||
| chr4:2480784 | G | A | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-157-9553G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480784 | |||||||
| chr4:2480866 | G | T | 1 | a0001c0001t0010g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-157-9471G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480866 | |||||||
| chr4:2480972 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0002g0174 |
3 | HG03225.hp1 HG04184.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-9365C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480972 | |||||||
| chr4:2481137 | A | G | 1 | a0001c0001t0010g0253 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-157-9200A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481137 | |||||||
| chr4:2481310 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-157-9027A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481310 | |||||||
| chr4:2481419 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-157-8918A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481419 | |||||||
| chr4:2481479 | T | G | 18 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(15): Show |
18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.-157-8858T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481479 | |||||||
| chr4:2481668 | A | G | 6 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-157-8669A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481668 | |||||||
| chr4:2481707 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03490.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-157-8630G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481707 | |||||||
| chr4:2481959 | G | A | 1 | a0001c0001t0007g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-157-8378G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481959 | |||||||
| chr4:2481983 | C | T | 3 | a0001c0003t0014g0357 a0001c0003t0014g0370 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-8354C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481983 | |||||||
| chr4:2482127 | C | G | 35 | a0001c0001t0003g0171 a0001c0001t0003g0224 a0001c0001t0003g0242 others(32): Show |
35 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-157-8210C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482127 | |||||||
| chr4:2482173 | C | A | 1 | a0001c0001t0024g0215 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-157-8164C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482173 | |||||||
| chr4:2482190 | G | A | 2 | a0001c0001t0001g0262 a0001c0001t0029g0363 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-157-8147G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482190 | |||||||
| chr4:2482443 | C | G | 19 | a0001c0001t0001g0005 a0001c0001t0005g0011 a0001c0001t0005g0012 others(16): Show |
20 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-157-7894C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482443 | |||||||
| chr4:2482476 | C | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0285 others(35): Show |
38 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.-157-7861C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482476 | |||||||
| chr4:2482480 | G | A | 1 | a0001c0003t0014g0357 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-157-7857G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482480 | |||||||
| chr4:2482481 | G | T | 1 | a0001c0003t0014g0357 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-157-7856G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482481 | |||||||
| chr4:2482668 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-157-7669T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482668 | |||||||
| chr4:2482849 | GCCTGT | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-157-7486_-157-748 others(9): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2482849 | ||||||
| chr4:2482916 | G | T | 18 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(15): Show |
18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.-157-7421G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482916 | |||||||
| chr4:2482931 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-7406C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482931 | |||||||
| chr4:2482984 | T | C | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-157-7353T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482984 | |||||||
| chr4:2483130 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-157-7207T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483130 | |||||||
| chr4:2483328 | T | C | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-7009T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483328 | |||||||
| chr4:2483364 | A | C | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6973A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483364 | |||||||
| chr4:2483370 | G | C | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6967G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483370 | |||||||
| chr4:2483371 | T | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6966T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483371 | |||||||
| chr4:2483568 | T | C | 337 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(334): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-157-6769T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483568 | |||||||
| chr4:2483578 | C | G | 1 | a0001c0001t0002g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-157-6759C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483578 | |||||||
| chr4:2483660 | C | T | 94 | a0001c0001t0003g0171 a0001c0001t0003g0218 a0001c0001t0003g0219 others(91): Show |
95 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-157-6677C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483660 | |||||||
| chr4:2483675 | G | A | 1 | a0001c0001t0003g0225 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-157-6662G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483675 | |||||||
| chr4:2483850 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-157-6487T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483850 | |||||||
| chr4:2483888 | A | C | 50 | a0001c0001t0002g0004 a0001c0001t0002g0122 a0001c0001t0002g0167 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.-157-6449A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483888 | |||||||
| chr4:2483895 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-6442C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483895 | |||||||
| chr4:2483901 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0029g0363 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-157-6436C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483901 | |||||||
| chr4:2483946 | G | C | 4 | a0001c0001t0020g0269 a0001c0003t0014g0357 a0001c0003t0014g0370 others(1): Show |
4 | HG01167.hp2 HG01243.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157-6391G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483946 | |||||||
| chr4:2483949 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-157-6388C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483949 | |||||||
| chr4:2483971 | C | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0285 others(35): Show |
38 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.-157-6366C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483971 | |||||||
| chr4:2483983 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6354C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483983 | |||||||
| chr4:2484042 | G | A | 1 | a0001c0001t0003g0267 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-157-6295G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484042 | |||||||
| chr4:2484047 | G | A | 1 | a0001c0001t0032g0360 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-157-6290G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484047 | |||||||
| chr4:2484067 | T | TCCCCC | 15 | a0001c0001t0001g0318 a0001c0001t0001g0358 a0001c0001t0001g0359 others(12): Show |
16 | HG00544.hp1 HG00544.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157-6266_-157-626 others(9): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCC | 25 | a0001c0001t0001g0115 a0001c0001t0001g0132 a0001c0001t0001g0144 others(22): Show |
25 | HG00408.hp2 HG01257.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-157-6267_-157-626 others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(1): Show |
17 | a0001c0001t0001g0039 a0001c0001t0001g0083 a0001c0001t0001g0125 others(14): Show |
17 | HG00735.hp1 HG01106.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.-157-6269_-157-626 others(12): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(9): Show |
1 | a0001c0001t0003g0259 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(20): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(3): Show |
2 | a0001c0001t0001g0300 a0001c0001t0006g0154 |
2 | HG03540.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(14): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(4): Show |
11 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0114 others(8): Show |
12 | HG00438.hp1 HG00639.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(15): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(5): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0079 a0001c0001t0001g0110 others(10): Show |
14 | HG00140.hp2 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(16): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(6): Show |
16 | a0001c0001t0001g0047 a0001c0001t0001g0069 a0001c0001t0001g0073 others(13): Show |
16 | HG00280.hp1 HG01257.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(17): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(7): Show |
14 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0052 others(11): Show |
15 | HG00099.hp1 HG00741.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(18): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(8): Show |
16 | a0001c0001t0001g0032 a0001c0001t0001g0061 a0001c0001t0001g0062 others(13): Show |
16 | HG00438.hp2 HG00609.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(19): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(9): Show |
33 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0035 others(30): Show |
33 | HG00558.hp1 HG00738.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(20): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(10): Show |
24 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0064 others(21): Show |
24 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(21): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(11): Show |
23 | a0001c0001t0001g0027 a0001c0001t0001g0037 a0001c0001t0001g0093 others(20): Show |
23 | HG00099.hp2 HG00408.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(22): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(12): Show |
18 | a0001c0001t0001g0036 a0001c0001t0001g0091 a0001c0001t0001g0092 others(15): Show |
18 | HG00609.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(23): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(13): Show |
19 | a0001c0001t0001g0051 a0001c0001t0001g0089 a0001c0001t0001g0090 others(16): Show |
19 | HG00140.hp1 HG00280.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(24): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(14): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0088 others(7): Show |
11 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(25): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(15): Show |
15 | a0001c0001t0001g0028 a0001c0001t0001g0347 a0001c0001t0002g0189 others(12): Show |
16 | HG00642.hp1 HG01099.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(26): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(16): Show |
9 | a0001c0001t0001g0060 a0001c0001t0001g0085 a0001c0001t0001g0353 others(6): Show |
9 | HG02056.hp1 HG02083.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(27): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(17): Show |
8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0002g0175 others(5): Show |
8 | HG00673.hp1 HG01169.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(28): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(18): Show |
5 | a0001c0001t0002g0264 a0001c0001t0003g0248 a0001c0001t0004g0084 others(2): Show |
5 | HG02809.hp1 HG03195.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(29): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(19): Show |
2 | a0001c0001t0001g0348 a0001c0001t0002g0187 |
2 | NA18968.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(30): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(20): Show |
2 | a0001c0001t0002g0186 a0001c0001t0002g0210 |
2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(31): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(21): Show |
1 | a0001c0005t0001g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(32): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(23): Show |
1 | a0001c0001t0004g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(34): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCCC others(28): Show |
1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(39): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TCCCCCGC others(8): Show |
1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-157-6265_-157-626 others(19): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | ||||||
| chr4:2484067 | T | TTCCCCCC others(4): Show |
1 | a0001c0001t0004g0292 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-157-6270_-157-626 others(15): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484067 | |||||||
| chr4:2484067 | T | TTCCCCCC others(10): Show |
1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-157-6270_-157-626 others(21): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484067 | |||||||
| chr4:2484068 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6269C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484068 | |||||||
| chr4:2484071 | C | CCCCCCCC others(6): Show |
1 | a0001c0001t0001g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(17): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484071 | ||||||
| chr4:2484071 | C | CCCCCCCC others(5): Show |
3 | a0001c0001t0001g0075 a0001c0001t0002g0058 a0001c0001t0002g0143 |
3 | HG00642.hp2 HG00735.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(16): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484071 | ||||||
| chr4:2484071 | C | CCCCG | 19 | a0001c0001t0001g0005 a0001c0001t0005g0011 a0001c0001t0005g0012 others(16): Show |
20 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-157-6263_-157-626 others(8): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484071 | ||||||
| chr4:2484074 | C | CCCCCCCC others(9): Show |
1 | a0001c0001t0001g0059 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(20): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484074 | ||||||
| chr4:2484076 | G | C | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6261G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484076 | |||||||
| chr4:2484080 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-157-6257C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484080 | |||||||
| chr4:2484094 | G | T | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-6243G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484094 | |||||||
| chr4:2484205 | T | C | 1 | a0001c0001t0010g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-157-6132T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484205 | |||||||
| chr4:2484513 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-157-5824A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484513 | |||||||
| chr4:2484576 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-157-5761A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484576 | |||||||
| chr4:2484589 | A | G | 1 | a0001c0001t0002g0205 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-157-5748A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484589 | |||||||
| chr4:2484599 | A | G | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-5738A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484599 | |||||||
| chr4:2484759 | C | T | 95 | a0001c0001t0003g0170 a0001c0001t0003g0171 a0001c0001t0003g0218 others(92): Show |
96 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-157-5578C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484759 | |||||||
| chr4:2484798 | G | A | 1 | a0001c0003t0014g0357 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-157-5539G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484798 | |||||||
| chr4:2484877 | C | G | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-157-5460C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484877 | |||||||
| chr4:2484894 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-157-5443A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484894 | |||||||
| chr4:2484974 | G | T | 2 | a0001c0001t0002g0190 a0001c0001t0002g0265 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-157-5363G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484974 | |||||||
| chr4:2485174 | C | T | 1 | a0001c0001t0008g0345 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-157-5163C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485174 | |||||||
| chr4:2485358 | A | C | 1 | a0001c0003t0014g0357 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-157-4979A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485358 | |||||||
| chr4:2485377 | A | G | 1 | a0001c0001t0004g0033 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-157-4960A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485377 | |||||||
| chr4:2485424 | C | G | 6 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0011g0364 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-157-4913C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485424 | |||||||
| chr4:2485593 | A | G | 1 | a0001c0001t0009g0232 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-157-4744A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485593 | |||||||
| chr4:2485639 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.-157-4698C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485639 | |||||||
| chr4:2485698 | C | A | 1 | a0001c0001t0003g0170 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-157-4639C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485698 | |||||||
| chr4:2485780 | G | A | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-4557G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485780 | |||||||
| chr4:2485850 | G | A | 14 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0044 others(11): Show |
14 | HG02004.hp2 NA18612.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.-157-4487G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485850 | |||||||
| chr4:2485919 | T | G | 1 | a0001c0001t0002g0176 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-157-4418T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485919 | |||||||
| chr4:2485994 | G | A | 1 | a0001c0001t0006g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-157-4343G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485994 | |||||||
| chr4:2486703 | A | C | 1 | a0001c0001t0002g0120 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-157-3634A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486703 | |||||||
| chr4:2486704 | G | C | 1 | a0001c0001t0002g0120 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-157-3633G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486704 | |||||||
| chr4:2486761 | C | T | 91 | a0001c0001t0003g0171 a0001c0001t0003g0218 a0001c0001t0003g0219 others(88): Show |
92 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.-157-3576C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486761 | |||||||
| chr4:2486868 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-157-3469C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486868 | |||||||
| chr4:2486982 | G | A | 91 | a0001c0001t0003g0171 a0001c0001t0003g0218 a0001c0001t0003g0219 others(88): Show |
92 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.-157-3355G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486982 | |||||||
| chr4:2487069 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-157-3268G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487069 | |||||||
| chr4:2487113 | C | A | 1 | a0001c0001t0017g0009 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-157-3224C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487113 | |||||||
| chr4:2487216 | C | G | 1 | a0001c0001t0002g0181 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-157-3121C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487216 | |||||||
| chr4:2487280 | A | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0285 others(29): Show |
32 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.-157-3057A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487280 | |||||||
| chr4:2487430 | C | T | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-157-2907C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487430 | |||||||
| chr4:2487651 | G | A | 2 | a0001c0001t0009g0226 a0001c0001t0009g0232 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-157-2686G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487651 | |||||||
| chr4:2487804 | T | C | 1 | a0001c0001t0001g0358 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-157-2533T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487804 | |||||||
| chr4:2487866 | A | G | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-2471A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487866 | |||||||
| chr4:2487905 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-157-2432C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487905 | |||||||
| chr4:2488022 | C | T | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-2315C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488022 | |||||||
| chr4:2488072 | C | T | 3 | a0001c0001t0001g0262 a0001c0001t0015g0350 a0001c0001t0015g0351 |
3 | HG01884.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-157-2265C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488072 | |||||||
| chr4:2488106 | G | A | 2 | a0001c0001t0008g0066 a0001c0001t0008g0327 |
2 | HG00609.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-157-2231G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488106 | |||||||
| chr4:2488229 | G | A | 1 | a0001c0001t0003g0260 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-157-2108G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488229 | |||||||
| chr4:2488371 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-157-1966G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488371 | |||||||
| chr4:2488375 | A | C | 1 | a0001c0001t0001g0337 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-157-1962A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488375 | |||||||
| chr4:2488473 | C | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0074 a0001c0001t0001g0150 others(19): Show |
23 | HG01261.hp1 HG02258.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.-157-1864C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488473 | |||||||
| chr4:2488476 | A | C | 4 | a0001c0001t0001g0071 a0001c0003t0014g0357 a0001c0003t0014g0370 others(1): Show |
4 | HG01167.hp2 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157-1861A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488476 | |||||||
| chr4:2488518 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-157-1819C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488518 | |||||||
| chr4:2488548 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(114): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.-157-1789G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488548 | |||||||
| chr4:2488757 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-1580C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488757 | |||||||
| chr4:2488809 | A | ATTAT | 59 | a0001c0001t0001g0053 a0001c0001t0001g0077 a0001c0001t0001g0097 others(56): Show |
60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.-157-1526_-157-152 others(8): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2488809 | ||||||
| chr4:2488812 | T | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-157-1525T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488812 | |||||||
| chr4:2488824 | A | T | 93 | a0001c0001t0001g0008 a0001c0001t0003g0171 a0001c0001t0003g0218 others(90): Show |
94 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-157-1513A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488824 | |||||||
| chr4:2488855 | G | A | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-1482G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488855 | |||||||
| chr4:2488888 | G | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-1449G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488888 | |||||||
| chr4:2488971 | A | C | 335 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(332): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-157-1366A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488971 | |||||||
| chr4:2488991 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-157-1346C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488991 | |||||||
| chr4:2489040 | T | G | 21 | a0001c0001t0001g0164 a0001c0001t0001g0285 a0001c0001t0001g0286 others(18): Show |
21 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-157-1297T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489040 | |||||||
| chr4:2489053 | T | TC | 24 | a0001c0001t0007g0006 a0001c0001t0007g0303 a0001c0001t0007g0308 others(21): Show |
25 | HG00544.hp2 HG00609.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-157-1282dupC | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2489053 | ||||||
| chr4:2489113 | G | A | 1 | a0001c0001t0032g0360 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-157-1224G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489113 | |||||||
| chr4:2489184 | C | T | 1 | a0001c0002t0003g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-157-1153C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489184 | |||||||
| chr4:2489233 | T | G | 1 | a0001c0001t0003g0259 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-157-1104T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489233 | |||||||
| chr4:2489247 | C | G | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-1090C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489247 | |||||||
| chr4:2489280 | A | T | 1 | a0001c0001t0002g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-157-1057A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489280 | |||||||
| chr4:2489417 | T | A | 1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-157-920T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489417 | |||||||
| chr4:2489420 | G | T | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-917G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489420 | |||||||
| chr4:2489422 | C | G | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-915C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489422 | |||||||
| chr4:2489488 | A | G | 94 | a0001c0001t0001g0008 a0001c0001t0003g0170 a0001c0001t0003g0171 others(91): Show |
95 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-157-849A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489488 | |||||||
| chr4:2489556 | G | A | 2 | a0001c0001t0005g0013 a0001c0001t0005g0014 |
2 | HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-157-781G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489556 | |||||||
| chr4:2489701 | A | G | 1 | a0001c0001t0006g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-157-636A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489701 | |||||||
| chr4:2489762 | A | G | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-575A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489762 | |||||||
| chr4:2489794 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-157-543C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489794 | |||||||
| chr4:2489827 | C | G | 1 | a0001c0001t0002g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-157-510C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489827 | |||||||
| chr4:2489832 | C | T | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-505C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489832 | |||||||
| chr4:2489948 | A | G | 2 | a0001c0001t0002g0185 a0001c0001t0002g0199 |
2 | NA18952.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-157-389A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489948 | |||||||
| chr4:2489968 | G | A | 36 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0049 others(33): Show |
36 | HG00140.hp2 HG00609.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.-157-369G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489968 | |||||||
| chr4:2490221 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-116C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2490221 | |||||||
| chr4:2490230 | G | A | 1 | a0001c0001t0007g0324 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-157-107G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2490230 | |||||||
| chr4:2490669 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.9+167C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2490669 | |||||||
| chr4:2491077 | T | TA | 3 | a0001c0003t0014g0357 a0001c0003t0014g0370 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.9+578dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2491077 | ||||||
| chr4:2491090 | A | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+588A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491090 | |||||||
| chr4:2491156 | A | T | 18 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(15): Show |
18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.9+654A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491156 | |||||||
| chr4:2491528 | C | T | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.9+1026C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491528 | |||||||
| chr4:2491589 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.9+1087C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491589 | |||||||
| chr4:2491622 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | NA18951.hp1 NA18977.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+1120A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491622 | |||||||
| chr4:2491765 | A | C | 53 | a0001c0001t0002g0004 a0001c0001t0002g0122 a0001c0001t0002g0167 others(50): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.9+1263A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491765 | |||||||
| chr4:2491791 | T | G | 1 | a0001c0001t0002g0195 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.9+1289T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491791 | |||||||
| chr4:2492061 | A | C | 94 | a0001c0001t0001g0008 a0001c0001t0003g0170 a0001c0001t0003g0171 others(91): Show |
95 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.9+1559A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492061 | |||||||
| chr4:2492237 | G | A | 1 | a0001c0001t0006g0160 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9+1735G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492237 | |||||||
| chr4:2492313 | G | A | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.9+1811G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492313 | |||||||
| chr4:2492458 | G | A | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+1956G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492458 | |||||||
| chr4:2492512 | G | A | 53 | a0001c0001t0002g0004 a0001c0001t0002g0122 a0001c0001t0002g0167 others(50): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.9+2010G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492512 | |||||||
| chr4:2492975 | A | T | 335 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(332): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.9+2473A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492975 | |||||||
| chr4:2492981 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.9+2479G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492981 | |||||||
| chr4:2493180 | C | A | 1 | a0001c0001t0004g0274 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.9+2678C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493180 | |||||||
| chr4:2493221 | G | T | 1 | a0001c0001t0001g0214 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.9+2719G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493221 | |||||||
| chr4:2493300 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.9+2798G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493300 | |||||||
| chr4:2493433 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.9+2931A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493433 | |||||||
| chr4:2493503 | A | G | 2 | a0001c0001t0011g0365 a0001c0001t0011g0366 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+3001A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493503 | |||||||
| chr4:2493743 | T | TA | 12 | a0001c0001t0001g0026 a0001c0001t0001g0048 a0001c0001t0001g0075 others(9): Show |
12 | HG00408.hp1 HG00438.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.10-3242dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2493743 | ||||||
| chr4:2493743 | T | TAA | 50 | a0001c0001t0001g0290 a0001c0001t0002g0004 a0001c0001t0002g0168 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.10-3243_10-3242dup others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2493743 | ||||||
| chr4:2493743 | TA | T | 109 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0088 others(106): Show |
109 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.10-3242delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2493743 | ||||||
| chr4:2493743 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.10-3251_10-3242del others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2493743 | ||||||
| chr4:2493794 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.10-3213C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493794 | |||||||
| chr4:2493998 | A | G | 336 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(333): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.10-3009A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493998 | |||||||
| chr4:2494000 | G | A | 53 | a0001c0001t0002g0004 a0001c0001t0002g0122 a0001c0001t0002g0167 others(50): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.10-3007G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494000 | |||||||
| chr4:2494032 | G | A | 1 | a0001c0002t0003g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10-2975G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494032 | |||||||
| chr4:2494094 | G | A | 2 | a0001c0001t0002g0169 a0001c0001t0002g0194 |
2 | NA18966.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.10-2913G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494094 | |||||||
| chr4:2494110 | T | A | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.10-2897T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494110 | |||||||
| chr4:2494146 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.10-2861A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494146 | |||||||
| chr4:2494165 | G | A | 2 | a0002c0004t0001g0055 a0002c0004t0001g0057 |
2 | HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.10-2842G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494165 | |||||||
| chr4:2494172 | C | T | 338 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(335): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.10-2835C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494172 | |||||||
| chr4:2494194 | A | T | 3 | a0001c0003t0014g0357 a0001c0003t0014g0370 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.10-2813A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494194 | |||||||
| chr4:2494227 | A | G | 1 | a0001c0001t0007g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.10-2780A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494227 | |||||||
| chr4:2494304 | A | G | 335 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(332): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.10-2703A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494304 | |||||||
| chr4:2494351 | C | G | 1 | a0001c0001t0003g0279 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.10-2656C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494351 | |||||||
| chr4:2494373 | C | CT | 61 | a0001c0001t0001g0034 a0001c0001t0001g0289 a0001c0001t0001g0290 others(58): Show |
62 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.10-2614dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2494373 | ||||||
| chr4:2494373 | C | CTT | 8 | a0001c0001t0001g0304 a0001c0001t0002g0167 a0001c0001t0002g0172 others(5): Show |
8 | HG00140.hp1 HG00741.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-2615_10-2614dup others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2494373 | ||||||
| chr4:2494373 | CT | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.10-2614delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2494373 | ||||||
| chr4:2494373 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.10-2624_10-2614del others(11): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2494373 | ||||||
| chr4:2494394 | G | T | 3 | a0001c0003t0014g0357 a0001c0003t0014g0370 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.10-2613G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494394 | |||||||
| chr4:2494416 | G | A | 1 | a0001c0001t0010g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.10-2591G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494416 | |||||||
| chr4:2494570 | T | C | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2437T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494570 | |||||||
| chr4:2494571 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2436G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494571 | |||||||
| chr4:2494571 | G | C | 1 | a0001c0001t0017g0009 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.10-2436G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494571 | |||||||
| chr4:2494579 | T | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2428T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494579 | |||||||
| chr4:2494580 | A | C | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2427A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494580 | |||||||
| chr4:2494582 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2425G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494582 | |||||||
| chr4:2494607 | T | C | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2400T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494607 | |||||||
| chr4:2494622 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0107 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.10-2385C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494622 | |||||||
| chr4:2494623 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2384G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494623 | |||||||
| chr4:2494628 | C | T | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2379C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494628 | |||||||
| chr4:2494634 | C | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2373C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494634 | |||||||
| chr4:2494660 | A | G | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2347A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494660 | |||||||
| chr4:2494662 | G | C | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2345G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494662 | |||||||
| chr4:2494663 | C | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2344C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494663 | |||||||
| chr4:2494817 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.10-2190T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494817 | |||||||
| chr4:2494825 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.10-2182C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494825 | |||||||
| chr4:2495046 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.10-1961A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495046 | |||||||
| chr4:2495086 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.10-1921G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495086 | |||||||
| chr4:2495087 | T | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.10-1920T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495087 | |||||||
| chr4:2495088 | GTCAGCTC others(4): Show |
G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.10-1918_10-1908del others(11): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495088 | |||||||
| chr4:2495168 | C | T | 6 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.10-1839C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495168 | |||||||
| chr4:2495180 | T | A | 1 | a0001c0001t0004g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.10-1827T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495180 | |||||||
| chr4:2495181 | C | T | 1 | a0001c0001t0004g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.10-1826C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495181 | |||||||
| chr4:2495331 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0106 |
2 | HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.10-1676A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495331 | |||||||
| chr4:2495386 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.10-1621C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495386 | |||||||
| chr4:2495426 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.10-1581G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495426 | |||||||
| chr4:2495476 | C | T | 1 | a0001c0001t0007g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.10-1531C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495476 | |||||||
| chr4:2495599 | A | AT | 3 | a0001c0003t0014g0357 a0001c0003t0014g0370 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.10-1407dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2495599 | ||||||
| chr4:2495638 | T | TGG | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0002g0173 others(1): Show |
4 | HG03471.hp2 HG03704.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.10-1369_10-1368ins others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495638 | |||||||
| chr4:2495639 | T | G | 9 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
10 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.10-1368T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495639 | |||||||
| chr4:2495639 | T | TG | 70 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(67): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.10-1359dupG | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2495639 | ||||||
| chr4:2495639 | T | TGG | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.10-1360_10-1359dup others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2495639 | ||||||
| chr4:2495640 | G | T | 3 | a0001c0001t0015g0350 a0001c0001t0015g0351 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.10-1367G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495640 | |||||||
| chr4:2495641 | G | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.10-1366G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495641 | |||||||
| chr4:2495642 | G | A | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.10-1365G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495642 | |||||||
| chr4:2495646 | G | C | 19 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(16): Show |
19 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.10-1361G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495646 | |||||||
| chr4:2495646 | G | T | 8 | a0001c0001t0003g0171 a0001c0001t0003g0243 a0001c0001t0003g0248 others(5): Show |
8 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-1361G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495646 | |||||||
| chr4:2495647 | G | C | 1 | a0001c0001t0007g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.10-1360G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495647 | |||||||
| chr4:2495647 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.10-1360G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495647 | |||||||
| chr4:2496096 | G | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.10-911G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2496096 | |||||||
| chr4:2496371 | T | G | 3 | a0001c0003t0014g0357 a0001c0003t0014g0370 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.10-636T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2496371 | |||||||
| chr4:2496717 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.10-290C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2496717 | |||||||
| chr4:2497201 | T | C | 1 | a0001c0001t0004g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.124+80T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497201 | |||||||
| chr4:2497239 | C | T | 3 | a0001c0001t0007g0006 a0001c0001t0007g0308 a0001c0001t0007g0328 |
4 | HG01891.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+118C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497239 | |||||||
| chr4:2497245 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.124+124A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497245 | |||||||
| chr4:2497356 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.124+235G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497356 | |||||||
| chr4:2497381 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.124+260A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497381 | |||||||
| chr4:2497390 | T | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.124+269T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497390 | |||||||
| chr4:2497431 | C | T | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.124+310C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497431 | |||||||
| chr4:2497624 | T | C | 2 | a0001c0001t0003g0271 a0001c0001t0003g0272 |
2 | NA18982.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.124+503T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497624 | |||||||
| chr4:2497659 | G | C | 3 | a0001c0003t0014g0357 a0001c0003t0014g0370 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.124+538G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497659 | |||||||
| chr4:2497673 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+552C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497673 | |||||||
| chr4:2497881 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.124+760G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497881 | |||||||
| chr4:2497941 | C | G | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.124+820C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497941 | |||||||
| chr4:2498069 | C | G | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.124+948C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498069 | |||||||
| chr4:2498111 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.124+990C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498111 | |||||||
| chr4:2498141 | C | T | 1 | a0001c0001t0007g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.124+1020C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498141 | |||||||
| chr4:2498205 | G | A | 338 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(335): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.124+1084G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498205 | |||||||
| chr4:2498319 | G | A | 1 | a0001c0001t0004g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.124+1198G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498319 | |||||||
| chr4:2498427 | A | G | 2 | a0001c0001t0002g0190 a0001c0001t0002g0265 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.124+1306A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498427 | |||||||
| chr4:2498479 | G | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0289 |
2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.124+1358G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498479 | |||||||
| chr4:2498603 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.124+1482G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498603 | |||||||
| chr4:2498742 | A | C | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.124+1621A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498742 | |||||||
| chr4:2498849 | C | T | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124+1728C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498849 | |||||||
| chr4:2498922 | C | T | 6 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0011g0364 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-1737C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498922 | |||||||
| chr4:2498962 | C | T | 8 | a0001c0001t0001g0029 a0001c0001t0001g0092 a0001c0001t0001g0094 others(5): Show |
8 | HG00408.hp1 HG00558.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-1697C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498962 | |||||||
| chr4:2498968 | G | A | 1 | a0001c0001t0007g0330 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.125-1691G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498968 | |||||||
| chr4:2499070 | G | A | 42 | a0001c0001t0002g0004 a0001c0001t0002g0122 a0001c0001t0002g0167 others(39): Show |
43 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.125-1589G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499070 | |||||||
| chr4:2499173 | G | A | 2 | a0001c0001t0007g0324 a0001c0001t0007g0334 |
2 | HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.125-1486G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499173 | |||||||
| chr4:2499175 | C | T | 1 | a0001c0001t0006g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.125-1484C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499175 | |||||||
| chr4:2499183 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.125-1476C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499183 | |||||||
| chr4:2499308 | T | C | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.125-1351T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499308 | |||||||
| chr4:2499369 | G | A | 1 | a0001c0001t0001g0371 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.125-1290G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499369 | |||||||
| chr4:2499451 | T | G | 1 | a0001c0001t0002g0202 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.125-1208T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499451 | |||||||
| chr4:2499495 | C | T | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.125-1164C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499495 | |||||||
| chr4:2499506 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125-1153C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499506 | |||||||
| chr4:2499518 | C | A | 1 | a0001c0001t0001g0335 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.125-1141C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499518 | |||||||
| chr4:2499588 | TTTAATA | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.125-1058_125-1053d others(8): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 2499588 | ||||||
| chr4:2499632 | C | T | 1 | a0001c0001t0007g0330 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.125-1027C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499632 | |||||||
| chr4:2499667 | G | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.125-992G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499667 | |||||||
| chr4:2499843 | G | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.125-816G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499843 | |||||||
| chr4:2500031 | G | A | 1 | a0001c0001t0010g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.125-628G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500031 | |||||||
| chr4:2500156 | C | CA | 12 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0043 others(9): Show |
13 | HG00280.hp2 HG00323.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.125-482dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 2500156 | ||||||
| chr4:2500156 | CA | C | 126 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0049 others(123): Show |
127 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.125-482delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 2500156 | ||||||
| chr4:2500156 | CAA | C | 6 | a0001c0001t0001g0039 a0001c0001t0015g0350 a0001c0001t0015g0351 others(3): Show |
6 | HG01167.hp2 HG01243.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-483_125-482del others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 2500156 | ||||||
| chr4:2500197 | C | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0199 |
2 | NA18952.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.125-462C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500197 | |||||||
| chr4:2500207 | A | C | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.125-452A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500207 | |||||||
| chr4:2500274 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.125-385G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500274 | |||||||
| chr4:2500301 | A | T | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.125-358A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500301 | |||||||
| chr4:2500421 | C | A | 1 | a0001c0001t0005g0012 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.125-238C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500421 | |||||||
| chr4:2500457 | C | T | 1 | a0001c0001t0009g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.125-202C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500457 | |||||||
| chr4:2500469 | T | A | 1 | a0001c0001t0005g0011 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.125-190T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500469 | |||||||
| chr4:2500497 | T | A | 1 | a0001c0001t0005g0012 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.125-162T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500497 | |||||||
| chr4:2500514 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.125-145G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500514 | |||||||
| chr4:2500572 | A | ATT | 336 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(333): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.125-87_125-86insTT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500572 | |||||||
| chr4:2500777 | A | G | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+39A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2500777 | |||||||
| chr4:2500791 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.204+53A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2500791 | |||||||
| chr4:2500910 | T | C | 97 | a0001c0001t0001g0008 a0001c0001t0003g0170 a0001c0001t0003g0171 others(94): Show |
98 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.204+172T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2500910 | |||||||
| chr4:2501078 | G | C | 1 | a0001c0001t0002g0180 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.204+340G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501078 | |||||||
| chr4:2501108 | C | T | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | HG03831.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.204+370C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501108 | |||||||
| chr4:2501206 | C | T | 1 | a0002c0004t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.204+468C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501206 | |||||||
| chr4:2501415 | G | GGGAGGCT others(8): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+686_204+700dup others(15): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2501415 | ||||||
| chr4:2501562 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+824C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501562 | |||||||
| chr4:2501577 | T | C | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+839T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501577 | |||||||
| chr4:2501615 | T | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+877T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501615 | |||||||
| chr4:2501667 | C | G | 1 | a0001c0001t0002g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.204+929C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501667 | |||||||
| chr4:2501735 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.204+997G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501735 | |||||||
| chr4:2501766 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+1028C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501766 | |||||||
| chr4:2501860 | T | C | 8 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0210 others(5): Show |
8 | HG00639.hp1 HG02004.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+1122T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501860 | |||||||
| chr4:2501877 | G | A | 1 | a0001c0001t0003g0235 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.204+1139G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501877 | |||||||
| chr4:2501909 | C | A | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.204+1171C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501909 | |||||||
| chr4:2502108 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.204+1370C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502108 | |||||||
| chr4:2502195 | A | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02015.hp1 HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.204+1457A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502195 | |||||||
| chr4:2502240 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.204+1502T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502240 | |||||||
| chr4:2502468 | A | G | 117 | a0001c0001t0003g0170 a0001c0001t0003g0171 a0001c0001t0003g0218 others(114): Show |
118 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.204+1730A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502468 | |||||||
| chr4:2502562 | T | C | 3 | a0001c0003t0014g0357 a0001c0003t0014g0370 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+1824T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502562 | |||||||
| chr4:2502630 | T | C | 337 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(334): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.204+1892T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502630 | |||||||
| chr4:2502671 | C | CA | 15 | a0001c0001t0001g0047 a0001c0001t0001g0124 a0001c0001t0001g0353 others(12): Show |
15 | HG02135.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.204+1948dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2502671 | ||||||
| chr4:2502843 | C | CA | 6 | a0001c0001t0001g0290 a0001c0001t0003g0258 a0001c0001t0003g0291 others(3): Show |
6 | HG02572.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+2120dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2502843 | ||||||
| chr4:2502843 | CA | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(252): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.204+2120delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2502843 | ||||||
| chr4:2502984 | G | A | 2 | a0001c0001t0003g0258 a0001c0001t0003g0291 |
2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.204+2246G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502984 | |||||||
| chr4:2503092 | T | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18951.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.204+2354T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503092 | |||||||
| chr4:2503168 | C | G | 1 | a0001c0001t0002g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.204+2430C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503168 | |||||||
| chr4:2503183 | T | C | 43 | a0001c0001t0002g0004 a0001c0001t0002g0122 a0001c0001t0002g0167 others(40): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.204+2445T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503183 | |||||||
| chr4:2503311 | T | G | 14 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0353 others(11): Show |
14 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.204+2573T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503311 | |||||||
| chr4:2503320 | A | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+2582A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503320 | |||||||
| chr4:2503364 | G | T | 98 | a0001c0001t0003g0171 a0001c0001t0003g0218 a0001c0001t0003g0219 others(95): Show |
99 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.204+2626G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503364 | |||||||
| chr4:2503517 | C | T | 80 | a0001c0001t0003g0171 a0001c0001t0003g0218 a0001c0001t0003g0219 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.204+2779C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503517 | |||||||
| chr4:2503580 | A | G | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+2842A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503580 | |||||||
| chr4:2503658 | C | T | 1 | a0001c0001t0019g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.204+2920C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503658 | |||||||
| chr4:2503736 | C | G | 1 | a0001c0001t0005g0016 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.204+2998C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503736 | |||||||
| chr4:2503800 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.204+3062C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503800 | |||||||
| chr4:2503802 | G | C | 18 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(15): Show |
18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.204+3064G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503802 | |||||||
| chr4:2503824 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+3086C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503824 | |||||||
| chr4:2503879 | C | T | 98 | a0001c0001t0003g0171 a0001c0001t0003g0218 a0001c0001t0003g0219 others(95): Show |
99 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.204+3141C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503879 | |||||||
| chr4:2503996 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.204+3258C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503996 | |||||||
| chr4:2504000 | T | G | 14 | a0001c0001t0008g0066 a0001c0001t0008g0282 a0001c0001t0008g0305 others(11): Show |
14 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.204+3262T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504000 | |||||||
| chr4:2504260 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0285 a0001c0001t0001g0286 others(20): Show |
23 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.204+3522G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504260 | |||||||
| chr4:2504267 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0142 others(2): Show |
5 | HG01106.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+3529G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504267 | |||||||
| chr4:2504276 | G | A | 1 | a0001c0001t0023g0023 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.204+3538G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504276 | |||||||
| chr4:2504392 | C | G | 1 | a0001c0001t0003g0229 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.204+3654C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504392 | |||||||
| chr4:2504441 | T | G | 3 | a0001c0003t0014g0357 a0001c0003t0014g0370 a0001c0003t0021g0306 |
3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+3703T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504441 | |||||||
| chr4:2504482 | T | A | 14 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0353 others(11): Show |
14 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.204+3744T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504482 | |||||||
| chr4:2504523 | C | CATTT | 4 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0288 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+3785_204+3786i others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504523 | |||||||
| chr4:2504524 | T | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0285 others(5): Show |
8 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+3786T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504524 | |||||||
| chr4:2504524 | T | TTTTA | 92 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.204+3826_204+3829d others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | ||||||
| chr4:2504524 | T | TTTTATTT others(1): Show |
44 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0060 others(41): Show |
45 | HG00140.hp1 HG00673.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.204+3822_204+3829d others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | ||||||
| chr4:2504524 | T | TTTTATTT others(5): Show |
3 | a0001c0001t0001g0355 a0001c0001t0006g0162 a0001c0001t0006g0163 |
3 | HG02630.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.204+3818_204+3829d others(14): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | ||||||
| chr4:2504524 | TTTTA | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0056 others(105): Show |
109 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.204+3826_204+3829d others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | ||||||
| chr4:2504524 | TTTTATTT others(5): Show |
T | 17 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0049 others(14): Show |
17 | HG00609.hp1 HG01975.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.204+3818_204+3829d others(14): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | ||||||
| chr4:2504524 | TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0007 | 2 | HG00639.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.204+3814_204+3829d others(18): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | ||||||
| chr4:2504613 | T | C | 17 | a0001c0001t0008g0066 a0001c0001t0008g0282 a0001c0001t0008g0305 others(14): Show |
17 | HG00544.hp2 HG00609.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.204+3875T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504613 | |||||||
| chr4:2504726 | A | AT | 106 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0076 others(103): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.204+4009dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | ||||||
| chr4:2504726 | A | ATT | 10 | a0001c0001t0001g0150 a0001c0001t0002g0172 a0001c0001t0002g0189 others(7): Show |
10 | HG00741.hp2 HG01099.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.204+4008_204+4009d others(4): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | ||||||
| chr4:2504726 | A | ATTT | 6 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0011g0364 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+4007_204+4009d others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | ||||||
| chr4:2504726 | A | ATTTTTTT others(1): Show |
7 | a0001c0001t0008g0066 a0001c0001t0008g0282 a0001c0001t0008g0305 others(4): Show |
7 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+4002_204+4009d others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | ||||||
| chr4:2504726 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0015g0350 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.204+3993_204+4009d others(19): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | ||||||
| chr4:2504726 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0015g0351 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.204+3992_204+4009d others(20): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | ||||||
| chr4:2504726 | AT | A | 7 | a0001c0001t0001g0073 a0001c0001t0001g0100 a0001c0001t0001g0107 others(4): Show |
7 | HG01515.hp1 HG01515.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+4009delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | ||||||
| chr4:2504986 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.204+4248G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504986 | |||||||
| chr4:2505051 | T | A | 7 | a0001c0001t0002g0004 a0001c0001t0002g0167 a0001c0001t0002g0183 others(4): Show |
8 | NA18939.hp1 NA18952.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+4313T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505051 | |||||||
| chr4:2505091 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4353G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505091 | |||||||
| chr4:2505177 | C | G | 6 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(3): Show |
6 | HG01256.hp1 HG01258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+4439C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505177 | |||||||
| chr4:2505233 | G | C | 21 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(18): Show |
21 | HG01074.hp1 HG01081.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.204+4495G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505233 | |||||||
| chr4:2505328 | C | CT | 64 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.204+4605dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505328 | ||||||
| chr4:2505328 | CT | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0286 others(4): Show |
7 | HG02895.hp2 HG02976.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+4605delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505328 | ||||||
| chr4:2505353 | T | G | 1 | a0001c0001t0005g0016 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.204+4615T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505353 | |||||||
| chr4:2505356 | C | T | 17 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(14): Show |
17 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.204+4618C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505356 | |||||||
| chr4:2505364 | T | C | 4 | a0001c0001t0001g0071 a0001c0001t0005g0016 a0001c0003t0014g0357 others(1): Show |
4 | HG01167.hp2 HG02647.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4626T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505364 | |||||||
| chr4:2505365 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.204+4627G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505365 | |||||||
| chr4:2505370 | A | G | 101 | a0001c0001t0001g0035 a0001c0001t0001g0047 a0001c0001t0001g0064 others(98): Show |
102 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.204+4632A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505370 | |||||||
| chr4:2505379 | A | G | 12 | a0001c0001t0004g0356 a0001c0001t0007g0006 a0001c0001t0007g0303 others(9): Show |
13 | HG01891.hp1 HG02280.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.204+4641A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505379 | |||||||
| chr4:2505388 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.204+4650C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505388 | |||||||
| chr4:2505394 | T | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+4656T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505394 | |||||||
| chr4:2505405 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.204+4667C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505405 | |||||||
| chr4:2505418 | T | C | 3 | a0001c0001t0002g0190 a0001c0001t0002g0265 a0001c0001t0003g0267 |
3 | HG00280.hp2 HG00323.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.204+4680T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505418 | |||||||
| chr4:2505425 | A | C | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.204+4687A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505425 | |||||||
| chr4:2505427 | A | G | 16 | a0001c0001t0001g0304 a0001c0001t0003g0273 a0001c0001t0004g0270 others(13): Show |
16 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.204+4689A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505427 | |||||||
| chr4:2505437 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.204+4699T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505437 | |||||||
| chr4:2505444 | G | C | 1 | a0001c0001t0002g0195 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.204+4706G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505444 | |||||||
| chr4:2505450 | A | C | 13 | a0001c0001t0001g0262 a0001c0001t0001g0298 a0001c0001t0001g0299 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.204+4712A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505450 | |||||||
| chr4:2505450 | A | T | 5 | a0001c0001t0001g0353 a0001c0001t0001g0354 a0001c0001t0001g0355 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+4712A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505450 | |||||||
| chr4:2505455 | A | T | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+4717A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505455 | |||||||
| chr4:2505464 | T | G | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+4726T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505464 | |||||||
| chr4:2505470 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0091 others(4): Show |
8 | HG01934.hp2 HG02647.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+4732T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505470 | |||||||
| chr4:2505473 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+4735C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505473 | |||||||
| chr4:2505474 | C | T | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+4736C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505474 | |||||||
| chr4:2505475 | G | A | 2 | a0001c0001t0001g0044 a0001c0003t0021g0306 |
2 | HG01167.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.204+4737G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505475 | |||||||
| chr4:2505477 | C | T | 1 | a0001c0001t0005g0013 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.204+4739C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505477 | |||||||
| chr4:2505482 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.204+4744C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505482 | |||||||
| chr4:2505483 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0004g0356 |
3 | HG02970.hp1 HG03579.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.204+4745A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505483 | |||||||
| chr4:2505486 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.204+4748C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505486 | |||||||
| chr4:2505505 | T | G | 3 | a0001c0001t0002g0211 a0001c0001t0015g0350 a0001c0001t0015g0351 |
3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.204+4767T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505505 | |||||||
| chr4:2505526 | C | T | 1 | a0001c0001t0032g0360 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.204+4788C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505526 | |||||||
| chr4:2505527 | A | G | 147 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0039 others(144): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.204+4789A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505527 | |||||||
| chr4:2505531 | T | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0092 a0001c0001t0001g0094 others(3): Show |
6 | HG00408.hp1 HG00558.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+4793T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505531 | |||||||
| chr4:2505532 | A | T | 4 | a0001c0001t0001g0353 a0001c0001t0001g0354 a0001c0001t0001g0355 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+4794A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505532 | |||||||
| chr4:2505533 | G | C | 51 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0079 others(48): Show |
52 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.204+4795G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505533 | |||||||
| chr4:2505535 | C | T | 2 | a0001c0001t0002g0168 a0001c0001t0009g0256 |
2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.204+4797C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505535 | |||||||
| chr4:2505536 | A | G | 1 | a0001c0001t0003g0267 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.204+4798A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505536 | |||||||
| chr4:2505546 | C | A | 7 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0353 others(4): Show |
7 | HG02145.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+4808C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505546 | |||||||
| chr4:2505546 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.204+4808C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505546 | |||||||
| chr4:2505547 | G | A | 124 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0078 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.204+4809G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505547 | |||||||
| chr4:2505547 | G | C | 1 | a0001c0001t0015g0351 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.204+4809G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505547 | |||||||
| chr4:2505560 | C | T | 224 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0024 others(221): Show |
227 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.204+4822C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505560 | |||||||
| chr4:2505568 | G | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0150 a0001c0001t0001g0285 others(30): Show |
33 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.204+4830G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505568 | |||||||
| chr4:2505572 | G | A | 312 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.204+4834G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505572 | |||||||
| chr4:2505575 | T | C | 1 | a0001c0001t0012g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.204+4837T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505575 | |||||||
| chr4:2505576 | C | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.204+4838C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505576 | |||||||
| chr4:2505584 | C | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(260): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.204+4846C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505584 | |||||||
| chr4:2505600 | T | C | 80 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(77): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.204+4862T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505600 | |||||||
| chr4:2505604 | T | C | 66 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(63): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.204+4866T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505604 | |||||||
| chr4:2505614 | C | G | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.204+4876C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505614 | |||||||
| chr4:2505614 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(234): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.204+4876C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505614 | |||||||
| chr4:2505616 | C | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+4878C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505616 | |||||||
| chr4:2505617 | G | A | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+4879G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505617 | |||||||
| chr4:2505618 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+4880C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505618 | |||||||
| chr4:2505620 | C | T | 1 | a0001c0001t0012g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.204+4882C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505620 | |||||||
| chr4:2505621 | G | A | 2 | a0001c0001t0011g0364 a0001c0001t0011g0367 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.204+4883G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505621 | |||||||
| chr4:2505629 | G | A | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.204+4891G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505629 | |||||||
| chr4:2505717 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0285 a0001c0001t0001g0286 others(19): Show |
22 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.204+4979G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505717 | |||||||
| chr4:2505723 | C | CTT | 6 | a0001c0001t0001g0309 a0001c0001t0008g0305 a0001c0001t0008g0321 others(3): Show |
6 | HG01258.hp1 HG02071.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+5014_204+5015d others(4): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | ||||||
| chr4:2505723 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0015g0350 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.204+4991_204+5015d others(27): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | ||||||
| chr4:2505723 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0015g0351 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.204+4990_204+5015d others(28): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | ||||||
| chr4:2505723 | CT | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.204+5015delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | ||||||
| chr4:2505723 | CTT | C | 87 | a0001c0001t0001g0008 a0001c0001t0001g0065 a0001c0001t0001g0083 others(84): Show |
87 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.204+5014_204+5015d others(4): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | ||||||
| chr4:2505723 | CTTT | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0262 a0001c0001t0001g0298 others(12): Show |
16 | HG01109.hp2 HG01243.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.204+5013_204+5015d others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | ||||||
| chr4:2505723 | CTTTT | C | 43 | a0001c0001t0002g0004 a0001c0001t0002g0122 a0001c0001t0002g0167 others(40): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.204+5012_204+5015d others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | ||||||
| chr4:2505723 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0008g0066 a0001c0001t0008g0327 |
2 | HG00609.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.204+5005_204+5015d others(13): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | ||||||
| chr4:2505741 | T | C | 2 | a0002c0004t0001g0055 a0002c0004t0001g0057 |
2 | HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.204+5003T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505741 | |||||||
| chr4:2505759 | G | T | 1 | a0001c0001t0032g0360 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.204+5021G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505759 | |||||||
| chr4:2505790 | G | A | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+5052G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505790 | |||||||
| chr4:2505907 | G | A | 1 | a0001c0001t0004g0352 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.204+5169G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505907 | |||||||
| chr4:2505910 | C | T | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+5172C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505910 | |||||||
| chr4:2506081 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0115 |
2 | HG01175.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.204+5343A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506081 | |||||||
| chr4:2506180 | T | C | 39 | a0001c0001t0001g0008 a0001c0001t0001g0285 a0001c0001t0001g0286 others(36): Show |
39 | HG01167.hp2 HG01243.hp2 HG02145.hp1 others(36): Show |
intron_variant | MODIFIER | c.204+5442T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506180 | |||||||
| chr4:2506189 | CT | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.204+5456delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2506189 | ||||||
| chr4:2506200 | CT | C | 6 | a0001c0001t0003g0171 a0001c0001t0003g0243 a0001c0001t0003g0248 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+5463delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506200 | |||||||
| chr4:2506215 | G | A | 52 | a0001c0001t0002g0004 a0001c0001t0002g0122 a0001c0001t0002g0167 others(49): Show |
53 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.204+5477G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506215 | |||||||
| chr4:2506219 | T | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0058 others(1): Show |
4 | HG00642.hp2 HG00735.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+5481T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506219 | |||||||
| chr4:2506223 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.204+5485G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506223 | |||||||
| chr4:2506313 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0104 |
2 | NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.204+5575A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506313 | |||||||
| chr4:2506356 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.205-5600G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506356 | |||||||
| chr4:2506382 | A | G | 12 | a0001c0001t0008g0066 a0001c0001t0008g0282 a0001c0001t0008g0305 others(9): Show |
12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-5574A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506382 | |||||||
| chr4:2506462 | G | A | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-5494G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506462 | |||||||
| chr4:2506478 | G | A | 2 | a0001c0001t0003g0258 a0001c0001t0003g0291 |
2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.205-5478G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506478 | |||||||
| chr4:2506571 | C | CT | 12 | a0001c0001t0008g0066 a0001c0001t0008g0282 a0001c0001t0008g0305 others(9): Show |
12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-5376dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2506571 | ||||||
| chr4:2506574 | T | C | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-5382T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506574 | |||||||
| chr4:2506635 | A | C | 1 | a0001c0001t0006g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.205-5321A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506635 | |||||||
| chr4:2506636 | C | T | 1 | a0001c0001t0006g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.205-5320C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506636 | |||||||
| chr4:2506727 | C | G | 22 | a0001c0001t0003g0258 a0001c0001t0003g0271 a0001c0001t0003g0272 others(19): Show |
22 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.205-5229C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506727 | |||||||
| chr4:2506781 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.205-5175G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506781 | |||||||
| chr4:2507381 | A | G | 1 | a0001c0001t0001g0371 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.205-4575A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507381 | |||||||
| chr4:2507505 | C | T | 1 | a0001c0001t0022g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.205-4451C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507505 | |||||||
| chr4:2507602 | C | A | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-4354C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507602 | |||||||
| chr4:2507678 | G | A | 2 | a0001c0001t0005g0296 a0001c0001t0005g0297 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.205-4278G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507678 | |||||||
| chr4:2507759 | C | T | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.205-4197C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507759 | |||||||
| chr4:2508104 | C | T | 6 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(3): Show |
6 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-3852C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508104 | |||||||
| chr4:2508147 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.205-3809G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508147 | |||||||
| chr4:2508186 | A | C | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.205-3770A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508186 | |||||||
| chr4:2508248 | T | G | 1 | a0001c0001t0002g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.205-3708T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508248 | |||||||
| chr4:2508357 | T | C | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.205-3599T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508357 | |||||||
| chr4:2508361 | C | T | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-3595C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508361 | |||||||
| chr4:2508400 | C | G | 1 | a0001c0001t0001g0339 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.205-3556C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508400 | |||||||
| chr4:2508592 | T | G | 1 | a0001c0001t0002g0194 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.205-3364T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508592 | |||||||
| chr4:2508662 | G | A | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.205-3294G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508662 | |||||||
| chr4:2508754 | A | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(242): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.205-3202A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508754 | |||||||
| chr4:2508758 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.205-3198G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508758 | |||||||
| chr4:2508911 | C | CT | 98 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0150 others(95): Show |
98 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.205-3020dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2508911 | ||||||
| chr4:2508911 | C | CTT | 37 | a0001c0001t0001g0108 a0001c0001t0001g0149 a0001c0001t0001g0316 others(34): Show |
38 | HG01074.hp1 HG01081.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.205-3021_205-3020d others(4): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2508911 | ||||||
| chr4:2508911 | C | CTTT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.205-3022_205-3020d others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2508911 | ||||||
| chr4:2508911 | C | CTTTT | 19 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(16): Show |
19 | HG00099.hp2 HG01099.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-3023_205-3020d others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2508911 | ||||||
| chr4:2509007 | C | T | 1 | a0001c0001t0009g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.205-2949C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509007 | |||||||
| chr4:2509009 | C | G | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.205-2947C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509009 | |||||||
| chr4:2509012 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.205-2944G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509012 | |||||||
| chr4:2509036 | A | C | 2 | a0001c0001t0015g0350 a0001c0001t0015g0351 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-2920A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509036 | |||||||
| chr4:2509072 | C | G | 1 | a0001c0001t0003g0268 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.205-2884C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509072 | |||||||
| chr4:2509162 | G | A | 12 | a0001c0001t0008g0066 a0001c0001t0008g0282 a0001c0001t0008g0305 others(9): Show |
12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-2794G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509162 | |||||||
| chr4:2509228 | T | C | 2 | a0001c0001t0002g0177 a0001c0001t0002g0186 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.205-2728T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509228 | |||||||
| chr4:2509308 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.205-2648C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509308 | |||||||
| chr4:2509344 | A | T | 1 | a0001c0001t0003g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.205-2612A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509344 | |||||||
| chr4:2509451 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.205-2505C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509451 | |||||||
| chr4:2509469 | C | T | 1 | a0001c0001t0007g0329 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.205-2487C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509469 | |||||||
| chr4:2509508 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.205-2448G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509508 | |||||||
| chr4:2509525 | T | G | 18 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(15): Show |
18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.205-2431T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509525 | |||||||
| chr4:2509650 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.205-2306G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509650 | |||||||
| chr4:2509768 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.205-2188G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509768 | |||||||
| chr4:2509890 | C | T | 1 | a0001c0001t0004g0280 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.205-2066C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509890 | |||||||
| chr4:2509976 | A | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.205-1980A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509976 | |||||||
| chr4:2510089 | G | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.205-1867G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510089 | |||||||
| chr4:2510289 | G | C | 123 | a0001c0001t0001g0262 a0001c0001t0003g0170 a0001c0001t0003g0171 others(120): Show |
124 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.205-1667G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510289 | |||||||
| chr4:2510324 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0029g0363 |
2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.205-1632C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510324 | |||||||
| chr4:2510327 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(121): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.205-1629A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510327 | |||||||
| chr4:2510480 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03490.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.205-1476C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510480 | |||||||
| chr4:2510514 | C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.205-1442C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510514 | |||||||
| chr4:2510517 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.205-1439C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510517 | |||||||
| chr4:2510736 | C | A | 12 | a0001c0001t0007g0006 a0001c0001t0007g0303 a0001c0001t0007g0308 others(9): Show |
13 | HG01891.hp1 HG02280.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.205-1220C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510736 | |||||||
| chr4:2510791 | C | G | 1 | a0001c0001t0005g0012 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.205-1165C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510791 | |||||||
| chr4:2511216 | T | TAAGGTCC others(54): Show |
1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.205-330_205-270dup others(61): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | ||||||
| chr4:2511216 | TAAGGTCC others(54): Show |
T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(151): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.205-330_205-270del others(61): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | ||||||
| chr4:2511216 | TAAGGTCC others(115): Show |
T | 19 | a0001c0001t0001g0101 a0001c0001t0001g0164 a0001c0001t0001g0298 others(16): Show |
19 | HG00544.hp2 HG00609.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-391_205-270del | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | ||||||
| chr4:2511216 | TAAGGTCC others(176): Show |
T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0052 others(105): Show |
110 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.205-452_205-270del | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | ||||||
| chr4:2511216 | TAAGGTCC others(237): Show |
T | 3 | a0001c0001t0001g0262 a0001c0003t0014g0357 a0001c0003t0014g0370 |
3 | HG01243.hp2 HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.205-513_205-270del | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | ||||||
| chr4:2511216 | TAAGGTCC others(359): Show |
T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.205-635_205-270del | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | ||||||
| chr4:2511347 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.205-609C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511347 | |||||||
| chr4:2511446 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.205-510C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511446 | |||||||
| chr4:2511467 | C | T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0107 others(4): Show |
7 | HG00140.hp2 HG01069.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-489C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511467 | |||||||
| chr4:2511532 | G | C | 2 | a0001c0001t0003g0258 a0001c0001t0003g0291 |
2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.205-424G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511532 | |||||||
| chr4:2511574 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.205-382A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511574 | |||||||
| chr4:2511888 | G | C | 117 | a0001c0001t0003g0170 a0001c0001t0003g0171 a0001c0001t0003g0218 others(114): Show |
118 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.205-68G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511888 | |||||||
| chr4:2511893 | G | A | 338 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(335): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.205-63G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511893 | |||||||
| chr4:2511897 | A | G | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0024 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.205-59A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511897 | |||||||
| chr4:2512027 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.214+62G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512027 | |||||||
| chr4:2512086 | A | T | 1 | a0001c0001t0003g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.214+121A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512086 | |||||||
| chr4:2512094 | G | A | 2 | a0001c0003t0014g0357 a0001c0003t0014g0370 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.214+129G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512094 | |||||||
| chr4:2512115 | A | G | 336 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(333): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.214+150A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512115 | |||||||
| chr4:2512241 | G | A | 11 | a0001c0001t0003g0171 a0001c0001t0003g0224 a0001c0001t0003g0242 others(8): Show |
11 | HG01255.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.215-197G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512241 | |||||||
| chr4:2512606 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.374+9G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 6/7 | chr4 | 2512606 | |||||||
| chr4:2512651 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0285 a0001c0001t0001g0286 others(19): Show |
22 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.374+54C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 6/7 | chr4 | 2512651 | |||||||
| chr4:2512960 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.375-123G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 6/7 | chr4 | 2512960 | |||||||
| chr4:2513335 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.423+204A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/7 | chr4 | 2513335 | |||||||
| chr4:2513341 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.423+210C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/7 | chr4 | 2513341 | |||||||
| chr4:2513424 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0127 a0001c0001t0025g0126 |
3 | NA18967.hp2 NA19007.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.424-246A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/7 | chr4 | 2513424 | |||||||
| chr4:2513550 | G | C | 18 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(15): Show |
18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.424-120G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/7 | chr4 | 2513550 |