Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 441054 |
| ensemblid | ENSG00000205129.9 |
| hgncid | 34346 |
| symbol | C4orf47 |
| name | cilia and flagella associated protein 96 |
| refseq_nuc | NM_001114357.3 |
| refseq_prot | NP_001107829.1 |
| ensembl_nuc | ENST00000378850.5 |
| ensembl_prot | ENSP00000368127.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 185426254 |
| end | 185449826 |
| strand | + |
| ver | v1.2 |
| region | chr4:185426254-185449826 |
| region5000 | chr4:185421254-185454826 |
| regionname0 | C4orf47_chr4_185426254_185449826 |
| regionname5000 | C4orf47_chr4_185421254_185454826 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 309 | 321 | 79 | 56 | 137 | 14 | 34 | 99 | C4orf47_chr4_185421254_185454826 | C4orf47 | MPAEG others(304): Show |
chr4 | 185421254 | 185454826 |
| a0002 | 0/1 | 309 | 25 | 5 | 10 | 1 | 0 | 8 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | MPAEG others(304): Show |
chr4 | 185421254 | 185454826 |
| a0003 | 0/0 | 309 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | MPAEG others(304): Show |
chr4 | 185421254 | 185454826 |
| a0004 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | MPAEG others(304): Show |
chr4 | 185421254 | 185454826 |
| a0005 | 0/0 | 309 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | MPAEG others(304): Show |
chr4 | 185421254 | 185454826 |
| a0006 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | MPAEG others(304): Show |
chr4 | 185421254 | 185454826 |
| a0007 | 0/0 | 309 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | MPAEG others(304): Show |
chr4 | 185421254 | 185454826 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 927 | 313 | 73 | 55 | 136 | 14 | 34 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0001c0004 | 0/0 | 927 | 5 | 4 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0001c0007 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0001c0009 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0001c0010 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0002c0002 | 0/1 | 927 | 25 | 5 | 10 | 1 | 0 | 8 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0003c0003 | 0/0 | 927 | 8 | 8 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0004c0011 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0005c0006 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0006c0005 | 0/0 | 927 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 | ||
| a0007c0008 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | ATGCC others(922): Show |
chr4 | 185421254 | 185454826 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1333 | 218 | 33 | 36 | 116 | 9 | 24 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0001t0002 | 0/0 | 1333 | 36 | 20 | 1 | 8 | 1 | 6 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0001t0003 | 0/0 | 1333 | 36 | 3 | 14 | 12 | 4 | 3 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0001t0004 | 0/0 | 1333 | 17 | 13 | 3 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0001t0005 | 1/0 | 1333 | 3 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0001t0006 | 0/0 | 1333 | 3 | 2 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | GGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0004t0001 | 0/0 | 1333 | 3 | 2 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0004t0007 | 0/0 | 1333 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0007t0002 | 0/0 | 1333 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0009t0003 | 0/0 | 1333 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0001c0010t0001 | 0/0 | 1333 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0002c0002t0001 | 0/1 | 1333 | 25 | 5 | 10 | 1 | 0 | 8 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0003c0003t0001 | 0/0 | 1333 | 5 | 5 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0003c0003t0002 | 0/0 | 1333 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0004c0011t0001 | 0/0 | 1333 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0005c0006t0003 | 0/0 | 1333 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0006c0005t0001 | 0/0 | 1333 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| a0007c0008t0001 | 0/0 | 1333 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | AGAGG others(1328): Show |
chr4 | 185421254 | 185454826 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0002 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0007 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0005g0008 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0004t0007g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0007t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0009t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0001c0010t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0003c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0003c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0003c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0003c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0003c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0003c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0003c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0004c0011t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0005c0006t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0006c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| a0007c0008t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0033 | EUR | GBR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0120 | EUR | FIN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0194 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0248 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0099 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0055 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0013 | EUR | IBS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0183 | EUR | IBS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | IBS | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01884 | hp1 | a0001 | c0004 | t0007 | g0039 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02129 | hp2 | a0005 | c0006 | t0003 | g0002 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | CDX | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | CDX | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0051 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02280 | hp1 | a0006 | c0005 | t0001 | g0079 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02615 | hp2 | a0001 | c0010 | t0001 | g0053 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0060 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02809 | hp2 | a0001 | c0007 | t0002 | g0217 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02896 | hp1 | a0003 | c0003 | t0002 | g0084 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02976 | hp1 | a0003 | c0003 | t0002 | g0068 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0111 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0125 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0090 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0086 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0269 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0093 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0025 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0113 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0205 | SAS | BEB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | STU | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0230 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | CHB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0056 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18975 | hp1 | a0001 | c0009 | t0003 | g0002 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18981 | hp1 | a0007 | c0008 | t0001 | g0137 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA19240 | hp2 | a0001 | c0004 | t0007 | g0039 | AFR | YRI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | ASW | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ASW | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | TSI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | GIH | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02109 | hp2 | a0004 | c0011 | t0001 | g0258 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02559 | hp1 | a0003 | c0003 | t0002 | g0057 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0195 | AFR | MSL | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | USA | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | LWK | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0094 | REF | REF | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0008 | REF | REF | C4orf47_chr4_185421254_185454826 | C4orf47 | chr4 | 185421254 | 185454826 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185432078 | T | C | 1 | a0006 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.197T>C | p.Phe66Ser | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/8 | 418/1333 | 197/930 | 66/309 | chr4 | 185432078 | |||
| chr4:185432131 | C | T | 1 | a0004 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.250C>T | p.Arg84Trp | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/8 | 471/1333 | 250/930 | 84/309 | chr4 | 185432131 | |||
| chr4:185436101 | G | A | 1 | a0003 | 8 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
missense_variant | MODERATE | c.376G>A | p.Ala126Thr | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 4/8 | 597/1333 | 376/930 | 126/309 | chr4 | 185436101 | |||
| chr4:185440597 | C | T | 1 | a0007 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.592C>T | p.His198Tyr | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/8 | 813/1333 | 592/930 | 198/309 | chr4 | 185440597 | |||
| chr4:185445027 | G | A | 1 | a0002 | 24 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(21): Show |
missense_variant | MODERATE | c.778G>A | p.Ala260Thr | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/8 | 999/1333 | 778/930 | 260/309 | chr4 | 185445027 | |||
| chr4:185445118 | T | C | 1 | a0005 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.869T>C | p.Leu290Ser | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/8 | 1090/1333 | 869/930 | 290/309 | chr4 | 185445118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185436178 | A | G | 1 | a0001c0010 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.453A>G | p.Gly151Gly | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 4/8 | 674/1333 | 453/930 | 151/309 | chr4 | 185436178 | |||
| chr4:185436350 | A | G | 1 | a0001c0009 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.525A>G | p.Leu175Leu | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/8 | 746/1333 | 525/930 | 175/309 | chr4 | 185436350 | |||
| chr4:185440617 | C | T | 1 | a0001c0007 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.612C>T | p.Asp204Asp | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/8 | 833/1333 | 612/930 | 204/309 | chr4 | 185440617 | |||
| chr4:185440701 | G | A | 1 | a0001c0004 | 5 | HG00733.hp2 HG01884.hp1 HG03471.hp2 others(2): Show |
synonymous_variant | LOW | c.696G>A | p.Pro232Pro | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/8 | 917/1333 | 696/930 | 232/309 | chr4 | 185440701 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185426254 | A | G | 1 | a0001c0001t0006 | 3 | HG01099.hp1 HG03516.hp1 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-221A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/8 | 3158 | chr4 | 185426254 | ||||||
| chr4:185426289 | G | A | 1 | a0001c0004t0007 | 2 | HG01884.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-186G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/8 | 3123 | chr4 | 185426289 | ||||||
| chr4:185429405 | C | T | 4 | a0001c0001t0003 a0001c0001t0004 a0001c0009t0003 others(1): Show |
55 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/8 | chr4 | 185429405 | |||||||
| chr4:185449692 | C | T | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0007t0002 others(1): Show |
57 | HG00642.hp1 HG01109.hp2 HG01934.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*48C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 8/8 | 48 | chr4 | 185449692 | ||||||
| chr4:185449802 | G | C | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(14): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*158G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 8/8 | 158 | chr4 | 185449802 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:185426481 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-79+85T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426481 | |||||||
| chr4:185426539 | T | A | 1 | a0001c0001t0002g0021 | 2 | NA18964.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-79+143T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426539 | |||||||
| chr4:185426811 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-79+415C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426811 | |||||||
| chr4:185426879 | CAAA | C | 16 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0054 others(13): Show |
18 | HG01243.hp1 HG01433.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-79+517_-79+519del others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426879 | CAAAA | C | 21 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0070 others(18): Show |
24 | HG00741.hp1 HG01081.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.-79+516_-79+519del others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426879 | CAAAAA | C | 17 | a0001c0001t0001g0029 a0001c0001t0001g0095 a0001c0001t0001g0096 others(14): Show |
22 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-79+515_-79+519del others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426879 | CAAAAAAA others(3): Show |
C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0101 others(10): Show |
16 | HG00597.hp2 HG00642.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.-79+510_-79+519del others(10): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426879 | CAAAAAAA others(4): Show |
C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(102): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-79+509_-79+519del others(11): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426879 | CAAAAAAA others(5): Show |
C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0019 others(76): Show |
102 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-79+508_-79+519del others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426879 | CAAAAAAA others(6): Show |
C | 9 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(6): Show |
9 | HG02083.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-79+507_-79+519del others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426879 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0268 a0001c0001t0002g0020 a0001c0001t0002g0267 |
5 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+506_-79+519del others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426879 | CAAAAAAA others(10): Show |
C | 1 | a0002c0002t0001g0269 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-79+503_-79+519del others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426879 | CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0003g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-79+500_-79+519del others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185426879 | ||||||
| chr4:185426918 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-79+522G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426918 | |||||||
| chr4:185426962 | G | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0046 a0001c0001t0002g0047 |
4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-79+566G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185426962 | |||||||
| chr4:185427048 | G | C | 1 | a0001c0004t0001g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-79+652G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427048 | |||||||
| chr4:185427064 | C | CA | 17 | a0001c0001t0001g0112 a0001c0001t0002g0088 a0001c0001t0002g0100 others(14): Show |
18 | HG00639.hp1 HG00733.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.-79+683dupA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185427064 | ||||||
| chr4:185427064 | CA | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-79+683delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185427064 | ||||||
| chr4:185427289 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-79+893G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427289 | |||||||
| chr4:185427356 | A | G | 1 | a0002c0002t0001g0069 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-79+960A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427356 | |||||||
| chr4:185427433 | T | C | 13 | a0001c0001t0001g0124 a0001c0001t0001g0229 a0001c0001t0003g0199 others(10): Show |
20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-79+1037T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427433 | |||||||
| chr4:185427481 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-79+1085C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427481 | |||||||
| chr4:185427663 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-79+1267G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427663 | |||||||
| chr4:185427668 | GAGAATTC others(319): Show |
G | 14 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0002t0001g0028 others(11): Show |
18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-79+1278_-78-1335d others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185427668 | ||||||
| chr4:185427970 | C | T | 13 | a0001c0001t0001g0124 a0001c0001t0001g0229 a0001c0001t0003g0199 others(10): Show |
20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-78-1364C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185427970 | |||||||
| chr4:185428029 | T | A | 2 | a0001c0001t0006g0125 a0001c0001t0006g0230 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-78-1305T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428029 | |||||||
| chr4:185428086 | CA | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-78-1232delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428086 | ||||||
| chr4:185428086 | CAA | C | 47 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(44): Show |
64 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.-78-1233_-78-1232d others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428086 | ||||||
| chr4:185428109 | T | G | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78-1225T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428109 | |||||||
| chr4:185428111 | A | T | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78-1223A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428111 | |||||||
| chr4:185428162 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-78-1172A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428162 | |||||||
| chr4:185428165 | T | A | 2 | a0001c0001t0003g0033 a0001c0001t0003g0130 |
3 | HG00140.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-78-1169T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428165 | |||||||
| chr4:185428295 | C | A | 4 | a0001c0001t0002g0022 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
5 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78-1039C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428295 | |||||||
| chr4:185428398 | A | G | 13 | a0001c0001t0001g0124 a0001c0001t0001g0229 a0001c0001t0003g0199 others(10): Show |
20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-78-936A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428398 | |||||||
| chr4:185428446 | G | A | 1 | a0001c0001t0001g0041 | 2 | NA18998.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-78-888G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428446 | |||||||
| chr4:185428556 | TA | T | 70 | a0001c0001t0001g0019 a0001c0001t0001g0098 a0001c0001t0001g0124 others(67): Show |
91 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.-78-764delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428556 | ||||||
| chr4:185428556 | TAA | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(160): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-78-765_-78-764del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428556 | ||||||
| chr4:185428561 | A | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(31): Show |
43 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.-78-773A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428561 | |||||||
| chr4:185428582 | AC | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0115 others(14): Show |
25 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.-78-751delC | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428582 | |||||||
| chr4:185428583 | C | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | NA19064.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-78-751C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428583 | |||||||
| chr4:185428583 | CA | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-78-741delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185428583 | ||||||
| chr4:185428587 | A | C | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0265 |
3 | HG02647.hp2 NA18948.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-78-747A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428587 | |||||||
| chr4:185428611 | C | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-78-723C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428611 | |||||||
| chr4:185428802 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0229 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-78-532T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428802 | |||||||
| chr4:185428878 | T | G | 20 | a0001c0001t0001g0098 a0001c0010t0001g0053 a0002c0002t0001g0009 others(17): Show |
24 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-78-456T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428878 | |||||||
| chr4:185428909 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(158): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-78-425C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185428909 | |||||||
| chr4:185429033 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-78-301G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429033 | |||||||
| chr4:185429044 | A | C | 1 | a0001c0001t0003g0191 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-78-290A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429044 | |||||||
| chr4:185429075 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-78-259G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429075 | |||||||
| chr4:185429081 | G | A | 33 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(30): Show |
42 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.-78-253G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429081 | |||||||
| chr4:185429086 | G | C | 1 | a0001c0001t0001g0213 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-78-248G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429086 | |||||||
| chr4:185429181 | C | A | 17 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0002t0001g0028 others(14): Show |
21 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-78-153C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | chr4 | 185429181 | |||||||
| chr4:185429286 | C | CT | 46 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0224 others(43): Show |
62 | HG00544.hp1 HG00642.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.-78-42dupT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 185429286 | ||||||
| chr4:185429705 | G | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0045 others(17): Show |
24 | HG00438.hp1 HG00597.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+194G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429705 | |||||||
| chr4:185429744 | A | G | 1 | a0002c0002t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.100+233A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429744 | |||||||
| chr4:185429760 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.100+249C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429760 | |||||||
| chr4:185429814 | T | A | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100+303T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429814 | |||||||
| chr4:185429850 | TA | T | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+340delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429850 | |||||||
| chr4:185429853 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.100+342G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429853 | |||||||
| chr4:185429853 | G | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0267 |
4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+342G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429853 | |||||||
| chr4:185429854 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0041 others(18): Show |
30 | HG00408.hp1 HG00544.hp2 HG02523.hp2 others(27): Show |
intron_variant | MODIFIER | c.100+343G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429854 | |||||||
| chr4:185429854 | G | C | 13 | a0001c0001t0001g0124 a0001c0001t0001g0229 a0001c0001t0003g0199 others(10): Show |
20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.100+343G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429854 | |||||||
| chr4:185429855 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.100+344C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429855 | |||||||
| chr4:185429855 | C | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0019 others(84): Show |
117 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.100+344C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429855 | |||||||
| chr4:185429919 | A | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.100+408A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429919 | |||||||
| chr4:185429919 | A | G | 43 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0224 others(40): Show |
57 | HG00544.hp1 HG00642.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.100+408A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429919 | |||||||
| chr4:185429926 | G | T | 9 | a0001c0001t0003g0038 a0001c0001t0003g0122 a0001c0001t0003g0129 others(6): Show |
10 | HG01123.hp2 HG01255.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+415G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185429926 | |||||||
| chr4:185430139 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100+628G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430139 | |||||||
| chr4:185430243 | A | G | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+732A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430243 | |||||||
| chr4:185430293 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.100+782C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430293 | |||||||
| chr4:185430458 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.100+947C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430458 | |||||||
| chr4:185430738 | A | G | 4 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
4 | HG02027.hp2 HG02602.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+1227A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430738 | |||||||
| chr4:185430949 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0112 others(12): Show |
18 | HG02698.hp1 HG02738.hp1 HG04184.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-1033C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430949 | |||||||
| chr4:185430982 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.101-1000T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430982 | |||||||
| chr4:185430983 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.101-999G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185430983 | |||||||
| chr4:185431039 | G | A | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.101-943G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431039 | |||||||
| chr4:185431124 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.101-858C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431124 | |||||||
| chr4:185431125 | G | A | 11 | a0001c0001t0003g0199 a0001c0001t0004g0005 a0001c0001t0004g0015 others(8): Show |
18 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-857G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431125 | |||||||
| chr4:185431165 | G | A | 1 | a0001c0004t0001g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101-817G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431165 | |||||||
| chr4:185431209 | CA | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.101-752delA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 185431209 | ||||||
| chr4:185431209 | CAA | C | 22 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0255 others(19): Show |
27 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-753_101-752del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 185431209 | ||||||
| chr4:185431322 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.101-660A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 2/7 | chr4 | 185431322 | |||||||
| chr4:185432202 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp2 | splice_donor_variant&intron_variant | HIGH | c.320+1G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432202 | |||||||
| chr4:185432261 | A | G | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.320+60A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432261 | |||||||
| chr4:185432516 | G | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.320+315G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432516 | |||||||
| chr4:185432614 | G | A | 6 | a0001c0001t0001g0102 a0001c0001t0001g0131 a0001c0001t0001g0134 others(3): Show |
6 | NA18966.hp2 NA18979.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.320+413G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432614 | |||||||
| chr4:185432628 | C | T | 1 | a0002c0002t0001g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.320+427C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432628 | |||||||
| chr4:185432712 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.320+511A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432712 | |||||||
| chr4:185432712 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.320+511A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432712 | |||||||
| chr4:185432810 | C | G | 4 | a0001c0004t0001g0111 a0001c0004t0001g0194 a0001c0004t0001g0195 others(1): Show |
5 | HG00733.hp2 HG01884.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+609C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432810 | |||||||
| chr4:185432861 | T | TA | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.320+672dupA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185432861 | ||||||
| chr4:185432861 | T | TAA | 19 | a0001c0001t0001g0146 a0002c0002t0001g0009 a0002c0002t0001g0025 others(16): Show |
23 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.320+671_320+672dup others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185432861 | ||||||
| chr4:185432932 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.320+731T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432932 | |||||||
| chr4:185432967 | T | G | 1 | a0001c0001t0002g0100 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.320+766T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185432967 | |||||||
| chr4:185433203 | G | A | 2 | a0002c0002t0001g0087 a0002c0002t0001g0099 |
2 | HG00639.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.320+1002G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433203 | |||||||
| chr4:185433248 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.320+1047A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433248 | |||||||
| chr4:185433254 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.320+1053G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433254 | |||||||
| chr4:185433265 | T | C | 1 | a0001c0001t0002g0219 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.320+1064T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433265 | |||||||
| chr4:185433307 | A | G | 1 | a0003c0003t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.320+1106A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433307 | |||||||
| chr4:185433408 | AAAAAAGA others(4): Show |
A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0141 a0001c0001t0001g0179 others(4): Show |
7 | HG01167.hp2 HG02273.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.320+1212_320+1222d others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433408 | ||||||
| chr4:185433409 | AAAAAG | A | 14 | a0001c0001t0001g0070 a0001c0001t0001g0124 a0001c0001t0001g0229 others(11): Show |
20 | HG01167.hp1 HG01975.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.320+1219_320+1223d others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433409 | ||||||
| chr4:185433409 | AAAAAGAA others(3): Show |
A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.320+1214_320+1223d others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433409 | ||||||
| chr4:185433410 | AAAAG | A | 52 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(49): Show |
65 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.320+1213_320+1216d others(6): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433410 | ||||||
| chr4:185433414 | G | A | 5 | a0001c0004t0001g0111 a0001c0004t0001g0194 a0001c0004t0001g0195 others(2): Show |
6 | HG00733.hp2 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.320+1213G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433414 | |||||||
| chr4:185433532 | A | T | 65 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0224 others(62): Show |
85 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.320+1331A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433532 | |||||||
| chr4:185433535 | C | A | 65 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0224 others(62): Show |
85 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.320+1334C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433535 | |||||||
| chr4:185433538 | C | CTAGTA | 65 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0224 others(62): Show |
85 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.320+1338_320+1339i others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433538 | ||||||
| chr4:185433540 | T | A | 65 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0224 others(62): Show |
85 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.320+1339T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433540 | |||||||
| chr4:185433541 | T | A | 65 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0224 others(62): Show |
85 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.320+1340T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433541 | |||||||
| chr4:185433542 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.320+1341G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433542 | |||||||
| chr4:185433603 | T | TAAGAGTG others(348): Show |
1 | a0001c0001t0002g0220 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.320+1417_320+1418i others(357): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185433603 | ||||||
| chr4:185433646 | A | C | 1 | a0002c0002t0001g0055 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.320+1445A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433646 | |||||||
| chr4:185433722 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.320+1521C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433722 | |||||||
| chr4:185433763 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.320+1562G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433763 | |||||||
| chr4:185433784 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.320+1583C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433784 | |||||||
| chr4:185433833 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.320+1632C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433833 | |||||||
| chr4:185433938 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.320+1737G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185433938 | |||||||
| chr4:185434018 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.320+1817T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434018 | |||||||
| chr4:185434128 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.321-1918A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434128 | |||||||
| chr4:185434153 | A | T | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.321-1893A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434153 | |||||||
| chr4:185434381 | A | AT | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.321-1658dupT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185434381 | ||||||
| chr4:185434413 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0046 |
3 | HG02486.hp2 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.321-1633A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434413 | |||||||
| chr4:185434462 | C | T | 5 | a0003c0003t0001g0030 a0003c0003t0001g0056 a0003c0003t0002g0057 others(2): Show |
6 | HG02559.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.321-1584C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434462 | |||||||
| chr4:185434486 | G | C | 1 | a0001c0004t0007g0039 | 2 | HG01884.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.321-1560G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434486 | |||||||
| chr4:185434626 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.321-1420A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434626 | |||||||
| chr4:185434641 | C | T | 1 | a0001c0001t0003g0176 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.321-1405C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434641 | |||||||
| chr4:185434688 | C | CT | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.321-1357dupT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185434688 | ||||||
| chr4:185434692 | A | AC | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.321-1354_321-1353i others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434692 | |||||||
| chr4:185434793 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.321-1253C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434793 | |||||||
| chr4:185434800 | G | A | 1 | a0002c0002t0001g0089 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.321-1246G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434800 | |||||||
| chr4:185434937 | C | A | 1 | a0001c0001t0004g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.321-1109C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434937 | |||||||
| chr4:185434939 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.321-1107C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434939 | |||||||
| chr4:185434966 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.321-1080C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185434966 | |||||||
| chr4:185435273 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0204 |
2 | HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.321-773G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435273 | |||||||
| chr4:185435290 | A | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0267 |
4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.321-756A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435290 | |||||||
| chr4:185435355 | G | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.321-691G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435355 | |||||||
| chr4:185435418 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0095 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.321-628G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435418 | |||||||
| chr4:185435440 | A | G | 14 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0002t0001g0028 others(11): Show |
18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.321-606A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435440 | |||||||
| chr4:185435569 | T | G | 1 | a0001c0004t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.321-477T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435569 | |||||||
| chr4:185435880 | ATATCT | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.321-162_321-158del others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 185435880 | ||||||
| chr4:185435992 | A | C | 1 | a0001c0001t0002g0219 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.321-54A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 3/7 | chr4 | 185435992 | |||||||
| chr4:185436369 | C | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.534+10C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436369 | |||||||
| chr4:185436494 | G | A | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.534+135G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436494 | |||||||
| chr4:185436552 | T | G | 14 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0002t0001g0028 others(11): Show |
18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+193T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436552 | |||||||
| chr4:185436579 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.534+220G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436579 | |||||||
| chr4:185436664 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.534+305C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436664 | |||||||
| chr4:185436665 | G | A | 1 | a0001c0001t0003g0103 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.534+306G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436665 | |||||||
| chr4:185436709 | C | CAATAATA others(2): Show |
4 | a0001c0001t0001g0045 a0001c0001t0001g0140 a0001c0001t0001g0174 others(1): Show |
4 | HG00323.hp1 HG01071.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+352_534+353ins others(9): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436709 | ||||||
| chr4:185436709 | C | CTAATAAT others(3): Show |
1 | a0001c0001t0001g0233 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.534+350_534+351ins others(10): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436709 | |||||||
| chr4:185436712 | A | AAAT | 42 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0019 others(39): Show |
57 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.534+384_534+386dup others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | ||||||
| chr4:185436712 | A | AAATAAT | 32 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(29): Show |
41 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.534+381_534+386dup others(6): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | ||||||
| chr4:185436712 | A | AAATAATA others(2): Show |
41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0034 others(38): Show |
53 | HG00438.hp2 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.534+378_534+386dup others(9): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | ||||||
| chr4:185436712 | A | AAATAATA others(5): Show |
30 | a0001c0001t0001g0012 a0001c0001t0001g0106 a0001c0001t0001g0119 others(27): Show |
35 | HG01071.hp2 HG01074.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.534+375_534+386dup others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | ||||||
| chr4:185436712 | A | AAATAATA others(8): Show |
59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(56): Show |
84 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.534+372_534+386dup others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | ||||||
| chr4:185436712 | A | AAATAATA others(11): Show |
4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0237 others(1): Show |
4 | HG02080.hp2 HG02486.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+369_534+386dup others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | ||||||
| chr4:185436712 | A | AAATAATA others(14): Show |
1 | a0001c0001t0001g0149 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.534+366_534+386dup others(21): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | ||||||
| chr4:185436712 | A | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0140 a0001c0001t0001g0174 others(2): Show |
5 | HG00323.hp1 HG01071.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+353A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436712 | |||||||
| chr4:185436712 | AAAT | A | 14 | a0001c0001t0001g0124 a0001c0001t0001g0227 a0001c0001t0001g0229 others(11): Show |
20 | HG00544.hp1 HG00642.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.534+384_534+386del others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185436712 | ||||||
| chr4:185436746 | T | A | 2 | a0001c0004t0001g0195 a0001c0004t0007g0039 |
3 | HG01884.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.534+387T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436746 | |||||||
| chr4:185436747 | C | T | 2 | a0001c0004t0001g0195 a0001c0004t0007g0039 |
3 | HG01884.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.534+388C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436747 | |||||||
| chr4:185436749 | C | A | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+390C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436749 | |||||||
| chr4:185436775 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.534+416A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436775 | |||||||
| chr4:185436903 | C | T | 1 | a0001c0001t0004g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.534+544C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436903 | |||||||
| chr4:185436998 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.534+639G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185436998 | |||||||
| chr4:185437103 | G | A | 5 | a0002c0002t0001g0048 a0002c0002t0001g0069 a0002c0002t0001g0086 others(2): Show |
5 | HG00639.hp1 HG01106.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+744G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437103 | |||||||
| chr4:185437157 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.534+798T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437157 | |||||||
| chr4:185437163 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.534+804C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437163 | |||||||
| chr4:185437231 | A | T | 14 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0002t0001g0028 others(11): Show |
18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+872A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437231 | |||||||
| chr4:185437307 | C | T | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.534+948C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437307 | |||||||
| chr4:185437308 | G | A | 9 | a0001c0001t0001g0041 a0001c0001t0001g0112 a0001c0001t0001g0213 others(6): Show |
11 | HG00733.hp2 HG01884.hp1 HG03471.hp2 others(8): Show |
intron_variant | MODIFIER | c.534+949G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437308 | |||||||
| chr4:185437360 | A | G | 15 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0112 others(12): Show |
18 | HG02698.hp1 HG02738.hp1 HG04184.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+1001A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437360 | |||||||
| chr4:185437449 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.534+1090C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437449 | |||||||
| chr4:185437481 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.534+1122A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437481 | |||||||
| chr4:185437714 | T | C | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.534+1355T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437714 | |||||||
| chr4:185437716 | T | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.534+1357T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437716 | |||||||
| chr4:185437717 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.534+1358G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437717 | |||||||
| chr4:185437976 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.534+1617C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437976 | |||||||
| chr4:185437988 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0112 a0001c0001t0001g0214 |
4 | NA18998.hp2 NA19000.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+1629C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185437988 | |||||||
| chr4:185438003 | C | CT | 22 | a0001c0001t0001g0003 a0001c0001t0001g0201 a0001c0001t0001g0202 others(19): Show |
32 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.534+1653dupT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185438003 | ||||||
| chr4:185438067 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.534+1708T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438067 | |||||||
| chr4:185438341 | A | G | 4 | a0001c0001t0002g0022 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
5 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.534+1982A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438341 | |||||||
| chr4:185438353 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.534+1994G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438353 | |||||||
| chr4:185438418 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.534+2059C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438418 | |||||||
| chr4:185438435 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0229 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.534+2076T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438435 | |||||||
| chr4:185438480 | G | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0153 a0001c0001t0001g0238 |
3 | NA18612.hp2 NA18966.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.535-2060G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438480 | |||||||
| chr4:185438491 | T | C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0201 a0001c0001t0001g0202 others(19): Show |
32 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.535-2049T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438491 | |||||||
| chr4:185438647 | G | A | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-1893G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438647 | |||||||
| chr4:185438659 | A | G | 4 | a0001c0004t0001g0111 a0001c0004t0001g0194 a0001c0004t0001g0195 others(1): Show |
5 | HG00733.hp2 HG01884.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.535-1881A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438659 | |||||||
| chr4:185438681 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.535-1859A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438681 | |||||||
| chr4:185438703 | G | T | 46 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0224 others(43): Show |
62 | HG00544.hp1 HG00642.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.535-1837G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438703 | |||||||
| chr4:185438732 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.535-1808C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438732 | |||||||
| chr4:185438736 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.535-1804T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438736 | |||||||
| chr4:185438739 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0162 |
2 | HG00597.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.535-1801A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438739 | |||||||
| chr4:185438741 | T | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.535-1799T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438741 | |||||||
| chr4:185438807 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0065 |
3 | HG02922.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.535-1733C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438807 | |||||||
| chr4:185438837 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.535-1703G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438837 | |||||||
| chr4:185438966 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.535-1574T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185438966 | |||||||
| chr4:185439005 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.535-1535C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439005 | |||||||
| chr4:185439012 | G | C | 29 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(26): Show |
36 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.535-1528G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439012 | |||||||
| chr4:185439221 | G | T | 16 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(13): Show |
21 | HG00544.hp1 HG02040.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.535-1319G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439221 | |||||||
| chr4:185439520 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.535-1020T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439520 | |||||||
| chr4:185439724 | A | T | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.535-816A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439724 | |||||||
| chr4:185439727 | CAT | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0267 |
4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-812_535-811del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185439727 | |||||||
| chr4:185439813 | A | ACT | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.535-725_535-724dup others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185439813 | ||||||
| chr4:185439945 | CAT | C | 19 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0002t0001g0028 others(16): Show |
23 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.535-588_535-587del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185439945 | ||||||
| chr4:185439989 | TATATACA others(1): Show |
T | 2 | a0001c0001t0001g0027 a0001c0001t0002g0083 |
3 | HG02055.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.535-546_535-539del others(8): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185439989 | ||||||
| chr4:185440006 | TATAG | T | 7 | a0003c0003t0001g0030 a0003c0003t0001g0051 a0003c0003t0001g0056 others(4): Show |
8 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.535-530_535-527del others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185440006 | ||||||
| chr4:185440010 | G | GATAC | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.535-527_535-526ins others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 185440010 | ||||||
| chr4:185440243 | C | G | 16 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(13): Show |
21 | HG00544.hp1 HG02040.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.535-297C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 5/7 | chr4 | 185440243 | |||||||
| chr4:185440720 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp2 | splice_donor_variant&intron_variant | HIGH | c.714+1G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440720 | |||||||
| chr4:185440722 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
splice_region_variant&intron_variant | LOW | c.714+3A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440722 | |||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0239 a0001c0001t0001g0240 others(1): Show |
5 | HG01123.hp1 HG01192.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(295): Show |
12 | a0001c0001t0001g0124 a0001c0001t0001g0229 a0001c0001t0003g0199 others(9): Show |
19 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(295): Show |
1 | a0001c0001t0004g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
9 | a0002c0002t0001g0009 a0002c0002t0001g0048 a0002c0002t0001g0069 others(6): Show |
11 | HG00639.hp1 HG00733.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(295): Show |
30 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(27): Show |
39 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0002g0223 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
3 | a0001c0001t0006g0125 a0001c0001t0006g0230 a0001c0001t0006g0248 |
3 | HG01099.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(295): Show |
1 | a0004c0011t0001g0258 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0002g0266 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0237 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
3 | a0001c0001t0001g0121 a0001c0001t0001g0153 a0001c0001t0001g0238 |
3 | NA18612.hp2 NA18966.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0007c0008t0001g0137 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0179 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0182 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0036 | 2 | HG00621.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(295): Show |
18 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0041 others(15): Show |
27 | HG00408.hp1 HG00544.hp2 HG02523.hp2 others(24): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
5 | a0001c0001t0001g0102 a0001c0001t0001g0131 a0001c0001t0001g0134 others(2): Show |
5 | NA18966.hp2 NA19007.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
4 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0151 others(1): Show |
4 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0002c0002t0001g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
9 | a0002c0002t0001g0025 a0002c0002t0001g0028 a0002c0002t0001g0055 others(6): Show |
11 | HG01081.hp2 HG01255.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(296): Show |
1 | a0001c0001t0001g0228 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(301): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440758 | T | TAAAGAAA others(295): Show |
1 | a0001c0001t0002g0226 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.714+51_714+52insGC others(300): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440758 | ||||||
| chr4:185440765 | A | G | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.714+46A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440765 | |||||||
| chr4:185440818 | T | C | 1 | a0003c0003t0001g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.714+99T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440818 | |||||||
| chr4:185440822 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.714+103T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185440822 | |||||||
| chr4:185440956 | AT | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.714+249delT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185440956 | ||||||
| chr4:185441079 | T | C | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+360T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441079 | |||||||
| chr4:185441311 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714+592T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441311 | |||||||
| chr4:185441333 | T | C | 1 | a0002c0002t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.714+614T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441333 | |||||||
| chr4:185441340 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.714+621G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441340 | |||||||
| chr4:185441380 | ATATCT | A | 31 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(28): Show |
38 | HG00544.hp1 HG00733.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.714+665_714+669del others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185441380 | ||||||
| chr4:185441419 | CTTGTT | C | 21 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(18): Show |
24 | HG00423.hp1 HG00621.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.714+706_714+710del others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185441419 | ||||||
| chr4:185441510 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.714+791A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441510 | |||||||
| chr4:185441514 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.714+795A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441514 | |||||||
| chr4:185441565 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.714+846G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441565 | |||||||
| chr4:185441609 | C | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0170 a0001c0001t0001g0180 |
3 | HG02602.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.714+890C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185441609 | |||||||
| chr4:185442418 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.714+1699T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442418 | |||||||
| chr4:185442423 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.714+1704T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442423 | |||||||
| chr4:185442545 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.714+1826C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442545 | |||||||
| chr4:185442560 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.714+1841C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442560 | |||||||
| chr4:185442738 | C | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.714+2019C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442738 | |||||||
| chr4:185442864 | A | G | 46 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0224 others(43): Show |
62 | HG00544.hp1 HG00642.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-2100A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442864 | |||||||
| chr4:185442946 | G | A | 6 | a0001c0001t0003g0038 a0001c0001t0003g0122 a0001c0001t0003g0129 others(3): Show |
7 | HG01123.hp2 HG01255.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-2018G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185442946 | |||||||
| chr4:185443017 | A | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0041 others(14): Show |
26 | HG00408.hp1 HG00544.hp2 HG02523.hp2 others(23): Show |
intron_variant | MODIFIER | c.715-1947A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443017 | |||||||
| chr4:185443138 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.715-1826G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443138 | |||||||
| chr4:185443192 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.715-1772A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443192 | |||||||
| chr4:185443320 | G | GTATATAT others(3): Show |
1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.715-1630_715-1621d others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | ||||||
| chr4:185443320 | G | GTATATAT others(5): Show |
4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0175 others(1): Show |
4 | HG02155.hp1 NA19007.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1632_715-1621d others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | ||||||
| chr4:185443320 | G | GTATATAT others(11): Show |
1 | a0001c0001t0004g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.715-1638_715-1621d others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | ||||||
| chr4:185443320 | G | GTATATAT others(13): Show |
1 | a0001c0001t0004g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.715-1640_715-1621d others(22): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | ||||||
| chr4:185443320 | G | GTATATAT others(17): Show |
1 | a0001c0001t0004g0200 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(26): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | ||||||
| chr4:185443320 | GTATA | G | 10 | a0001c0001t0001g0036 a0001c0001t0001g0127 a0001c0001t0001g0128 others(7): Show |
11 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.715-1624_715-1621d others(6): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | ||||||
| chr4:185443320 | GTATATA | G | 4 | a0001c0001t0001g0157 a0001c0001t0001g0237 a0001c0001t0001g0243 others(1): Show |
4 | HG02132.hp2 NA18612.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1626_715-1621d others(8): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443320 | ||||||
| chr4:185443322 | A | G | 6 | a0002c0002t0001g0048 a0002c0002t0001g0069 a0002c0002t0001g0086 others(3): Show |
6 | HG00639.hp1 HG01106.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-1642A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443322 | |||||||
| chr4:185443332 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.715-1632A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443332 | |||||||
| chr4:185443333 | TATATA | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0236 others(5): Show |
8 | HG01123.hp1 HG01192.hp2 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-1630_715-1626d others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443333 | |||||||
| chr4:185443334 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0202 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.715-1629_715-1628i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443334 | ||||||
| chr4:185443334 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.715-1630A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443334 | |||||||
| chr4:185443336 | A | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0210 |
2 | HG02523.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.715-1628A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443336 | |||||||
| chr4:185443338 | A | T | 8 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0202 others(5): Show |
8 | HG00621.hp2 HG00735.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-1626A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443338 | |||||||
| chr4:185443338 | ATATATT | A | 11 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0002t0001g0028 others(8): Show |
15 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.715-1624_715-1619d others(8): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443338 | ||||||
| chr4:185443340 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0016 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.715-1623_715-1622i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443340 | ||||||
| chr4:185443340 | A | T | 26 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(23): Show |
27 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.715-1624A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443340 | |||||||
| chr4:185443340 | ATATTTT | A | 6 | a0002c0002t0001g0048 a0002c0002t0001g0069 a0002c0002t0001g0086 others(3): Show |
6 | HG00639.hp1 HG01106.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-1622_715-1617d others(8): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443340 | ||||||
| chr4:185443342 | A | ATATATAT others(4): Show |
6 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0102 others(3): Show |
6 | HG01358.hp2 HG02129.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(18): Show |
1 | a0001c0001t0004g0015 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(27): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(22): Show |
1 | a0001c0001t0004g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(31): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(26): Show |
1 | a0001c0001t0004g0193 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(35): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0203 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(45): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(35): Show |
1 | a0001c0001t0001g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(44): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0016 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(46): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(22): Show |
1 | a0001c0001t0004g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(31): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0207 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(40): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0209 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(42): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(18): Show |
1 | a0001c0001t0004g0005 | 2 | HG01975.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(27): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(20): Show |
1 | a0001c0001t0004g0005 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(29): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0204 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(37): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0206 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(38): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0115 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(33): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0215 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(36): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0214 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(38): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(14): Show |
1 | a0001c0004t0001g0194 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(23): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0212 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(24): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0213 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(36): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(28): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0112 |
2 | NA18998.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(37): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(11): Show |
2 | a0001c0001t0003g0199 a0001c0001t0004g0015 |
3 | HG02572.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0001 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(22): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0041 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(37): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0251 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(19): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0109 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0141 a0001c0001t0001g0169 |
4 | HG00408.hp2 HG00741.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0233 |
2 | NA18999.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0245 a0001c0001t0003g0185 |
2 | HG01975.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(7): Show |
9 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0037 others(6): Show |
9 | HG00099.hp2 HG01099.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(16): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
2 | HG00738.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0110 a0001c0001t0006g0248 |
2 | HG01099.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0104 a0001c0001t0001g0151 a0001c0001t0006g0125 others(1): Show |
4 | HG02055.hp1 HG02486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(19): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0201 |
4 | NA18952.hp1 NA18959.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(28): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0003 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(29): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0136 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(4): Show |
12 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0116 others(9): Show |
12 | HG00639.hp2 HG01071.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(5): Show |
37 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(34): Show |
43 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0147 |
2 | NA19056.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(7): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0148 others(5): Show |
8 | HG01258.hp2 HG01433.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(16): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0108 a0001c0001t0001g0133 |
2 | HG01081.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(9): Show |
1 | a0001c0004t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0003 | 2 | NA18955.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(28): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0139 a0001c0001t0002g0018 a0001c0001t0002g0226 others(2): Show |
5 | HG00438.hp1 HG01071.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0004 a0001c0001t0001g0118 a0001c0001t0001g0126 others(6): Show |
9 | HG01256.hp1 HG01496.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(5): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(5): Show |
11 | HG00423.hp2 HG02280.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(6): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0143 others(1): Show |
4 | HG02738.hp2 HG04184.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(7): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0160 others(2): Show |
5 | HG01074.hp2 HG01516.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(16): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(8): Show |
1 | a0001c0004t0001g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(9): Show |
1 | a0001c0004t0007g0039 | 2 | HG01884.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0003 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(24): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATTT others(1): Show |
7 | a0001c0001t0001g0227 a0001c0001t0001g0271 a0001c0001t0002g0021 others(4): Show |
8 | HG00544.hp1 HG03654.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(10): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATTT others(3): Show |
1 | a0001c0001t0003g0159 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATTT others(4): Show |
5 | a0001c0001t0001g0149 a0001c0001t0001g0158 a0001c0001t0001g0164 others(2): Show |
5 | HG00735.hp1 HG04228.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATTT others(5): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(3): Show |
7 | HG00738.hp2 HG02040.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATATTT others(6): Show |
1 | a0001c0001t0001g0011 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATGTAT others(54): Show |
1 | a0001c0001t0001g0016 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(63): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATTTTT others(3): Show |
1 | a0001c0001t0001g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0229 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATTTTT others(5): Show |
4 | a0001c0001t0001g0153 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | NA18612.hp2 NA18966.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATATTTTT others(6): Show |
1 | a0001c0001t0001g0105 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.715-1621_715-1620i others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATTTTT | 6 | a0001c0001t0001g0043 a0001c0001t0001g0259 a0001c0001t0001g0260 others(3): Show |
7 | HG01884.hp2 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-1607_715-1603d others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | ATTTTTTT others(3): Show |
1 | a0004c0011t0001g0258 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.715-1612_715-1603d others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | A | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0042 others(27): Show |
32 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.715-1622A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443342 | |||||||
| chr4:185443342 | AT | A | 20 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(17): Show |
24 | HG00140.hp2 HG00741.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.715-1603delT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443342 | ATT | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0067 others(3): Show |
8 | HG02145.hp1 HG02257.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-1604_715-1603d others(4): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443342 | ||||||
| chr4:185443343 | T | TA | 5 | a0001c0001t0001g0065 a0001c0001t0001g0076 a0001c0001t0001g0096 others(2): Show |
5 | HG01192.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-1621_715-1620i others(3): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443343 | |||||||
| chr4:185443343 | T | TATATATA others(14): Show |
1 | a0001c0001t0004g0032 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(23): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443343 | |||||||
| chr4:185443343 | T | TATATATA others(16): Show |
3 | a0001c0001t0004g0032 a0001c0001t0004g0040 a0001c0001t0004g0113 |
3 | HG00642.hp1 HG03209.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.715-1621_715-1620i others(25): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443343 | |||||||
| chr4:185443343 | T | TATATATA others(18): Show |
1 | a0001c0001t0004g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.715-1621_715-1620i others(27): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443343 | |||||||
| chr4:185443344 | T | A | 5 | a0001c0001t0001g0063 a0001c0001t0004g0198 a0003c0003t0001g0051 others(2): Show |
5 | HG02257.hp1 HG02976.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-1620T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443344 | |||||||
| chr4:185443345 | T | A | 7 | a0001c0001t0001g0065 a0001c0001t0001g0075 a0001c0001t0001g0076 others(4): Show |
7 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-1619T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443345 | |||||||
| chr4:185443346 | T | A | 1 | a0001c0001t0002g0020 | 3 | HG02145.hp1 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.715-1618T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443346 | |||||||
| chr4:185443347 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.715-1617T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443347 | |||||||
| chr4:185443374 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.715-1590T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443374 | |||||||
| chr4:185443451 | C | T | 11 | a0001c0001t0003g0199 a0001c0001t0004g0005 a0001c0001t0004g0015 others(8): Show |
18 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.715-1513C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443451 | |||||||
| chr4:185443589 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.715-1375T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443589 | |||||||
| chr4:185443593 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.715-1371C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443593 | |||||||
| chr4:185443597 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.715-1367A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443597 | |||||||
| chr4:185443598 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.715-1366T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443598 | |||||||
| chr4:185443601 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.715-1363G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443601 | |||||||
| chr4:185443676 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.715-1288G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443676 | |||||||
| chr4:185443739 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.715-1225T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443739 | |||||||
| chr4:185443776 | A | G | 1 | a0001c0001t0003g0103 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.715-1188A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443776 | |||||||
| chr4:185443913 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.715-1051A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443913 | |||||||
| chr4:185443921 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0070 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.715-1010_715-1000d others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0080 a0001c0001t0001g0097 |
2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.715-1016_715-1000d others(19): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0081 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.715-1017_715-1000d others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTT | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0078 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-1004_715-1000d others(7): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.715-1009_715-1000d others(12): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0049 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.715-1010_715-1000d others(13): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0001g0194 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.715-1011_715-1000d others(14): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0077 a0001c0010t0001g0053 a0003c0003t0001g0051 others(1): Show |
4 | HG00741.hp1 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1012_715-1000d others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(7): Show |
C | 24 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0135 others(21): Show |
27 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.715-1013_715-1000d others(16): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(8): Show |
C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
154 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.715-1014_715-1000d others(17): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(9): Show |
C | 8 | a0001c0001t0001g0124 a0001c0001t0001g0128 a0001c0001t0001g0142 others(5): Show |
8 | HG00099.hp2 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-1015_715-1000d others(18): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(10): Show |
C | 14 | a0001c0001t0001g0229 a0001c0001t0003g0199 a0001c0001t0004g0005 others(11): Show |
21 | HG00642.hp1 HG01433.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.715-1016_715-1000d others(19): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(11): Show |
C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0202 others(18): Show |
32 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.715-1017_715-1000d others(20): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(12): Show |
C | 5 | a0001c0001t0001g0201 a0001c0001t0002g0020 a0001c0001t0002g0219 others(2): Show |
7 | HG01109.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-1018_715-1000d others(21): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(13): Show |
C | 29 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(26): Show |
37 | HG00544.hp1 HG01884.hp2 HG02040.hp1 others(34): Show |
intron_variant | MODIFIER | c.715-1019_715-1000d others(22): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0001g0271 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.715-1020_715-1000d others(23): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(15): Show |
C | 4 | a0001c0001t0001g0209 a0001c0004t0001g0111 a0001c0004t0001g0195 others(1): Show |
5 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-1021_715-1000d others(24): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(16): Show |
C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0112 others(8): Show |
14 | HG02698.hp1 HG02738.hp1 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.715-1022_715-1000d others(25): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(17): Show |
C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0213 |
2 | NA18973.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.715-1023_715-1000d others(26): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443921 | CTTTTTTT others(18): Show |
C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0066 |
4 | HG01243.hp1 NA18990.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1024_715-1000d others(27): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185443921 | ||||||
| chr4:185443925 | T | C | 2 | a0003c0003t0001g0056 a0003c0003t0002g0068 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.715-1039T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443925 | |||||||
| chr4:185443927 | T | C | 1 | a0003c0003t0002g0057 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.715-1037T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443927 | |||||||
| chr4:185443928 | T | C | 1 | a0003c0003t0002g0084 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.715-1036T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443928 | |||||||
| chr4:185443944 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0267 |
4 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-1020T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443944 | |||||||
| chr4:185443978 | G | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.715-986G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443978 | |||||||
| chr4:185443985 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.715-979T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443985 | |||||||
| chr4:185443995 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.715-969G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185443995 | |||||||
| chr4:185444039 | C | T | 2 | a0001c0004t0001g0194 a0001c0010t0001g0053 |
2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.715-925C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444039 | |||||||
| chr4:185444047 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0065 a0001c0001t0004g0113 |
4 | HG02922.hp1 HG03453.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-917G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444047 | |||||||
| chr4:185444110 | C | T | 1 | a0001c0001t0004g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.715-854C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444110 | |||||||
| chr4:185444143 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0095 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.715-821C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444143 | |||||||
| chr4:185444155 | T | G | 2 | a0002c0002t0001g0073 a0002c0002t0001g0269 |
2 | HG01081.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.715-809T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444155 | |||||||
| chr4:185444205 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0112 a0001c0001t0001g0213 others(2): Show |
6 | NA18954.hp1 NA18998.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-759G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444205 | |||||||
| chr4:185444340 | C | G | 1 | a0001c0001t0001g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.715-624C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444340 | |||||||
| chr4:185444454 | T | C | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-510T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444454 | |||||||
| chr4:185444495 | A | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.715-469A>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444495 | |||||||
| chr4:185444510 | T | A | 1 | a0001c0004t0001g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-454T>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444510 | |||||||
| chr4:185444569 | GACTGGCA others(8): Show |
G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.715-391_715-377del others(15): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 185444569 | ||||||
| chr4:185444688 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.715-276A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444688 | |||||||
| chr4:185444844 | G | A | 33 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(30): Show |
42 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.715-120G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444844 | |||||||
| chr4:185444871 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.715-93C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444871 | |||||||
| chr4:185444947 | C | T | 14 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0002t0001g0028 others(11): Show |
18 | HG00733.hp1 HG01074.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.715-17C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 6/7 | chr4 | 185444947 | |||||||
| chr4:185445161 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.881+31T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445161 | |||||||
| chr4:185445199 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.881+69A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445199 | |||||||
| chr4:185445228 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.881+98T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445228 | |||||||
| chr4:185445264 | T | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0170 a0001c0001t0001g0180 |
3 | HG02602.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.881+134T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445264 | |||||||
| chr4:185445461 | G | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0227 others(30): Show |
42 | HG00544.hp1 HG01109.hp2 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.881+331G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445461 | |||||||
| chr4:185445517 | A | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0112 others(11): Show |
17 | HG02698.hp1 HG02738.hp1 HG04199.hp1 others(14): Show |
intron_variant | MODIFIER | c.881+387A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445517 | |||||||
| chr4:185445655 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.881+525C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445655 | |||||||
| chr4:185445864 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.881+734G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445864 | |||||||
| chr4:185445878 | A | T | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+748A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185445878 | |||||||
| chr4:185446040 | C | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0251 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.881+910C>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446040 | |||||||
| chr4:185446065 | T | G | 1 | a0001c0001t0003g0159 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.881+935T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446065 | |||||||
| chr4:185446075 | A | G | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881+945A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446075 | |||||||
| chr4:185446121 | G | A | 2 | a0003c0003t0001g0051 a0003c0003t0001g0060 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.881+991G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446121 | |||||||
| chr4:185446297 | A | T | 1 | a0002c0002t0001g0058 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.881+1167A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446297 | |||||||
| chr4:185446358 | A | G | 1 | a0002c0002t0001g0087 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.881+1228A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446358 | |||||||
| chr4:185446588 | C | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.881+1458C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446588 | |||||||
| chr4:185446711 | A | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0201 a0001c0001t0001g0202 others(20): Show |
33 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.881+1581A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446711 | |||||||
| chr4:185446721 | CACA | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.881+1595_881+1597d others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185446721 | ||||||
| chr4:185446932 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.881+1802C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446932 | |||||||
| chr4:185446956 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.881+1826A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185446956 | |||||||
| chr4:185447136 | G | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0112 others(11): Show |
17 | HG02698.hp1 HG02738.hp1 HG04199.hp1 others(14): Show |
intron_variant | MODIFIER | c.881+2006G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447136 | |||||||
| chr4:185447186 | CT | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.881+2069delT | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185447186 | ||||||
| chr4:185447187 | T | C | 13 | a0001c0001t0001g0124 a0001c0001t0001g0229 a0001c0001t0003g0199 others(10): Show |
20 | HG00642.hp1 HG01934.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.881+2057T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447187 | |||||||
| chr4:185447212 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.881+2082C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447212 | |||||||
| chr4:185447213 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(230): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.881+2083A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447213 | |||||||
| chr4:185447233 | A | G | 5 | a0001c0001t0002g0021 a0001c0001t0002g0220 a0001c0001t0002g0225 others(2): Show |
6 | HG00639.hp1 HG01106.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+2103A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447233 | |||||||
| chr4:185447268 | A | G | 6 | a0001c0001t0001g0152 a0001c0001t0001g0164 a0001c0001t0001g0245 others(3): Show |
6 | HG00423.hp1 HG00639.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+2138A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447268 | |||||||
| chr4:185447272 | G | C | 6 | a0001c0001t0001g0152 a0001c0001t0001g0164 a0001c0001t0001g0245 others(3): Show |
6 | HG00423.hp1 HG00639.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.881+2142G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447272 | |||||||
| chr4:185447331 | G | A | 2 | a0001c0001t0006g0125 a0001c0001t0006g0230 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.881+2201G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447331 | |||||||
| chr4:185447338 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.881+2208C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447338 | |||||||
| chr4:185447381 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.882-2215T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447381 | |||||||
| chr4:185447388 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.882-2208G>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447388 | |||||||
| chr4:185447393 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0251 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.882-2203G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447393 | |||||||
| chr4:185447398 | A | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0251 a0001c0001t0003g0155 |
3 | HG01981.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.882-2198A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447398 | |||||||
| chr4:185447401 | T | C | 3 | a0001c0001t0001g0245 a0001c0001t0001g0251 a0001c0001t0003g0155 |
3 | HG01981.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.882-2195T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447401 | |||||||
| chr4:185447416 | G | A | 1 | a0001c0001t0003g0155 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.882-2180G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447416 | |||||||
| chr4:185447539 | C | T | 3 | a0001c0001t0001g0082 a0002c0002t0001g0072 a0002c0002t0001g0090 |
3 | HG03195.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.882-2057C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447539 | |||||||
| chr4:185447655 | T | TG | 43 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(40): Show |
51 | HG00140.hp2 HG00741.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.882-1940dupG | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185447655 | ||||||
| chr4:185447964 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0224 a0001c0001t0001g0263 |
5 | HG02074.hp2 HG02083.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.882-1632A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185447964 | |||||||
| chr4:185448015 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0251 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.882-1581G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448015 | |||||||
| chr4:185448024 | T | G | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-1572T>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448024 | |||||||
| chr4:185448089 | C | T | 1 | a0002c0002t0001g0058 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.882-1507C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448089 | |||||||
| chr4:185448227 | G | C | 1 | a0001c0010t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882-1369G>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448227 | |||||||
| chr4:185448255 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.882-1341A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448255 | |||||||
| chr4:185448263 | C | T | 1 | a0001c0001t0003g0185 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.882-1333C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448263 | |||||||
| chr4:185448426 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0064 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.882-1170A>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448426 | |||||||
| chr4:185448544 | C | G | 1 | a0002c0002t0001g0092 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.882-1052C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448544 | |||||||
| chr4:185448691 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.882-905C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448691 | |||||||
| chr4:185448864 | G | GCATAT | 44 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(41): Show |
52 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.882-732_882-731ins others(5): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448864 | |||||||
| chr4:185448866 | A | T | 44 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(41): Show |
52 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.882-730A>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448866 | |||||||
| chr4:185448867 | C | G | 44 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(41): Show |
52 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.882-729C>G | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448867 | |||||||
| chr4:185448955 | G | A | 3 | a0001c0004t0001g0111 a0001c0004t0001g0195 a0001c0004t0007g0039 |
4 | HG01884.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-641G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448955 | |||||||
| chr4:185448962 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.882-634C>T | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185448962 | |||||||
| chr4:185448962 | CTT | C | 44 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(41): Show |
52 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.882-632_882-631del others(2): Show |
C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185448962 | ||||||
| chr4:185449210 | T | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(100): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.882-386T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185449210 | |||||||
| chr4:185449413 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.882-183T>C | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185449413 | |||||||
| chr4:185449522 | T | TA | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(142): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.882-62dupA | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 185449522 | ||||||
| chr4:185449573 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0201 others(8): Show |
17 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.882-23G>A | C4orf47 | ENSG00000205129.9 | transcript | ENST00000378850.5 | protein_coding | 7/7 | chr4 | 185449573 |