Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10898 |
| ensemblid | ENSG00000160917.15 |
| hgncid | 2327 |
| symbol | CPSF4 |
| name | cleavage and polyadenylation specific factor 4 |
| refseq_nuc | NM_006693.4 |
| refseq_prot | NP_006684.1 |
| ensembl_nuc | ENST00000292476.10 |
| ensembl_prot | ENSP00000292476.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 99438943 |
| end | 99457373 |
| strand | + |
| ver | v1.2 |
| region | chr7:99438943-99457373 |
| region5000 | chr7:99433943-99462373 |
| regionname0 | CPSF4_chr7_99438943_99457373 |
| regionname5000 | CPSF4_chr7_99433943_99462373 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 807 | 166 | 62 | 15 | 64 | 5 | 20 | CPSF4_chr7_99433943_99462373 | CPSF4 | ATGCA others(802): Show |
chr7 | 99433943 | 99462373 | ||
| a0001c0002 | 1/1 | 807 | 166 | 9 | 46 | 81 | 10 | 18 | CPSF4_chr7_99433943_99462373 | CPSF4 | ATGCA others(802): Show |
chr7 | 99433943 | 99462373 | ||
| a0001c0003 | 0/0 | 807 | 31 | 21 | 2 | 7 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | ATGCA others(802): Show |
chr7 | 99433943 | 99462373 | ||
| a0001c0004 | 0/0 | 807 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | ATGCA others(802): Show |
chr7 | 99433943 | 99462373 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 1823 | 63 | 46 | 10 | 1 | 4 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0001t0003 | 0/0 | 1823 | 94 | 7 | 5 | 63 | 1 | 18 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0001t0004 | 0/0 | 1823 | 5 | 5 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0001t0007 | 0/0 | 1823 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0001t0010 | 0/0 | 1823 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0002t0001 | 1/1 | 1823 | 154 | 5 | 43 | 77 | 10 | 17 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0002t0002 | 0/0 | 1823 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0002t0005 | 0/0 | 1823 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0002t0006 | 0/0 | 1823 | 3 | 1 | 2 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0002t0008 | 0/0 | 1823 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0002t0011 | 0/0 | 1823 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0002t0013 | 0/0 | 1823 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0003t0002 | 0/0 | 1823 | 29 | 21 | 1 | 6 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0003t0009 | 0/0 | 1823 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0003t0012 | 0/0 | 1823 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| a0001c0004t0001 | 0/0 | 1823 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | GGCAT others(1818): Show |
chr7 | 99433943 | 99462373 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0014 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0002 | 0/0 | 11 | 2 | 0 | 7 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0004 | 0/0 | 10 | 2 | 0 | 5 | 0 | 3 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0007 | 0/0 | 7 | 0 | 2 | 3 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0001t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0001 | 0/0 | 10 | 1 | 2 | 5 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0003 | 1/0 | 9 | 0 | 3 | 4 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0005 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0006 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0010 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0005g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0006g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0008g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0011g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0002t0013g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0009g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0003t0012g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| a0001c0004t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0024 | EUR | GBR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0103 | EUR | GBR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | FIN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0231 | EUR | FIN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | FIN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0030 | EUR | FIN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | CHS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00733 | hp2 | a0001 | c0002 | t0006 | g0032 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00735 | hp1 | a0001 | c0002 | t0008 | g0176 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0092 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01175 | hp2 | a0001 | c0003 | t0009 | g0097 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01192 | hp2 | a0001 | c0004 | t0001 | g0150 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01358 | hp2 | a0001 | c0002 | t0006 | g0011 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0211 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0145 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0122 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0215 | EUR | IBS | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0201 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0114 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0108 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0214 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | CDX | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02165 | hp2 | a0001 | c0002 | t0011 | g0003 | EAS | CDX | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0105 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0111 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0001 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02523 | hp2 | a0001 | c0003 | t0002 | g0093 | EAS | KHV | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0089 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0102 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0106 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0112 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0195 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02970 | hp1 | a0001 | c0003 | t0002 | g0101 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0094 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0083 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0087 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0023 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03490 | hp1 | a0001 | c0002 | t0013 | g0030 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0115 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0107 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0109 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0147 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0243 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | BEB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | STU | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0113 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | CHB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0088 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18939 | hp1 | a0001 | c0003 | t0002 | g0099 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18943 | hp2 | a0001 | c0002 | t0005 | g0011 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0248 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18982 | hp1 | a0001 | c0002 | t0005 | g0033 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18989 | hp1 | a0001 | c0003 | t0012 | g0200 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18989 | hp2 | a0001 | c0003 | t0002 | g0095 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0096 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | LWK | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | LWK | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | LWK | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | LWK | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19054 | hp2 | a0001 | c0003 | t0002 | g0098 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19062 | hp1 | a0001 | c0002 | t0005 | g0033 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0091 | AFR | YRI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | TSI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0152 | EUR | TSI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0205 | EUR | TSI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0032 | EUR | TSI | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | GIH | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | GIH | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0104 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0198 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0023 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0110 | AFR | MSL | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0100 | AFR | USA | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | USA | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | USA | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | USA | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0188 | REF | REF | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0003 | REF | REF | CPSF4_chr7_99433943_99462373 | CPSF4 | chr7 | 99433943 | 99462373 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99450355 | T | C | 2 | a0001c0001 a0001c0003 |
197 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
synonymous_variant | LOW | c.387T>C | p.Arg129Arg | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/8 | 527/1823 | 387/810 | 129/269 | chr7 | 99450355 | |||
| chr7:99450781 | G | A | 1 | a0001c0004 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.483G>A | p.Ser161Ser | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/8 | 623/1823 | 483/810 | 161/269 | chr7 | 99450781 | |||
| chr7:99452416 | G | A | 1 | a0001c0003 | 31 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(28): Show |
synonymous_variant | LOW | c.546G>A | p.Pro182Pro | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/8 | 686/1823 | 546/810 | 182/269 | chr7 | 99452416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99439026 | C | G | 2 | a0001c0001t0003 a0001c0001t0007 |
97 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-57C>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/8 | 57 | chr7 | 99439026 | ||||||
| chr7:99456538 | C | T | 1 | a0001c0002t0013 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 38 | chr7 | 99456538 | ||||||
| chr7:99456640 | G | A | 1 | a0001c0002t0008 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*140G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 140 | chr7 | 99456640 | ||||||
| chr7:99456666 | T | G | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
199 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*166T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 166 | chr7 | 99456666 | ||||||
| chr7:99456737 | G | A | 2 | a0001c0001t0004 a0001c0003t0009 |
6 | HG01175.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*237G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 237 | chr7 | 99456737 | ||||||
| chr7:99456750 | T | A | 2 | a0001c0002t0005 a0001c0002t0011 |
4 | HG02165.hp2 NA18943.hp2 NA18982.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*250T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 250 | chr7 | 99456750 | ||||||
| chr7:99456751 | G | A | 1 | a0001c0001t0007 | 3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*251G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 251 | chr7 | 99456751 | ||||||
| chr7:99456752 | G | A | 2 | a0001c0002t0005 a0001c0002t0011 |
4 | HG02165.hp2 NA18943.hp2 NA18982.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*252G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 252 | chr7 | 99456752 | ||||||
| chr7:99456782 | G | A | 1 | a0001c0001t0004 | 5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*282G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 282 | chr7 | 99456782 | ||||||
| chr7:99456848 | T | C | 1 | a0001c0001t0010 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*348T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 348 | chr7 | 99456848 | ||||||
| chr7:99456869 | C | T | 1 | a0001c0003t0012 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*369C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 369 | chr7 | 99456869 | ||||||
| chr7:99457040 | A | T | 1 | a0001c0002t0006 | 3 | HG00733.hp2 HG01358.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*540A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 540 | chr7 | 99457040 | ||||||
| chr7:99457137 | C | T | 1 | a0001c0002t0011 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 8/8 | 637 | chr7 | 99457137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99439297 | G | A | 50 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0013 others(47): Show |
61 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.103+112G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99439297 | |||||||
| chr7:99439355 | C | T | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+170C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99439355 | |||||||
| chr7:99440204 | C | T | 1 | a0001c0003t0002g0248 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.103+1019C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440204 | |||||||
| chr7:99440360 | T | C | 3 | a0001c0003t0002g0087 a0001c0003t0002g0088 a0001c0003t0002g0089 |
3 | HG02615.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.103+1175T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440360 | |||||||
| chr7:99440378 | G | T | 1 | a0001c0002t0001g0247 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.103+1193G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440378 | |||||||
| chr7:99440417 | T | C | 1 | a0001c0002t0001g0090 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.103+1232T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440417 | |||||||
| chr7:99440434 | G | A | 29 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(26): Show |
30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.103+1249G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440434 | |||||||
| chr7:99440458 | C | T | 5 | a0001c0001t0002g0043 a0001c0001t0002g0068 a0001c0001t0002g0070 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+1273C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440458 | |||||||
| chr7:99440557 | T | G | 1 | a0001c0001t0002g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.103+1372T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440557 | |||||||
| chr7:99440632 | T | C | 34 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(31): Show |
35 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.103+1447T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440632 | |||||||
| chr7:99440651 | CTGGCATA others(16): Show |
C | 3 | a0001c0002t0002g0115 a0001c0002t0002g0116 a0001c0002t0002g0117 |
3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.103+1468_103+1490d others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440651 | ||||||
| chr7:99440653 | G | GGC | 5 | a0001c0003t0002g0023 a0001c0003t0002g0104 a0001c0003t0002g0106 others(2): Show |
6 | HG02055.hp2 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+1469_103+1470d others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440653 | ||||||
| chr7:99440655 | C | CAT | 7 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0011 others(4): Show |
10 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.103+1489_103+1490d others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | ||||||
| chr7:99440655 | C | CATATATA others(1): Show |
3 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0003t0002g0094 |
3 | HG02451.hp2 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.103+1483_103+1490d others(10): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | ||||||
| chr7:99440655 | C | CATATATA others(3): Show |
2 | a0001c0001t0003g0026 a0001c0001t0003g0162 |
2 | HG00621.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.103+1481_103+1490d others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | ||||||
| chr7:99440655 | C | CATATATA others(5): Show |
1 | a0001c0001t0003g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.103+1479_103+1490d others(14): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | ||||||
| chr7:99440655 | C | CATATATA others(13): Show |
1 | a0001c0003t0002g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.103+1471_103+1490d others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | ||||||
| chr7:99440655 | C | CATATATA others(17): Show |
1 | a0001c0003t0002g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(26): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | ||||||
| chr7:99440655 | C | CATATATA others(21): Show |
3 | a0001c0001t0002g0197 a0001c0003t0002g0100 a0001c0003t0002g0101 |
3 | HG02809.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(30): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | ||||||
| chr7:99440655 | C | CGCATATA others(7): Show |
1 | a0001c0003t0002g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.103+1470_103+1471i others(16): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | |||||||
| chr7:99440655 | C | CGCATATA others(9): Show |
3 | a0001c0003t0002g0096 a0001c0003t0002g0099 a0001c0003t0009g0097 |
3 | HG01175.hp2 NA18939.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.103+1470_103+1471i others(18): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | |||||||
| chr7:99440655 | C | CGCATATA others(11): Show |
3 | a0001c0003t0002g0093 a0001c0003t0002g0095 a0001c0003t0002g0248 |
3 | HG02523.hp2 NA18971.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.103+1470_103+1471i others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | |||||||
| chr7:99440655 | C | CGCATATA others(15): Show |
1 | a0001c0003t0002g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.103+1470_103+1471i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | |||||||
| chr7:99440655 | C | CGCATATA others(17): Show |
1 | a0001c0003t0002g0103 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.103+1470_103+1471i others(26): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440655 | |||||||
| chr7:99440655 | CATATATA others(1): Show |
C | 4 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(1): Show |
4 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+1483_103+1490d others(10): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440655 | ||||||
| chr7:99440656 | A | G | 3 | a0001c0003t0002g0087 a0001c0003t0002g0088 a0001c0003t0002g0089 |
3 | HG02615.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.103+1471A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440656 | |||||||
| chr7:99440657 | T | C | 3 | a0001c0003t0002g0087 a0001c0003t0002g0088 a0001c0003t0002g0089 |
3 | HG02615.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.103+1472T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440657 | |||||||
| chr7:99440663 | T | C | 1 | a0001c0001t0003g0004 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.103+1478T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440663 | |||||||
| chr7:99440666 | ATATATAT others(3): Show |
A | 1 | a0001c0003t0002g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.103+1483_103+1492d others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440666 | ||||||
| chr7:99440666 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0002g0084 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103+1483_103+1493d others(13): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440666 | ||||||
| chr7:99440672 | A | T | 1 | a0001c0002t0011g0003 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.103+1487A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440672 | |||||||
| chr7:99440673 | TA | T | 2 | a0001c0002t0001g0003 a0001c0002t0005g0033 |
3 | NA18946.hp1 NA18982.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.103+1489delA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440673 | |||||||
| chr7:99440674 | A | ATATATAT others(18): Show |
1 | a0001c0003t0002g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(56): Show |
1 | a0001c0001t0002g0009 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(65): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(47): Show |
1 | a0001c0001t0002g0050 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(56): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(45): Show |
2 | a0001c0001t0002g0048 a0001c0001t0002g0049 |
2 | HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(54): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(43): Show |
1 | a0001c0001t0002g0065 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(52): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(38): Show |
1 | a0001c0001t0002g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(47): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(36): Show |
1 | a0001c0001t0002g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(45): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(30): Show |
1 | a0001c0003t0002g0113 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(39): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(34): Show |
1 | a0001c0001t0002g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(43): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(32): Show |
1 | a0001c0001t0002g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(41): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(33): Show |
2 | a0001c0001t0002g0059 a0001c0001t0002g0085 |
2 | HG03654.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(42): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(30): Show |
1 | a0001c0003t0002g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(39): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(30): Show |
2 | a0001c0001t0002g0057 a0001c0001t0002g0086 |
2 | HG02257.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(39): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(31): Show |
2 | a0001c0001t0002g0009 a0001c0001t0002g0074 |
2 | HG02083.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(40): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(32): Show |
1 | a0001c0001t0002g0070 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(41): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(22): Show |
1 | a0001c0003t0002g0023 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(31): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(27): Show |
1 | a0001c0001t0002g0199 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(36): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(28): Show |
2 | a0001c0001t0002g0068 a0001c0001t0002g0069 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(37): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(29): Show |
3 | a0001c0001t0002g0043 a0001c0001t0002g0072 a0001c0001t0002g0073 |
3 | HG02109.hp1 HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(38): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(21): Show |
1 | a0001c0003t0002g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(30): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(26): Show |
2 | a0001c0001t0002g0196 a0001c0003t0002g0104 |
2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(35): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(25): Show |
1 | a0001c0001t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(34): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(27): Show |
11 | a0001c0001t0002g0014 a0001c0001t0002g0021 a0001c0001t0002g0047 others(8): Show |
12 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(36): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(28): Show |
1 | a0001c0001t0002g0014 | 2 | HG02145.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(37): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(24): Show |
2 | a0001c0001t0002g0061 a0001c0001t0002g0076 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(33): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(18): Show |
1 | a0001c0003t0002g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(22): Show |
1 | a0001c0003t0002g0107 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(31): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(17): Show |
1 | a0001c0001t0003g0020 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(26): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(21): Show |
1 | a0001c0003t0002g0106 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(30): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(20): Show |
1 | a0001c0001t0002g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(29): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(13): Show |
1 | a0001c0003t0002g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0229 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(28): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0039 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(15): Show |
2 | a0001c0001t0003g0008 a0001c0001t0003g0194 |
2 | NA18947.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(16): Show |
2 | a0001c0001t0003g0002 a0001c0001t0003g0190 |
3 | NA18948.hp2 NA18966.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(10): Show |
1 | a0001c0001t0007g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(19): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(12): Show |
1 | a0001c0001t0003g0242 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(21): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(13): Show |
2 | a0001c0001t0003g0039 a0001c0001t0003g0223 |
2 | NA18982.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(14): Show |
2 | a0001c0001t0003g0007 a0001c0001t0003g0233 |
2 | HG04184.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(15): Show |
4 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0038 others(1): Show |
4 | HG01496.hp2 HG02071.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0007 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(15): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(10): Show |
2 | a0001c0001t0003g0217 a0001c0001t0007g0195 |
2 | HG02818.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(19): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(11): Show |
2 | a0001c0001t0003g0036 a0001c0001t0007g0198 |
2 | HG02559.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(12): Show |
5 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0036 others(2): Show |
5 | NA18944.hp2 NA18980.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(21): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(13): Show |
11 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0008 others(8): Show |
15 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(14): Show |
8 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0008 others(5): Show |
10 | HG02735.hp1 HG02735.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(15): Show |
4 | a0001c0001t0003g0004 a0001c0001t0003g0037 a0001c0001t0003g0042 others(1): Show |
4 | HG02074.hp2 HG02523.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(18): Show |
1 | a0001c0001t0003g0004 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0004 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(15): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(9): Show |
1 | a0001c0001t0003g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(18): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(10): Show |
3 | a0001c0001t0003g0041 a0001c0001t0003g0225 a0001c0001t0003g0243 |
3 | HG03942.hp2 NA18963.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(19): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(11): Show |
2 | a0001c0001t0003g0008 a0001c0001t0003g0037 |
2 | HG02602.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(12): Show |
5 | a0001c0001t0003g0004 a0001c0001t0003g0020 a0001c0001t0003g0042 others(2): Show |
5 | HG00280.hp2 HG02622.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(21): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(13): Show |
6 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(3): Show |
7 | HG01099.hp2 HG02132.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(14): Show |
3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0192 |
3 | NA18956.hp1 NA18969.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(15): Show |
1 | a0001c0001t0003g0232 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(24): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0219 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(25): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(11): Show |
3 | a0001c0001t0003g0041 a0001c0001t0003g0224 a0001c0001t0003g0235 |
3 | HG00544.hp1 HG02109.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(12): Show |
4 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0238 others(1): Show |
5 | HG00438.hp1 HG03516.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(21): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0007 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATTT others(3): Show |
3 | a0001c0001t0002g0022 a0001c0001t0002g0079 a0001c0001t0002g0081 |
3 | HG01081.hp1 HG01167.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | ATATATTT others(13): Show |
1 | a0001c0001t0003g0002 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.103+1490_103+1491i others(22): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440674 | A | T | 7 | a0001c0002t0001g0003 a0001c0002t0001g0212 a0001c0002t0001g0213 others(4): Show |
8 | HG01109.hp2 HG02165.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.103+1489A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440674 | |||||||
| chr7:99440674 | AT | A | 25 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0017 others(22): Show |
26 | HG00323.hp2 HG00735.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.103+1508delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440674 | ||||||
| chr7:99440675 | T | TA | 22 | a0001c0002t0001g0015 a0001c0002t0001g0119 a0001c0002t0001g0127 others(19): Show |
24 | HG00099.hp2 HG00544.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.103+1490_103+1491i others(3): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440675 | |||||||
| chr7:99440675 | T | TATATATA others(2): Show |
3 | a0001c0001t0002g0044 a0001c0001t0003g0118 a0001c0003t0002g0092 |
3 | HG01081.hp2 HG03453.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.103+1490_103+1491i others(11): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440675 | |||||||
| chr7:99440675 | T | TATATATA others(20): Show |
1 | a0001c0003t0002g0091 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.103+1490_103+1491i others(29): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440675 | |||||||
| chr7:99440676 | T | A | 58 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0003g0026 others(55): Show |
80 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.103+1491T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440676 | |||||||
| chr7:99440676 | T | G | 1 | a0001c0001t0002g0047 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.103+1491T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440676 | |||||||
| chr7:99440677 | T | A | 36 | a0001c0001t0003g0118 a0001c0002t0001g0015 a0001c0002t0001g0028 others(33): Show |
39 | HG00544.hp2 HG00735.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.103+1492T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440677 | |||||||
| chr7:99440678 | T | A | 13 | a0001c0002t0001g0010 a0001c0002t0001g0120 a0001c0002t0001g0121 others(10): Show |
16 | HG00597.hp2 HG01123.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.103+1493T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440678 | |||||||
| chr7:99440679 | T | A | 4 | a0001c0002t0001g0119 a0001c0002t0001g0172 a0001c0002t0001g0173 others(1): Show |
4 | HG01081.hp2 HG01952.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+1494T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440679 | |||||||
| chr7:99440680 | T | A | 1 | a0001c0003t0002g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.103+1495T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440680 | |||||||
| chr7:99440682 | T | G | 3 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0050 |
3 | HG02965.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.103+1497T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440682 | |||||||
| chr7:99440693 | T | C | 1 | a0001c0003t0002g0104 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.103+1508T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440693 | |||||||
| chr7:99440706 | A | ACAACTTT others(18): Show |
1 | a0001c0002t0001g0246 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.103+1522_103+1546d others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440706 | ||||||
| chr7:99440837 | C | T | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.103+1652C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99440837 | |||||||
| chr7:99440947 | C | CT | 17 | a0001c0001t0003g0245 a0001c0001t0004g0249 a0001c0001t0004g0250 others(14): Show |
18 | HG01081.hp2 HG01169.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.103+1782dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440947 | ||||||
| chr7:99440947 | CT | C | 16 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0051 others(13): Show |
20 | HG00639.hp2 HG01069.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.103+1782delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99440947 | ||||||
| chr7:99441051 | A | G | 4 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0167 others(1): Show |
4 | HG00408.hp2 HG01934.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+1866A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441051 | |||||||
| chr7:99441107 | C | A | 1 | a0001c0001t0007g0195 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.103+1922C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441107 | |||||||
| chr7:99441281 | GA | G | 3 | a0001c0003t0002g0092 a0001c0003t0002g0094 a0001c0003t0002g0114 |
3 | HG01081.hp2 HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.103+2097delA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441281 | |||||||
| chr7:99441283 | G | T | 3 | a0001c0003t0002g0092 a0001c0003t0002g0094 a0001c0003t0002g0114 |
3 | HG01081.hp2 HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.103+2098G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441283 | |||||||
| chr7:99441293 | C | T | 2 | a0001c0001t0004g0252 a0001c0001t0004g0253 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.103+2108C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441293 | |||||||
| chr7:99441389 | C | T | 1 | a0001c0002t0001g0164 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.103+2204C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441389 | |||||||
| chr7:99441690 | A | AT | 51 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0013 others(48): Show |
62 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.103+2515dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99441690 | ||||||
| chr7:99441690 | A | G | 1 | a0001c0002t0001g0169 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.103+2505A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441690 | |||||||
| chr7:99441703 | T | C | 1 | a0001c0002t0001g0121 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.103+2518T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441703 | |||||||
| chr7:99441827 | G | A | 29 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(26): Show |
30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.103+2642G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441827 | |||||||
| chr7:99441981 | C | T | 29 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(26): Show |
30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.103+2796C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99441981 | |||||||
| chr7:99442004 | T | C | 29 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(26): Show |
30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.104-2785T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442004 | |||||||
| chr7:99442220 | A | G | 3 | a0001c0003t0002g0091 a0001c0003t0002g0100 a0001c0003t0002g0101 |
3 | HG02970.hp1 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.104-2569A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442220 | |||||||
| chr7:99442411 | C | T | 2 | a0001c0001t0004g0250 a0001c0001t0004g0251 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.104-2378C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442411 | |||||||
| chr7:99442453 | G | A | 1 | a0001c0003t0002g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.104-2336G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442453 | |||||||
| chr7:99442453 | G | C | 1 | a0001c0002t0001g0165 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.104-2336G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442453 | |||||||
| chr7:99442642 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.104-2147C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442642 | |||||||
| chr7:99442650 | C | T | 51 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0007 others(48): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.104-2139C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442650 | |||||||
| chr7:99442651 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.104-2138G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442651 | |||||||
| chr7:99442655 | C | CA | 34 | a0001c0002t0001g0017 a0001c0002t0001g0128 a0001c0002t0001g0129 others(31): Show |
37 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.104-2114dupA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | ||||||
| chr7:99442655 | C | CAA | 30 | a0001c0001t0002g0022 a0001c0001t0002g0044 a0001c0001t0002g0045 others(27): Show |
31 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.104-2115_104-2114d others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | ||||||
| chr7:99442655 | C | CAAA | 31 | a0001c0001t0002g0047 a0001c0001t0002g0075 a0001c0001t0002g0076 others(28): Show |
55 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.104-2116_104-2114d others(5): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | ||||||
| chr7:99442655 | C | CAAAA | 42 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0043 others(39): Show |
60 | HG00639.hp1 HG01070.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.104-2117_104-2114d others(6): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | ||||||
| chr7:99442655 | C | CAAAAA | 11 | a0001c0001t0002g0014 a0001c0001t0002g0048 a0001c0001t0002g0051 others(8): Show |
17 | HG00408.hp1 HG00597.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.104-2118_104-2114d others(7): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442655 | ||||||
| chr7:99442669 | A | AAC | 2 | a0001c0001t0002g0012 a0001c0001t0002g0013 |
6 | HG01884.hp1 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.104-2119_104-2118i others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99442669 | ||||||
| chr7:99442669 | A | AC | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.104-2120_104-2119i others(3): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442669 | |||||||
| chr7:99442669 | A | C | 1 | a0001c0002t0001g0161 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.104-2120A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442669 | |||||||
| chr7:99442676 | C | A | 8 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0007 others(5): Show |
9 | HG01978.hp2 HG02293.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.104-2113C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442676 | |||||||
| chr7:99442749 | C | T | 1 | a0001c0001t0003g0226 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.104-2040C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442749 | |||||||
| chr7:99442837 | G | A | 1 | a0001c0001t0004g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104-1952G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442837 | |||||||
| chr7:99442899 | C | T | 1 | a0001c0001t0007g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.104-1890C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99442899 | |||||||
| chr7:99443343 | T | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.104-1446T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443343 | |||||||
| chr7:99443433 | G | GC | 35 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(32): Show |
36 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.104-1356_104-1355i others(3): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443433 | |||||||
| chr7:99443495 | A | T | 1 | a0001c0001t0003g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.104-1294A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443495 | |||||||
| chr7:99443610 | G | A | 2 | a0001c0003t0002g0106 a0001c0003t0002g0107 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.104-1179G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443610 | |||||||
| chr7:99443748 | A | G | 1 | a0001c0002t0001g0131 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.104-1041A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443748 | |||||||
| chr7:99443788 | G | T | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 |
3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.104-1001G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443788 | |||||||
| chr7:99443793 | C | A | 10 | a0001c0003t0002g0093 a0001c0003t0002g0095 a0001c0003t0002g0096 others(7): Show |
10 | HG00099.hp2 HG01175.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.104-996C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443793 | |||||||
| chr7:99443854 | G | A | 1 | a0001c0002t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.104-935G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443854 | |||||||
| chr7:99443975 | G | C | 30 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(27): Show |
31 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.104-814G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99443975 | |||||||
| chr7:99444297 | A | T | 1 | a0001c0003t0002g0089 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.104-492A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444297 | |||||||
| chr7:99444401 | G | A | 52 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0007 others(49): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.104-388G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444401 | |||||||
| chr7:99444419 | T | C | 24 | a0001c0002t0001g0018 a0001c0002t0001g0024 a0001c0002t0001g0119 others(21): Show |
27 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.104-370T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444419 | |||||||
| chr7:99444457 | C | CA | 7 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(4): Show |
8 | HG00738.hp1 HG02572.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.104-319dupA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 99444457 | ||||||
| chr7:99444487 | G | A | 1 | a0001c0001t0003g0038 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.104-302G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444487 | |||||||
| chr7:99444550 | C | A | 2 | a0001c0002t0001g0189 a0001c0002t0001g0206 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.104-239C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444550 | |||||||
| chr7:99444579 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.104-210C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 1/7 | chr7 | 99444579 | |||||||
| chr7:99444872 | G | A | 1 | a0001c0001t0003g0227 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.154+33G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99444872 | |||||||
| chr7:99444879 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.154+40C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99444879 | |||||||
| chr7:99445022 | C | G | 2 | a0001c0001t0004g0250 a0001c0001t0004g0251 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.154+183C>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445022 | |||||||
| chr7:99445071 | G | A | 12 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0022 others(9): Show |
17 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.154+232G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445071 | |||||||
| chr7:99445241 | C | A | 1 | a0001c0002t0001g0127 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.154+402C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445241 | |||||||
| chr7:99445276 | T | A | 1 | a0001c0001t0003g0228 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.154+437T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445276 | |||||||
| chr7:99445277 | C | A | 1 | a0001c0001t0003g0228 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.154+438C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445277 | |||||||
| chr7:99445298 | G | A | 1 | a0001c0003t0002g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.154+459G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445298 | |||||||
| chr7:99445321 | C | T | 1 | a0001c0001t0003g0192 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.154+482C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445321 | |||||||
| chr7:99445372 | C | T | 1 | a0001c0001t0003g0240 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.154+533C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445372 | |||||||
| chr7:99445412 | C | CA | 12 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(9): Show |
12 | HG00558.hp1 HG01081.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+587dupA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99445412 | ||||||
| chr7:99445544 | C | T | 1 | a0001c0002t0001g0024 | 2 | HG00099.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.154+705C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445544 | |||||||
| chr7:99445756 | C | T | 1 | a0001c0003t0002g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.154+917C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445756 | |||||||
| chr7:99445823 | G | A | 3 | a0001c0002t0002g0115 a0001c0002t0002g0116 a0001c0002t0002g0117 |
3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.154+984G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99445823 | |||||||
| chr7:99446041 | G | A | 1 | a0001c0003t0002g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+1202G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446041 | |||||||
| chr7:99446230 | C | A | 4 | a0001c0002t0001g0127 a0001c0002t0001g0132 a0001c0002t0001g0133 others(1): Show |
4 | NA18983.hp1 NA19058.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+1391C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446230 | |||||||
| chr7:99446347 | A | T | 3 | a0001c0001t0003g0041 a0001c0001t0003g0191 a0001c0001t0003g0225 |
4 | HG00544.hp1 NA18963.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+1508A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446347 | |||||||
| chr7:99446604 | CT | C | 17 | a0001c0001t0002g0047 a0001c0001t0002g0061 a0001c0001t0002g0062 others(14): Show |
17 | HG00323.hp1 HG01074.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.155-1502delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446604 | ||||||
| chr7:99446619 | TA | T | 18 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0026 others(15): Show |
20 | HG00621.hp2 HG02040.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.155-1496delA | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446619 | ||||||
| chr7:99446620 | A | T | 73 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(70): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.155-1501A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446620 | |||||||
| chr7:99446621 | A | T | 1 | a0001c0001t0003g0118 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.155-1500A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446621 | |||||||
| chr7:99446699 | C | CT | 3 | a0001c0003t0002g0087 a0001c0003t0002g0088 a0001c0003t0002g0089 |
3 | HG02615.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.155-1421dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446699 | ||||||
| chr7:99446771 | C | CT | 61 | a0001c0001t0002g0047 a0001c0001t0002g0051 a0001c0001t0002g0055 others(58): Show |
94 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.155-1313dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTT | 36 | a0001c0001t0002g0014 a0001c0001t0002g0021 a0001c0001t0002g0045 others(33): Show |
53 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.155-1314_155-1313d others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTT | 18 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0022 others(15): Show |
24 | HG01081.hp1 HG01167.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.155-1315_155-1313d others(5): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTT | 15 | a0001c0001t0002g0013 a0001c0001t0002g0048 a0001c0001t0002g0050 others(12): Show |
18 | HG00438.hp1 HG01069.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.155-1316_155-1313d others(6): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTT | 6 | a0001c0001t0002g0046 a0001c0001t0002g0060 a0001c0001t0002g0073 others(3): Show |
6 | HG01517.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-1317_155-1313d others(7): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0002g0074 a0001c0001t0007g0195 a0001c0002t0002g0115 others(3): Show |
6 | HG02083.hp1 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-1320_155-1313d others(10): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.155-1322_155-1313d others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTTTT others(4): Show |
2 | a0001c0003t0002g0103 a0001c0003t0002g0248 |
2 | HG00099.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.155-1323_155-1313d others(13): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.155-1324_155-1313d others(14): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0082 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.155-1325_155-1313d others(15): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0010g0083 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.155-1326_155-1313d others(16): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTTTT others(11): Show |
2 | a0001c0003t0002g0087 a0001c0003t0002g0088 |
2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.155-1330_155-1313d others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTTTT others(18): Show |
1 | a0001c0003t0002g0089 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155-1337_155-1313d others(27): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | C | CTTTTTTT others(20): Show |
1 | a0001c0003t0002g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.155-1339_155-1313d others(29): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | CT | C | 16 | a0001c0001t0002g0061 a0001c0001t0003g0002 a0001c0001t0003g0039 others(13): Show |
27 | HG00280.hp2 HG01070.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-1313delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0009g0097 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.155-1325_155-1313d others(15): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | CTTTTTTT others(8): Show |
C | 1 | a0001c0002t0001g0202 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.155-1327_155-1313d others(17): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | CTTTTTTT others(10): Show |
C | 1 | a0001c0002t0001g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.155-1329_155-1313d others(19): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | CTTTTTTT others(11): Show |
C | 2 | a0001c0002t0001g0024 a0001c0002t0001g0146 |
3 | HG00099.hp1 HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.155-1330_155-1313d others(20): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446771 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0002g0077 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.155-1333_155-1313d others(23): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99446771 | ||||||
| chr7:99446774 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.155-1347T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446774 | |||||||
| chr7:99446809 | A | G | 145 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0013 others(142): Show |
200 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.155-1312A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446809 | |||||||
| chr7:99446880 | C | T | 2 | a0001c0002t0001g0029 a0001c0002t0001g0205 |
3 | HG00738.hp1 HG04228.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.155-1241C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99446880 | |||||||
| chr7:99447042 | T | C | 35 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(32): Show |
36 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.155-1079T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447042 | |||||||
| chr7:99447056 | A | G | 35 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(32): Show |
36 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.155-1065A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447056 | |||||||
| chr7:99447109 | G | GCTTA | 145 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0013 others(142): Show |
200 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.155-995_155-992dup others(4): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447109 | ||||||
| chr7:99447255 | CTTTCTTT others(5): Show |
C | 45 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0022 others(42): Show |
51 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.155-850_155-839del others(12): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447255 | ||||||
| chr7:99447259 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.155-850_155-838del others(13): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447259 | ||||||
| chr7:99447263 | T | A | 1 | a0001c0002t0001g0027 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.155-858T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447263 | |||||||
| chr7:99447283 | T | C | 1 | a0001c0002t0001g0135 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.155-838T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447283 | |||||||
| chr7:99447291 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.155-830A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447291 | |||||||
| chr7:99447339 | G | A | 3 | a0001c0002t0001g0031 a0001c0002t0001g0204 a0001c0002t0001g0208 |
4 | HG00423.hp2 HG02074.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-782G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447339 | |||||||
| chr7:99447350 | C | A | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-771C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447350 | |||||||
| chr7:99447541 | C | T | 1 | a0001c0003t0002g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.155-580C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447541 | |||||||
| chr7:99447589 | C | CT | 63 | a0001c0001t0002g0043 a0001c0001t0002g0068 a0001c0001t0002g0072 others(60): Show |
105 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.155-514dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447589 | ||||||
| chr7:99447589 | CT | C | 39 | a0001c0001t0002g0063 a0001c0002t0001g0122 a0001c0002t0001g0128 others(36): Show |
40 | HG00099.hp2 HG00544.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.155-514delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 99447589 | ||||||
| chr7:99447676 | G | A | 11 | a0001c0003t0002g0093 a0001c0003t0002g0095 a0001c0003t0002g0096 others(8): Show |
11 | HG00099.hp2 HG01175.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-445G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447676 | |||||||
| chr7:99447691 | G | C | 1 | a0001c0001t0002g0085 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.155-430G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447691 | |||||||
| chr7:99447794 | A | C | 1 | a0001c0002t0001g0157 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.155-327A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447794 | |||||||
| chr7:99447841 | A | C | 4 | a0001c0003t0002g0092 a0001c0003t0002g0094 a0001c0003t0002g0113 others(1): Show |
4 | HG01081.hp2 HG01891.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-280A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447841 | |||||||
| chr7:99447979 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.155-142G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 2/7 | chr7 | 99447979 | |||||||
| chr7:99448406 | C | T | 1 | a0001c0003t0002g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.307+133C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448406 | |||||||
| chr7:99448459 | C | CT | 13 | a0001c0001t0002g0075 a0001c0001t0002g0078 a0001c0001t0002g0082 others(10): Show |
13 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.307+207dupT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 99448459 | ||||||
| chr7:99448459 | CT | C | 41 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0065 others(38): Show |
44 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.307+207delT | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 99448459 | ||||||
| chr7:99448591 | C | T | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 |
3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.307+318C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448591 | |||||||
| chr7:99448621 | T | C | 3 | a0001c0002t0001g0126 a0001c0002t0001g0181 a0001c0002t0001g0187 |
3 | HG02165.hp1 NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.307+348T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448621 | |||||||
| chr7:99448627 | G | A | 3 | a0001c0002t0001g0126 a0001c0002t0001g0181 a0001c0002t0001g0187 |
3 | HG02165.hp1 NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.307+354G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448627 | |||||||
| chr7:99448643 | A | G | 3 | a0001c0003t0002g0091 a0001c0003t0002g0100 a0001c0003t0002g0101 |
3 | HG02970.hp1 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.307+370A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448643 | |||||||
| chr7:99448849 | A | C | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+576A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448849 | |||||||
| chr7:99448850 | G | T | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+577G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448850 | |||||||
| chr7:99448981 | G | A | 5 | a0001c0001t0002g0053 a0001c0001t0002g0075 a0001c0001t0002g0078 others(2): Show |
5 | HG02559.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+708G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448981 | |||||||
| chr7:99448994 | G | A | 34 | a0001c0001t0002g0009 a0001c0001t0002g0014 a0001c0001t0002g0021 others(31): Show |
40 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.307+721G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99448994 | |||||||
| chr7:99449071 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.307+798G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449071 | |||||||
| chr7:99449078 | A | G | 1 | a0001c0002t0001g0146 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.307+805A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449078 | |||||||
| chr7:99449093 | C | G | 1 | a0001c0001t0002g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.307+820C>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449093 | |||||||
| chr7:99449407 | T | A | 30 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(27): Show |
31 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.308-869T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449407 | |||||||
| chr7:99449476 | G | A | 3 | a0001c0001t0007g0195 a0001c0001t0007g0198 a0001c0001t0007g0201 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.308-800G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449476 | |||||||
| chr7:99449486 | T | G | 2 | a0001c0001t0004g0252 a0001c0001t0004g0253 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.308-790T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449486 | |||||||
| chr7:99449567 | C | T | 4 | a0001c0002t0001g0144 a0001c0002t0001g0145 a0001c0002t0001g0148 others(1): Show |
4 | HG01070.hp2 HG01167.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-709C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449567 | |||||||
| chr7:99449569 | T | C | 1 | a0001c0002t0001g0154 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.308-707T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449569 | |||||||
| chr7:99449749 | T | G | 2 | a0001c0002t0001g0209 a0001c0002t0001g0212 |
2 | NA18942.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.308-527T>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449749 | |||||||
| chr7:99449842 | G | T | 2 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
2 | HG00558.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.308-434G>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449842 | |||||||
| chr7:99449859 | G | C | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 |
3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.308-417G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99449859 | |||||||
| chr7:99450170 | G | A | 1 | a0001c0002t0001g0158 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.308-106G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99450170 | |||||||
| chr7:99450174 | G | A | 1 | a0001c0002t0001g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.308-102G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99450174 | |||||||
| chr7:99450190 | A | G | 3 | a0001c0001t0007g0195 a0001c0001t0007g0198 a0001c0001t0007g0201 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.308-86A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 3/7 | chr7 | 99450190 | |||||||
| chr7:99450398 | G | A | 3 | a0001c0001t0007g0195 a0001c0001t0007g0198 a0001c0001t0007g0201 |
3 | HG01884.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.403+27G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450398 | |||||||
| chr7:99450509 | C | T | 4 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+138C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450509 | |||||||
| chr7:99450520 | C | A | 35 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(32): Show |
36 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.403+149C>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450520 | |||||||
| chr7:99450603 | C | T | 4 | a0001c0003t0002g0092 a0001c0003t0002g0094 a0001c0003t0002g0113 others(1): Show |
4 | HG01081.hp2 HG01891.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-99C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450603 | |||||||
| chr7:99450680 | G | A | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 |
3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.404-22G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 4/7 | chr7 | 99450680 | |||||||
| chr7:99450809 | T | C | 142 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0013 others(139): Show |
197 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.497+14T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99450809 | |||||||
| chr7:99450916 | G | A | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+121G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99450916 | |||||||
| chr7:99450964 | T | C | 1 | a0001c0003t0002g0248 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.497+169T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99450964 | |||||||
| chr7:99451000 | G | A | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 |
3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.497+205G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451000 | |||||||
| chr7:99451038 | A | G | 3 | a0001c0002t0002g0115 a0001c0002t0002g0116 a0001c0002t0002g0117 |
3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497+243A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451038 | |||||||
| chr7:99451475 | C | T | 50 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0013 others(47): Show |
61 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.497+680C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451475 | |||||||
| chr7:99451541 | G | C | 30 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(27): Show |
31 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.497+746G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451541 | |||||||
| chr7:99451566 | C | T | 19 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(16): Show |
20 | HG00099.hp2 HG01175.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.497+771C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451566 | |||||||
| chr7:99451691 | G | A | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 |
3 | HG02647.hp1 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.498-677G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451691 | |||||||
| chr7:99451766 | G | A | 19 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(16): Show |
20 | HG00099.hp2 HG01175.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.498-602G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451766 | |||||||
| chr7:99451780 | A | G | 145 | a0001c0001t0002g0009 a0001c0001t0002g0012 a0001c0001t0002g0013 others(142): Show |
200 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.498-588A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451780 | |||||||
| chr7:99451871 | C | T | 6 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0050 others(3): Show |
6 | HG01243.hp2 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-497C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99451871 | |||||||
| chr7:99452059 | C | T | 12 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0022 others(9): Show |
17 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.498-309C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99452059 | |||||||
| chr7:99452167 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.498-201G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99452167 | |||||||
| chr7:99452190 | G | A | 1 | a0001c0001t0004g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.498-178G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99452190 | |||||||
| chr7:99452253 | C | T | 16 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0022 others(13): Show |
21 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.498-115C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 5/7 | chr7 | 99452253 | |||||||
| chr7:99452489 | C | T | 1 | a0001c0002t0001g0214 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.570+49C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99452489 | |||||||
| chr7:99452509 | A | T | 1 | a0001c0001t0002g0077 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.570+69A>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99452509 | |||||||
| chr7:99452700 | G | A | 54 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0007 others(51): Show |
97 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.570+260G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99452700 | |||||||
| chr7:99452759 | C | T | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+319C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99452759 | |||||||
| chr7:99453323 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.571-643G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99453323 | |||||||
| chr7:99453364 | G | A | 11 | a0001c0003t0002g0093 a0001c0003t0002g0095 a0001c0003t0002g0096 others(8): Show |
11 | HG00099.hp2 HG01175.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.571-602G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99453364 | |||||||
| chr7:99453414 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.571-552C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99453414 | |||||||
| chr7:99453616 | C | T | 1 | a0001c0001t0003g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.571-350C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | chr7 | 99453616 | |||||||
| chr7:99453801 | TCAC | T | 6 | a0001c0003t0002g0091 a0001c0003t0002g0100 a0001c0003t0002g0101 others(3): Show |
6 | HG02258.hp1 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-161_571-159del others(3): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 99453801 | ||||||
| chr7:99454185 | T | A | 1 | a0001c0001t0003g0228 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.741+49T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454185 | |||||||
| chr7:99454233 | A | C | 16 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0022 others(13): Show |
21 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.741+97A>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454233 | |||||||
| chr7:99454306 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.741+170T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454306 | |||||||
| chr7:99454462 | G | A | 4 | a0001c0001t0003g0219 a0001c0002t0002g0115 a0001c0002t0002g0116 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+326G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454462 | |||||||
| chr7:99454805 | T | C | 91 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0199 others(88): Show |
135 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.741+669T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454805 | |||||||
| chr7:99454927 | C | T | 3 | a0001c0002t0002g0115 a0001c0002t0002g0116 a0001c0002t0002g0117 |
3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.741+791C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454927 | |||||||
| chr7:99454951 | A | G | 1 | a0001c0002t0001g0164 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.741+815A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99454951 | |||||||
| chr7:99455048 | CTT | C | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.741+914_741+915del others(2): Show |
CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 99455048 | ||||||
| chr7:99455087 | A | G | 29 | a0001c0003t0002g0023 a0001c0003t0002g0087 a0001c0003t0002g0088 others(26): Show |
30 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.741+951A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455087 | |||||||
| chr7:99455283 | T | A | 1 | a0001c0001t0003g0228 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.741+1147T>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455283 | |||||||
| chr7:99455485 | G | A | 2 | a0001c0002t0001g0140 a0001c0002t0001g0158 |
2 | NA18965.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.742-947G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455485 | |||||||
| chr7:99455552 | T | C | 2 | a0001c0001t0002g0196 a0001c0001t0002g0199 |
2 | HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.742-880T>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455552 | |||||||
| chr7:99455585 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.742-847C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455585 | |||||||
| chr7:99455678 | G | A | 1 | a0001c0002t0001g0156 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.742-754G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455678 | |||||||
| chr7:99455691 | G | C | 34 | a0001c0001t0002g0009 a0001c0001t0002g0014 a0001c0001t0002g0021 others(31): Show |
40 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.742-741G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455691 | |||||||
| chr7:99455754 | G | A | 16 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0022 others(13): Show |
21 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.742-678G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455754 | |||||||
| chr7:99455789 | C | T | 1 | a0001c0002t0008g0176 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.742-643C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455789 | |||||||
| chr7:99455841 | C | G | 1 | a0001c0002t0001g0136 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.742-591C>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455841 | |||||||
| chr7:99455876 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.742-556C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455876 | |||||||
| chr7:99455948 | A | G | 1 | a0001c0003t0002g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.742-484A>G | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99455948 | |||||||
| chr7:99456048 | C | T | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-384C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456048 | |||||||
| chr7:99456176 | C | T | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-256C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456176 | |||||||
| chr7:99456186 | C | T | 2 | a0001c0003t0002g0111 a0001c0003t0002g0112 |
2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.742-246C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456186 | |||||||
| chr7:99456193 | G | A | 13 | a0001c0001t0002g0014 a0001c0001t0002g0021 a0001c0001t0002g0047 others(10): Show |
16 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.742-239G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456193 | |||||||
| chr7:99456203 | G | C | 1 | a0001c0002t0001g0183 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.742-229G>C | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456203 | |||||||
| chr7:99456210 | C | T | 1 | a0001c0001t0003g0220 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.742-222C>T | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456210 | |||||||
| chr7:99456211 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.742-221G>A | CPSF4 | ENSG00000160917.15 | transcript | ENST00000292476.10 | protein_coding | 7/7 | chr7 | 99456211 |