Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79869 |
| ensemblid | ENSG00000149532.16 |
| hgncid | 30098 |
| symbol | CPSF7 |
| name | cleavage and polyadenylation specific factor 7 |
| refseq_nuc | NM_001142565.3 |
| refseq_prot | NP_001136037.1 |
| ensembl_nuc | ENST00000439958.8 |
| ensembl_prot | ENSP00000397203.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 61402729 |
| end | 61429975 |
| strand | - |
| ver | v1.2 |
| region | chr11:61402729-61429975 |
| region5000 | chr11:61397729-61434975 |
| regionname0 | CPSF7_chr11_61402729_61429975 |
| regionname5000 | CPSF7_chr11_61397729_61434975 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1386 | 97 | 71 | 11 | 5 | 2 | 7 | CPSF7_chr11_61397729_61434975 | CPSF7 | ATGTC others(1381): Show |
chr11 | 61397729 | 61434975 | ||
| a0001c0002 | 0/1 | 1386 | 93 | 17 | 29 | 23 | 4 | 19 | CPSF7_chr11_61397729_61434975 | CPSF7 | ATGTC others(1381): Show |
chr11 | 61397729 | 61434975 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3487 | 65 | 41 | 9 | 5 | 2 | 7 | CPSF7_chr11_61397729_61434975 | CPSF7 | GGAGA others(3482): Show |
chr11 | 61397729 | 61434975 |
| a0001c0001t0002 | 0/0 | 3486 | 18 | 16 | 2 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | GGAGA others(3481): Show |
chr11 | 61397729 | 61434975 |
| a0001c0001t0003 | 0/0 | 3485 | 9 | 9 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | GGAGA others(3480): Show |
chr11 | 61397729 | 61434975 |
| a0001c0001t0004 | 0/0 | 3487 | 5 | 5 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | GGAGA others(3482): Show |
chr11 | 61397729 | 61434975 |
| a0001c0002t0001 | 0/1 | 3487 | 87 | 17 | 29 | 17 | 4 | 19 | CPSF7_chr11_61397729_61434975 | CPSF7 | GGAGA others(3482): Show |
chr11 | 61397729 | 61434975 |
| a0001c0002t0005 | 0/0 | 3487 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | GGAGA others(3482): Show |
chr11 | 61397729 | 61434975 |
| a0001c0002t0006 | 0/0 | 3487 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | GGAGA others(3482): Show |
chr11 | 61397729 | 61434975 |
| a0001c0002t0007 | 0/0 | 3487 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | GGAGA others(3482): Show |
chr11 | 61397729 | 61434975 |
| a0001c0002t0008 | 0/0 | 3487 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | GGAGA others(3482): Show |
chr11 | 61397729 | 61434975 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0003g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0001 | 0/0 | 11 | 2 | 3 | 2 | 1 | 3 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0002 | 0/0 | 7 | 2 | 1 | 1 | 1 | 2 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| a0001c0002t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0058 | EUR | GBR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00673 | hp1 | a0001 | c0002 | t0007 | g0018 | EAS | CHS | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00673 | hp2 | a0001 | c0002 | t0008 | g0103 | EAS | CHS | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0057 | EUR | IBS | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02083 | hp2 | a0001 | c0002 | t0006 | g0082 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02129 | hp2 | a0001 | c0002 | t0005 | g0073 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | CDX | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0062 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | STU | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | STU | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | STU | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19001 | hp1 | a0001 | c0002 | t0006 | g0107 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19075 | hp2 | a0001 | c0002 | t0005 | g0093 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ASW | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ASW | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | GIH | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | GIH | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | USA | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0145 | REF | REF | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0033 | REF | REF | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61411813 | G | A | 1 | a0001c0002 | 92 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(89): Show |
synonymous_variant | LOW | c.1182C>T | p.Ile394Ile | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/10 | 1299/3487 | 1182/1389 | 394/462 | chr11 | 61411813 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61402920 | G | A | 1 | a0001c0002t0005 | 2 | HG02129.hp2 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1790C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 8023 | chr11 | 61402920 | ||||||
| chr11:61402969 | AC | A | 2 | a0001c0001t0002 a0001c0001t0003 |
27 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1740delG | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 7973 | chr11 | 61402969 | ||||||
| chr11:61404398 | C | T | 1 | a0001c0002t0008 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*312G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 6545 | chr11 | 61404398 | ||||||
| chr11:61404444 | G | A | 1 | a0001c0002t0006 | 2 | HG02083.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*266C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 6499 | chr11 | 61404444 | ||||||
| chr11:61404467 | AC | A | 1 | a0001c0001t0003 | 9 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*242delG | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 6475 | chr11 | 61404467 | ||||||
| chr11:61404594 | G | C | 1 | a0001c0001t0004 | 5 | HG02451.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*116C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 6349 | chr11 | 61404594 | ||||||
| chr11:61429947 | C | G | 1 | a0001c0002t0007 | 1 | HG00673.hp1 | 5_prime_UTR_variant | MODIFIER | c.-89G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/10 | 712 | chr11 | 61429947 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61404851 | CAA | C | 1 | a0001c0001t0003g0015 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.*6-149_*6-148delTT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61404851 | |||||||
| chr11:61404860 | A | C | 1 | a0001c0002t0001g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.*6-156T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61404860 | |||||||
| chr11:61405024 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.*6-320T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405024 | |||||||
| chr11:61405169 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.*6-465G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405169 | |||||||
| chr11:61405235 | CAT | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.*6-533_*6-532delAT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405235 | |||||||
| chr11:61405333 | A | G | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.*6-629T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405333 | |||||||
| chr11:61405365 | T | C | 5 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.*6-661A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405365 | |||||||
| chr11:61405402 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.*6-698G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405402 | |||||||
| chr11:61405864 | C | T | 110 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(107): Show |
145 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(142): Show |
intron_variant | MODIFIER | c.*6-1160G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405864 | |||||||
| chr11:61406013 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.*6-1309G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406013 | |||||||
| chr11:61406142 | T | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
187 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(184): Show |
intron_variant | MODIFIER | c.*6-1438A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406142 | |||||||
| chr11:61406143 | A | G | 1 | a0001c0002t0001g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*6-1439T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406143 | |||||||
| chr11:61406318 | G | C | 2 | a0001c0002t0001g0074 a0001c0002t0001g0108 |
2 | HG01943.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.*6-1614C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406318 | |||||||
| chr11:61406403 | C | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0041 others(1): Show |
5 | HG01081.hp1 HG01978.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.*6-1699G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406403 | |||||||
| chr11:61406667 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*6-1963T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406667 | |||||||
| chr11:61406787 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*6-2083C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406787 | |||||||
| chr11:61406887 | C | CT | 3 | a0001c0001t0002g0007 a0001c0001t0002g0125 a0001c0001t0002g0126 |
5 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.*6-2184dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406887 | |||||||
| chr11:61406958 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*6-2254C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406958 | |||||||
| chr11:61407444 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*6-2740G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61407444 | |||||||
| chr11:61408057 | C | CT | 28 | a0001c0001t0001g0017 a0001c0001t0001g0110 a0001c0001t0001g0111 others(25): Show |
35 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.*5+2880dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408057 | |||||||
| chr11:61408057 | C | CTT | 13 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0115 others(10): Show |
15 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.*5+2879_*5+2880dup others(2): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408057 | |||||||
| chr11:61408149 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.*5+2789G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408149 | |||||||
| chr11:61408183 | A | T | 1 | a0001c0001t0004g0048 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*5+2755T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408183 | |||||||
| chr11:61408229 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0003g0113 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*5+2709A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408229 | |||||||
| chr11:61408353 | C | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0047 |
3 | HG01109.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.*5+2585G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408353 | |||||||
| chr11:61408532 | G | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.*5+2406C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408532 | |||||||
| chr11:61408637 | A | C | 20 | a0001c0001t0001g0115 a0001c0001t0002g0005 a0001c0001t0002g0007 others(17): Show |
28 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.*5+2301T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408637 | |||||||
| chr11:61408901 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.*5+2037G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408901 | |||||||
| chr11:61408952 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0123 others(2): Show |
7 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.*5+1986C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408952 | |||||||
| chr11:61409107 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.*5+1831A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409107 | |||||||
| chr11:61409148 | T | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG02080.hp1 NA18950.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.*5+1790A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409148 | |||||||
| chr11:61409167 | A | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
52 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(49): Show |
intron_variant | MODIFIER | c.*5+1771T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409167 | |||||||
| chr11:61409194 | C | A | 1 | a0001c0002t0001g0074 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.*5+1744G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409194 | |||||||
| chr11:61409286 | A | T | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG01255.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.*5+1652T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409286 | |||||||
| chr11:61409328 | C | T | 11 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0120 others(8): Show |
16 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.*5+1610G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409328 | |||||||
| chr11:61409333 | G | A | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(65): Show |
92 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.*5+1605C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409333 | |||||||
| chr11:61409664 | GT | G | 107 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(104): Show |
142 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.*5+1273delA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409664 | |||||||
| chr11:61409948 | C | T | 7 | a0001c0001t0002g0005 a0001c0001t0002g0120 a0001c0001t0002g0121 others(4): Show |
10 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.*5+990G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409948 | |||||||
| chr11:61409987 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.*5+951C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409987 | |||||||
| chr11:61410479 | AATG | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0110 others(9): Show |
14 | HG01243.hp2 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.*5+456_*5+458delCA others(1): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61410479 | |||||||
| chr11:61410554 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0039 |
2 | HG01433.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.*5+384A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61410554 | |||||||
| chr11:61411340 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227-235C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/9 | chr11 | 61411340 | |||||||
| chr11:61411534 | T | C | 110 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(107): Show |
145 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(142): Show |
intron_variant | MODIFIER | c.1226+235A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/9 | chr11 | 61411534 | |||||||
| chr11:61411537 | G | C | 1 | a0001c0002t0001g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1226+232C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/9 | chr11 | 61411537 | |||||||
| chr11:61411555 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1226+214T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/9 | chr11 | 61411555 | |||||||
| chr11:61412256 | G | A | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(65): Show |
92 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.1058-319C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412256 | |||||||
| chr11:61412359 | G | A | 6 | a0001c0001t0002g0007 a0001c0001t0002g0125 a0001c0001t0002g0126 others(3): Show |
8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1058-422C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412359 | |||||||
| chr11:61412390 | C | T | 2 | a0001c0002t0006g0082 a0001c0002t0006g0107 |
2 | HG02083.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1058-453G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412390 | |||||||
| chr11:61412506 | G | C | 1 | a0001c0002t0001g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1058-569C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412506 | |||||||
| chr11:61412604 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1058-667T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412604 | |||||||
| chr11:61412705 | G | A | 1 | a0001c0002t0001g0089 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1058-768C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412705 | |||||||
| chr11:61412779 | G | A | 1 | a0001c0002t0001g0076 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1058-842C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412779 | |||||||
| chr11:61412887 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1058-950A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412887 | |||||||
| chr11:61412911 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1058-974A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412911 | |||||||
| chr11:61413007 | A | T | 42 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(39): Show |
53 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(50): Show |
intron_variant | MODIFIER | c.1058-1070T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413007 | |||||||
| chr11:61413317 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1058-1380T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413317 | |||||||
| chr11:61413440 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1058-1503C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413440 | |||||||
| chr11:61413505 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1058-1568G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413505 | |||||||
| chr11:61413633 | C | CA | 8 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
10 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1058-1697dupT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413633 | |||||||
| chr11:61413633 | CAA | C | 5 | a0001c0001t0003g0006 a0001c0001t0003g0015 a0001c0001t0003g0114 others(2): Show |
8 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1058-1698_1058-169 others(6): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413633 | |||||||
| chr11:61413747 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1058-1810G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413747 | |||||||
| chr11:61413820 | A | G | 3 | a0001c0001t0002g0007 a0001c0001t0002g0125 a0001c0001t0002g0126 |
5 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057+1846T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413820 | |||||||
| chr11:61414109 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1057+1557T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414109 | |||||||
| chr11:61414148 | A | AT | 109 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(106): Show |
139 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.1057+1517dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414148 | |||||||
| chr11:61414148 | A | ATT | 12 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0029 others(9): Show |
13 | HG01081.hp1 HG01257.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1057+1516_1057+151 others(6): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414148 | |||||||
| chr11:61414148 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0014 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1057+1508_1057+151 others(14): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414148 | |||||||
| chr11:61414313 | T | C | 2 | a0001c0001t0002g0132 a0001c0001t0002g0136 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1057+1353A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414313 | |||||||
| chr11:61414625 | A | T | 1 | a0001c0002t0001g0011 | 2 | HG01978.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1057+1041T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414625 | |||||||
| chr11:61414851 | C | T | 1 | a0001c0002t0001g0083 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1057+815G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414851 | |||||||
| chr11:61414862 | C | A | 1 | a0001c0002t0001g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1057+804G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414862 | |||||||
| chr11:61415073 | CA | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057+592delT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61415073 | |||||||
| chr11:61415161 | C | A | 1 | a0001c0002t0001g0062 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1057+505G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61415161 | |||||||
| chr11:61415199 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1057+467G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61415199 | |||||||
| chr11:61415594 | A | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0029 |
2 | NA18950.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1057+72T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61415594 | |||||||
| chr11:61415857 | T | C | 2 | a0001c0002t0001g0078 a0001c0002t0001g0083 |
2 | HG01928.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.939-73A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415857 | |||||||
| chr11:61415867 | A | G | 1 | a0001c0001t0003g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.939-83T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415867 | |||||||
| chr11:61415898 | A | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
10 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.939-114T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415898 | |||||||
| chr11:61415902 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.939-118T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415902 | |||||||
| chr11:61415916 | C | T | 9 | a0001c0002t0001g0057 a0001c0002t0001g0068 a0001c0002t0001g0081 others(6): Show |
9 | HG01123.hp1 HG01261.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.939-132G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415916 | |||||||
| chr11:61416082 | C | G | 3 | a0001c0002t0001g0066 a0001c0002t0001g0067 a0001c0002t0001g0148 |
3 | HG01255.hp1 HG01433.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.938+23G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61416082 | |||||||
| chr11:61416557 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.524-38A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416557 | |||||||
| chr11:61416569 | C | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0110 others(9): Show |
14 | HG01243.hp2 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-50G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416569 | |||||||
| chr11:61416639 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-120C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416639 | |||||||
| chr11:61416739 | GAATGTTT others(9): Show |
G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0110 others(9): Show |
14 | HG01243.hp2 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-236_524-221del others(16): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416739 | |||||||
| chr11:61416755 | T | G | 30 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0130 others(27): Show |
39 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(36): Show |
intron_variant | MODIFIER | c.524-236A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416755 | |||||||
| chr11:61417116 | A | G | 1 | a0001c0002t0001g0011 | 2 | HG01978.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.524-597T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417116 | |||||||
| chr11:61417178 | T | C | 5 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0050 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-659A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417178 | |||||||
| chr11:61417315 | A | G | 1 | a0001c0001t0003g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.524-796T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417315 | |||||||
| chr11:61417401 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.524-882C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417401 | |||||||
| chr11:61417529 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.524-1010C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417529 | |||||||
| chr11:61417685 | T | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
52 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(49): Show |
intron_variant | MODIFIER | c.524-1166A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417685 | |||||||
| chr11:61417732 | G | C | 60 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0010 others(57): Show |
80 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.524-1213C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417732 | |||||||
| chr11:61417746 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.524-1227C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417746 | |||||||
| chr11:61418055 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.524-1536T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418055 | |||||||
| chr11:61418231 | C | A | 41 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
52 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(49): Show |
intron_variant | MODIFIER | c.524-1712G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418231 | |||||||
| chr11:61418249 | G | C | 1 | a0001c0002t0001g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.523+1700C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418249 | |||||||
| chr11:61418366 | T | C | 3 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0136 |
3 | HG02622.hp1 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.523+1583A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418366 | |||||||
| chr11:61418563 | C | T | 1 | a0001c0002t0001g0055 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.523+1386G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418563 | |||||||
| chr11:61418724 | C | CT | 3 | a0001c0001t0002g0007 a0001c0001t0002g0125 a0001c0001t0002g0126 |
5 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+1224dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418724 | |||||||
| chr11:61418724 | CT | C | 7 | a0001c0002t0001g0003 a0001c0002t0001g0020 a0001c0002t0001g0084 others(4): Show |
11 | HG01168.hp2 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.523+1224delA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418724 | |||||||
| chr11:61418764 | G | A | 1 | a0001c0002t0001g0019 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.523+1185C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418764 | |||||||
| chr11:61418782 | A | C | 1 | a0001c0002t0001g0098 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.523+1167T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418782 | |||||||
| chr11:61419143 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.523+806G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419143 | |||||||
| chr11:61419197 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.523+752A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419197 | |||||||
| chr11:61419349 | A | C | 42 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(39): Show |
53 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(50): Show |
intron_variant | MODIFIER | c.523+600T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419349 | |||||||
| chr11:61419510 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.523+439A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419510 | |||||||
| chr11:61419896 | C | G | 1 | a0001c0002t0001g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.523+53G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419896 | |||||||
| chr11:61419897 | C | G | 4 | a0001c0001t0003g0006 a0001c0001t0003g0015 a0001c0001t0003g0116 others(1): Show |
7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.523+52G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419897 | |||||||
| chr11:61419899 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.523+50A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419899 | |||||||
| chr11:61420710 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.274-137G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 3/9 | chr11 | 61420710 | |||||||
| chr11:61420795 | A | C | 1 | a0001c0001t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.274-222T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 3/9 | chr11 | 61420795 | |||||||
| chr11:61420962 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.274-389G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 3/9 | chr11 | 61420962 | |||||||
| chr11:61421642 | C | G | 1 | a0001c0001t0002g0125 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.55-34G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421642 | |||||||
| chr11:61421665 | T | C | 20 | a0001c0001t0001g0115 a0001c0001t0002g0005 a0001c0001t0002g0007 others(17): Show |
28 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.55-57A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421665 | |||||||
| chr11:61421683 | G | C | 1 | a0001c0002t0001g0097 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.55-75C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421683 | |||||||
| chr11:61421712 | T | G | 13 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0120 others(10): Show |
18 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.55-104A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421712 | |||||||
| chr11:61421816 | CTGTTAAT others(21): Show |
C | 1 | a0001c0001t0001g0008 | 2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.55-236_55-209delAA others(26): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421816 | |||||||
| chr11:61421834 | G | C | 29 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0130 others(26): Show |
38 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.55-226C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421834 | |||||||
| chr11:61421846 | A | T | 1 | a0001c0001t0001g0008 | 2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.55-238T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421846 | |||||||
| chr11:61421977 | C | T | 6 | a0001c0002t0001g0057 a0001c0002t0001g0098 a0001c0002t0001g0099 others(3): Show |
6 | HG01123.hp1 HG01261.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-369G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421977 | |||||||
| chr11:61422042 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.55-434T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422042 | |||||||
| chr11:61422139 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.55-531A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422139 | |||||||
| chr11:61422198 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.55-590C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422198 | |||||||
| chr11:61422278 | T | C | 1 | a0001c0002t0001g0079 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.55-670A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422278 | |||||||
| chr11:61422471 | T | C | 3 | a0001c0002t0001g0060 a0001c0002t0001g0088 a0001c0002t0001g0089 |
3 | NA18988.hp1 NA19075.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.55-863A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422471 | |||||||
| chr11:61422507 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.55-899C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422507 | |||||||
| chr11:61422870 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55-1262G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422870 | |||||||
| chr11:61422903 | T | C | 139 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(136): Show |
175 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(172): Show |
intron_variant | MODIFIER | c.55-1295A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422903 | |||||||
| chr11:61422987 | G | A | 4 | a0001c0001t0003g0006 a0001c0001t0003g0015 a0001c0001t0003g0116 others(1): Show |
7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-1379C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422987 | |||||||
| chr11:61423026 | G | A | 7 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(4): Show |
7 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-1418C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423026 | |||||||
| chr11:61423105 | C | CA | 68 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0029 others(65): Show |
86 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.55-1498dupT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423105 | |||||||
| chr11:61423105 | C | CAA | 32 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0147 others(29): Show |
47 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.55-1499_55-1498dup others(2): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423105 | |||||||
| chr11:61423105 | C | CAAA | 10 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0002t0001g0060 others(7): Show |
10 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-1500_55-1498dup others(3): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423105 | |||||||
| chr11:61423105 | CA | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
8 | HG02451.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-1498delT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423105 | |||||||
| chr11:61423132 | G | T | 110 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(107): Show |
145 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-1524C>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423132 | |||||||
| chr11:61423169 | CT | C | 82 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(79): Show |
107 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.55-1562delA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423169 | |||||||
| chr11:61423169 | CTTT | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
52 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(49): Show |
intron_variant | MODIFIER | c.55-1564_55-1562del others(3): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423169 | |||||||
| chr11:61423325 | A | C | 1 | a0001c0002t0001g0064 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.55-1717T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423325 | |||||||
| chr11:61423417 | C | T | 13 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0120 others(10): Show |
18 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.55-1809G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423417 | |||||||
| chr11:61423568 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.55-1960C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423568 | |||||||
| chr11:61423692 | G | GT | 4 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
5 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-2085dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423692 | |||||||
| chr11:61423746 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 |
3 | HG02451.hp2 HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.55-2138A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423746 | |||||||
| chr11:61423861 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.55-2253A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423861 | |||||||
| chr11:61423875 | A | C | 1 | a0001c0002t0001g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.55-2267T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423875 | |||||||
| chr11:61424037 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.55-2429A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424037 | |||||||
| chr11:61424241 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55-2633C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424241 | |||||||
| chr11:61424285 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.55-2677A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424285 | |||||||
| chr11:61424320 | T | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-2712A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424320 | |||||||
| chr11:61424514 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.55-2906C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424514 | |||||||
| chr11:61424755 | C | CT | 14 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
15 | HG01081.hp1 HG01978.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.55-3148dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424755 | |||||||
| chr11:61424882 | G | C | 20 | a0001c0001t0001g0115 a0001c0001t0002g0005 a0001c0001t0002g0007 others(17): Show |
28 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.55-3274C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424882 | |||||||
| chr11:61424965 | G | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-3357C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424965 | |||||||
| chr11:61425144 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.55-3536C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425144 | |||||||
| chr11:61425326 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.55-3718C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425326 | |||||||
| chr11:61425361 | A | AT | 2 | a0001c0002t0001g0106 a0001c0002t0006g0107 |
2 | NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.55-3754dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425361 | |||||||
| chr11:61425423 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+3759G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425423 | |||||||
| chr11:61425586 | G | T | 1 | a0001c0002t0001g0062 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.54+3596C>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425586 | |||||||
| chr11:61425662 | A | G | 1 | a0001c0002t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.54+3520T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425662 | |||||||
| chr11:61425783 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.54+3399A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425783 | |||||||
| chr11:61426060 | C | T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
10 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+3122G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426060 | |||||||
| chr11:61426411 | G | A | 2 | a0001c0002t0001g0001 a0001c0002t0001g0071 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.54+2771C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426411 | |||||||
| chr11:61426580 | A | C | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.54+2602T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426580 | |||||||
| chr11:61426820 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.54+2362C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426820 | |||||||
| chr11:61426896 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.54+2286G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426896 | |||||||
| chr11:61426936 | G | A | 5 | a0001c0001t0001g0115 a0001c0001t0003g0006 a0001c0001t0003g0015 others(2): Show |
8 | HG02630.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+2246C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426936 | |||||||
| chr11:61427026 | C | CA | 12 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0041 others(9): Show |
13 | HG01081.hp1 HG01978.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+2155dupT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | |||||||
| chr11:61427026 | C | CAA | 8 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0123 others(5): Show |
11 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+2154_54+2155dup others(2): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | |||||||
| chr11:61427026 | C | CAAA | 6 | a0001c0001t0001g0017 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
7 | HG02572.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+2153_54+2155dup others(3): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | |||||||
| chr11:61427026 | C | CAAAA | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0139 others(3): Show |
6 | HG01109.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+2152_54+2155dup others(4): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | |||||||
| chr11:61427026 | C | CAAAAA | 6 | a0001c0001t0001g0134 a0001c0001t0002g0005 a0001c0001t0002g0135 others(3): Show |
9 | HG01496.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+2151_54+2155dup others(5): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | |||||||
| chr11:61427026 | CAAAAA | C | 5 | a0001c0001t0001g0115 a0001c0001t0003g0006 a0001c0001t0003g0015 others(2): Show |
8 | HG02630.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+2151_54+2155del others(5): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | |||||||
| chr11:61427026 | CAAAAAAA others(2): Show |
C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
6 | HG01243.hp2 HG01261.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+2147_54+2155del others(9): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | |||||||
| chr11:61427052 | A | AAG | 13 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0059 others(10): Show |
15 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.54+2129_54+2130ins others(2): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427052 | |||||||
| chr11:61427052 | A | AG | 53 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(50): Show |
75 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.54+2129dupC | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427052 | |||||||
| chr11:61427052 | A | G | 1 | a0001c0002t0001g0060 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.54+2130T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427052 | |||||||
| chr11:61427074 | T | C | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(65): Show |
92 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.54+2108A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427074 | |||||||
| chr11:61427138 | C | A | 6 | a0001c0002t0001g0057 a0001c0002t0001g0098 a0001c0002t0001g0099 others(3): Show |
6 | HG01123.hp1 HG01261.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+2044G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427138 | |||||||
| chr11:61427140 | T | C | 1 | a0001c0002t0008g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.54+2042A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427140 | |||||||
| chr11:61427274 | G | A | 1 | a0001c0002t0001g0104 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.54+1908C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427274 | |||||||
| chr11:61427348 | G | C | 5 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0050 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1834C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427348 | |||||||
| chr11:61427458 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0110 |
2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.54+1724T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427458 | |||||||
| chr11:61427464 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.54+1718G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427464 | |||||||
| chr11:61427519 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.54+1663C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427519 | |||||||
| chr11:61427567 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.54+1615G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427567 | |||||||
| chr11:61427607 | C | G | 2 | a0001c0002t0001g0058 a0001c0002t0001g0059 |
2 | HG00099.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.54+1575G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427607 | |||||||
| chr11:61427655 | G | GA | 5 | a0001c0001t0003g0015 a0001c0002t0001g0013 a0001c0002t0001g0060 others(2): Show |
5 | HG01081.hp2 HG03098.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1526dupT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427655 | |||||||
| chr11:61427764 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.54+1418T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427764 | |||||||
| chr11:61427978 | A | G | 1 | a0001c0002t0001g0057 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.54+1204T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427978 | |||||||
| chr11:61428009 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54+1173A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428009 | |||||||
| chr11:61428093 | C | A | 2 | a0001c0002t0001g0106 a0001c0002t0006g0107 |
2 | NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.54+1089G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428093 | |||||||
| chr11:61428094 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.54+1088C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428094 | |||||||
| chr11:61428118 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.54+1064A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428118 | |||||||
| chr11:61428160 | G | T | 2 | a0001c0002t0001g0055 a0001c0002t0001g0056 |
2 | HG02083.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.54+1022C>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428160 | |||||||
| chr11:61428501 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.54+681A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428501 | |||||||
| chr11:61428571 | T | A | 1 | a0001c0002t0001g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.54+611A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428571 | |||||||
| chr11:61428817 | G | A | 68 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(65): Show |
92 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.54+365C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428817 | |||||||
| chr11:61428822 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.54+360G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428822 | |||||||
| chr11:61429116 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.54+66G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61429116 | |||||||
| chr11:61429131 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54+51A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61429131 | |||||||
| chr11:61429310 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-55-20C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429310 | |||||||
| chr11:61429441 | G | A | 44 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(41): Show |
55 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(52): Show |
intron_variant | MODIFIER | c.-55-151C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429441 | |||||||
| chr11:61429505 | AGCGCCGC others(4): Show |
A | 1 | a0001c0002t0001g0146 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-55-226_-55-216del others(11): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429505 | |||||||
| chr11:61429516 | T | G | 112 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(109): Show |
147 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(144): Show |
intron_variant | MODIFIER | c.-55-226A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429516 | |||||||
| chr11:61429525 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-55-235C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429525 | |||||||
| chr11:61429682 | T | A | 1 | a0001c0002t0001g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-56+232A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429682 | |||||||
| chr11:61429795 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56+119C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429795 | |||||||
| chr11:61429856 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-56+58C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429856 |