Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 53981 |
| ensemblid | ENSG00000165934.13 |
| hgncid | 2325 |
| symbol | CPSF2 |
| name | cleavage and polyadenylation specific factor 2 |
| refseq_nuc | NM_017437.3 |
| refseq_prot | NP_059133.1 |
| ensembl_nuc | ENST00000298875.9 |
| ensembl_prot | ENSP00000298875.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 92121969 |
| end | 92172145 |
| strand | + |
| ver | v1.2 |
| region | chr14:92121969-92172145 |
| region5000 | chr14:92116969-92177145 |
| regionname0 | CPSF2_chr14_92121969_92172145 |
| regionname5000 | CPSF2_chr14_92116969_92177145 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 782 | 387 | 86 | 60 | 183 | 12 | 44 | 145 | CPSF2_chr14_92116969_92177145 | CPSF2 | MTSII others(777): Show |
chr14 | 92116969 | 92177145 |
| a0002 | 0/0 | 782 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | MTSII others(777): Show |
chr14 | 92116969 | 92177145 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2346 | 386 | 86 | 60 | 182 | 12 | 44 | CPSF2_chr14_92116969_92177145 | CPSF2 | ATGAC others(2341): Show |
chr14 | 92116969 | 92177145 | ||
| a0001c0003 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | ATGAC others(2341): Show |
chr14 | 92116969 | 92177145 | ||
| a0002c0002 | 0/0 | 2346 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | ATGAC others(2341): Show |
chr14 | 92116969 | 92177145 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 13002 | 31 | 3 | 1 | 25 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12997): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0002 | 1/0 | 13003 | 26 | 6 | 10 | 0 | 3 | 6 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0003 | 0/0 | 13027 | 22 | 1 | 5 | 14 | 1 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13022): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0004 | 0/0 | 13026 | 18 | 2 | 1 | 14 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0005 | 0/0 | 13021 | 16 | 2 | 2 | 10 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13016): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0006 | 0/0 | 13022 | 11 | 3 | 1 | 7 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13017): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0007 | 0/0 | 13004 | 9 | 0 | 9 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0008 | 0/0 | 13003 | 8 | 2 | 0 | 5 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0009 | 0/0 | 13003 | 8 | 0 | 0 | 7 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0010 | 0/0 | 13028 | 7 | 0 | 3 | 3 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13023): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0011 | 0/0 | 13002 | 5 | 2 | 1 | 0 | 2 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12997): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0012 | 0/0 | 13020 | 5 | 0 | 0 | 5 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13015): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0013 | 0/0 | 13023 | 5 | 0 | 1 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13018): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0014 | 0/0 | 13010 | 4 | 3 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13005): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0015 | 0/0 | 13002 | 4 | 2 | 0 | 0 | 0 | 2 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12997): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0016 | 0/0 | 13019 | 4 | 2 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13014): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0017 | 0/0 | 13020 | 4 | 2 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13015): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0018 | 0/0 | 13028 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13023): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0019 | 0/0 | 13029 | 4 | 0 | 1 | 2 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13024): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0020 | 0/0 | 13009 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13004): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0021 | 0/0 | 13010 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13005): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0022 | 0/0 | 12998 | 3 | 1 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12993): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0023 | 0/0 | 13002 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12997): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0024 | 0/0 | 13003 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0025 | 0/0 | 13005 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13000): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0026 | 0/0 | 13003 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0027 | 0/0 | 13003 | 3 | 1 | 1 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0028 | 0/0 | 13004 | 3 | 1 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0029 | 0/0 | 13026 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0030 | 0/0 | 13003 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0031 | 0/0 | 13008 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13003): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0032 | 0/0 | 13008 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13003): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0033 | 0/0 | 13010 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13005): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0034 | 0/0 | 13031 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13026): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0035 | 0/0 | 13032 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13027): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0036 | 0/0 | 13037 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13032): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0037 | 0/0 | 13033 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13028): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0038 | 0/0 | 13003 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0039 | 0/0 | 13003 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0040 | 0/0 | 12998 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12993): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0041 | 0/0 | 13003 | 2 | 0 | 0 | 0 | 1 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0042 | 0/0 | 13024 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13019): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0043 | 0/0 | 13019 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13014): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0044 | 0/0 | 13022 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13017): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0045 | 0/0 | 13019 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13014): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0046 | 0/0 | 13012 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13007): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0047 | 0/0 | 13027 | 2 | 0 | 0 | 1 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13022): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0048 | 0/0 | 13026 | 2 | 1 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0049 | 0/0 | 13028 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13023): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0050 | 0/0 | 13031 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13026): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0051 | 0/0 | 13023 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13018): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0052 | 0/0 | 12998 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12993): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0053 | 0/0 | 13020 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13015): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0054 | 0/0 | 13021 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13016): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0055 | 0/0 | 13004 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0056 | 0/0 | 13035 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13030): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0057 | 0/0 | 13007 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13002): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0058 | 0/0 | 13008 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13003): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0059 | 0/0 | 13008 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13003): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0060 | 0/0 | 13030 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13025): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0061 | 0/0 | 13030 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13025): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0062 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13027): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0063 | 0/0 | 13031 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13026): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0064 | 0/0 | 13032 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13027): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0065 | 0/0 | 13031 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13026): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0066 | 0/0 | 13033 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13028): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0067 | 0/0 | 13032 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13027): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0068 | 0/0 | 13036 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13031): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0069 | 0/0 | 13037 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13032): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0070 | 0/0 | 13036 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13031): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0071 | 0/0 | 13038 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13033): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0072 | 0/0 | 13007 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13002): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0073 | 0/1 | 13002 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12997): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0074 | 0/0 | 12999 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12994): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0075 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0076 | 0/0 | 13002 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12997): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0077 | 0/0 | 13001 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12996): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0078 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0079 | 0/0 | 13002 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12997): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0080 | 0/0 | 13003 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0081 | 0/0 | 13004 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0082 | 0/0 | 13005 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13000): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0083 | 0/0 | 13004 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0084 | 0/0 | 13005 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13000): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0085 | 0/0 | 13005 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13000): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0086 | 0/0 | 13006 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13001): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0087 | 0/0 | 13007 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13002): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0088 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0089 | 0/0 | 13004 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0090 | 0/0 | 13004 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0091 | 0/0 | 13002 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12997): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0092 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0093 | 0/0 | 13003 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0094 | 0/0 | 13009 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13004): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0095 | 0/0 | 13004 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0096 | 0/0 | 13004 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0097 | 0/0 | 13003 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0098 | 0/0 | 13001 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12996): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0099 | 0/0 | 13002 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12997): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0100 | 0/0 | 13004 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0101 | 0/0 | 13003 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0102 | 0/0 | 13003 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0103 | 0/0 | 13003 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0104 | 0/0 | 13003 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0105 | 0/0 | 13004 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0106 | 0/0 | 13004 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0107 | 0/0 | 13003 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0108 | 0/0 | 13004 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0109 | 0/0 | 13006 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13001): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0110 | 0/0 | 13008 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13003): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0111 | 0/0 | 13003 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0112 | 0/0 | 13003 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12998): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0113 | 0/0 | 13020 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13015): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0114 | 0/0 | 13006 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13001): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0115 | 0/0 | 13007 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13002): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0116 | 0/0 | 13026 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0117 | 0/0 | 13025 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13020): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0118 | 0/0 | 13026 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0119 | 0/0 | 13027 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13022): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0120 | 0/0 | 13026 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0121 | 0/0 | 13028 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13023): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0122 | 0/0 | 13019 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13014): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0123 | 0/0 | 13021 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13016): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0124 | 0/0 | 13007 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13002): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0125 | 0/0 | 13007 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13002): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0126 | 0/0 | 13008 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13003): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0127 | 0/0 | 13019 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13014): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0128 | 0/0 | 13021 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13016): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0129 | 0/0 | 13020 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13015): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0130 | 0/0 | 13021 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13016): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0131 | 0/0 | 13021 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13016): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0132 | 0/0 | 13022 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13017): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0133 | 0/0 | 13021 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13016): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0134 | 0/0 | 13022 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13017): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0135 | 0/0 | 13024 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13019): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0136 | 0/0 | 13025 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13020): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0137 | 0/0 | 13023 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13018): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0138 | 0/0 | 13025 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13020): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0139 | 0/0 | 13026 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0140 | 0/0 | 13017 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13012): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0141 | 0/0 | 13025 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13020): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0142 | 0/0 | 13031 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13026): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0143 | 0/0 | 13025 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13020): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0144 | 0/0 | 13026 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0145 | 0/0 | 13026 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0146 | 0/0 | 13025 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13020): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0147 | 0/0 | 13026 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0148 | 0/0 | 13028 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13023): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0149 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13022): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0150 | 0/0 | 13026 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0151 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13022): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0152 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13022): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0153 | 0/0 | 13028 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13023): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0154 | 0/0 | 13029 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13024): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0155 | 0/0 | 13025 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13020): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0156 | 0/0 | 13029 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13024): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0157 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13022): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0158 | 0/0 | 13029 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13024): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0159 | 0/0 | 13029 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13024): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0160 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13027): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0161 | 0/0 | 13030 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13025): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0162 | 0/0 | 13032 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13027): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0163 | 0/0 | 13021 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13016): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0164 | 0/0 | 13026 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13021): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0165 | 0/0 | 13025 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13020): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0166 | 0/0 | 13027 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13022): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0167 | 0/0 | 13004 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(12999): Show |
chr14 | 92116969 | 92177145 |
| a0001c0001t0168 | 0/0 | 13027 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTGG others(13022): Show |
chr14 | 92116969 | 92177145 |
| a0001c0003t0037 | 0/0 | 13033 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13028): Show |
chr14 | 92116969 | 92177145 |
| a0002c0002t0010 | 0/0 | 13028 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | GCTAG others(13023): Show |
chr14 | 92116969 | 92177145 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0001 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0002g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0006g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0006g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0006g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0007g0001 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0007g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0008g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0008g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0009g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0009g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0009g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0010g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0010g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0010g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0010g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0010g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0011g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0011g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0011g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0012g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0012g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0012g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0013g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0013g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0013g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0013g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0013g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0014g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0014g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0014g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0015g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0015g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0015g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0016g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0016g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0016g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0017g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0017g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0018g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0018g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0018g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0019g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0019g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0019g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0020g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0021g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0021g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0021g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0022g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0022g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0022g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0023g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0024g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0024g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0024g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0025g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0025g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0025g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0026g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0026g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0026g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0027g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0027g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0027g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0028g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0028g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0028g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0029g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0029g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0029g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0030g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0030g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0031g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0032g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0033g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0033g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0034g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0034g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0035g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0036g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0036g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0037g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0038g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0038g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0039g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0040g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0041g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0041g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0042g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0042g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0043g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0044g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0044g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0045g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0045g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0046g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0046g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0047g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0047g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0048g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0048g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0049g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0050g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0050g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0051g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0052g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0053g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0054g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0055g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0056g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0057g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0058g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0059g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0060g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0061g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0062g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0063g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0064g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0065g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0066g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0067g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0068g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0069g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0070g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0071g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0072g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0073g0159 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0074g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0075g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0076g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0077g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0078g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0079g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0080g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0081g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0082g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0083g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0084g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0085g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0086g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0087g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0088g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0089g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0090g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0091g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0092g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0093g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0094g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0095g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0096g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0097g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0098g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0099g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0100g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0101g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0102g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0103g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0104g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0105g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0106g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0107g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0108g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0109g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0110g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0111g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0112g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0113g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0114g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0115g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0116g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0117g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0118g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0119g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0120g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0121g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0122g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0123g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0124g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0125g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0126g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0127g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0128g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0129g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0130g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0131g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0132g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0133g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0134g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0135g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0136g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0137g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0138g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0139g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0140g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0141g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0142g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0143g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0144g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0145g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0146g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0147g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0148g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0149g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0150g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0151g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0152g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0153g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0154g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0155g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0156g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0157g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0158g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0159g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0160g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0161g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0162g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0163g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0164g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0165g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0166g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0167g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0001t0168g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0001c0003t0037g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| a0002c0002t0010g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0041 | g0001 | EUR | GBR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | GBR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0079 | EUR | GBR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00140 | hp2 | a0001 | c0001 | t0027 | g0228 | EUR | GBR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00323 | hp1 | a0001 | c0001 | t0167 | g0045 | EUR | FIN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0023 | EUR | FIN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00408 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00408 | hp2 | a0001 | c0001 | t0021 | g0121 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00423 | hp1 | a0001 | c0001 | t0077 | g0151 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00423 | hp2 | a0001 | c0001 | t0162 | g0007 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00438 | hp2 | a0001 | c0001 | t0145 | g0085 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00544 | hp1 | a0001 | c0001 | t0018 | g0077 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00558 | hp2 | a0001 | c0001 | t0053 | g0207 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00621 | hp1 | a0001 | c0001 | t0051 | g0014 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00621 | hp2 | a0001 | c0001 | t0009 | g0158 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00642 | hp2 | a0001 | c0001 | t0108 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00673 | hp1 | a0001 | c0001 | t0138 | g0190 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | CHS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00735 | hp1 | a0001 | c0001 | t0055 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00735 | hp2 | a0001 | c0001 | t0027 | g0227 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00738 | hp1 | a0001 | c0001 | t0104 | g0043 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG00738 | hp2 | a0001 | c0001 | t0098 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01069 | hp1 | a0001 | c0001 | t0049 | g0027 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01069 | hp2 | a0001 | c0001 | t0030 | g0232 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01071 | hp1 | a0001 | c0001 | t0049 | g0027 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01071 | hp2 | a0001 | c0001 | t0011 | g0236 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01074 | hp1 | a0001 | c0001 | t0013 | g0206 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01074 | hp2 | a0001 | c0001 | t0010 | g0010 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01081 | hp1 | a0001 | c0001 | t0010 | g0109 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01099 | hp2 | a0001 | c0001 | t0046 | g0066 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01106 | hp2 | a0001 | c0001 | t0010 | g0061 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01109 | hp1 | a0001 | c0001 | t0028 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0238 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01167 | hp2 | a0001 | c0001 | t0129 | g0209 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01168 | hp2 | a0001 | c0001 | t0166 | g0098 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01175 | hp2 | a0001 | c0001 | t0109 | g0234 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01192 | hp2 | a0001 | c0001 | t0096 | g0001 | AMR | PUR | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01255 | hp2 | a0001 | c0001 | t0074 | g0039 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01256 | hp1 | a0001 | c0001 | t0017 | g0002 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01256 | hp2 | a0001 | c0001 | t0111 | g0001 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01346 | hp1 | a0001 | c0001 | t0045 | g0191 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01361 | hp1 | a0001 | c0001 | t0105 | g0023 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01361 | hp2 | a0001 | c0001 | t0142 | g0052 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0044 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01496 | hp2 | a0001 | c0001 | t0123 | g0186 | AMR | CLM | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01515 | hp2 | a0001 | c0001 | t0011 | g0001 | EUR | IBS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01517 | hp1 | a0001 | c0001 | t0011 | g0023 | EUR | IBS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01517 | hp2 | a0001 | c0001 | t0047 | g0028 | EUR | IBS | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01884 | hp1 | a0001 | c0001 | t0122 | g0248 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01891 | hp1 | a0001 | c0001 | t0148 | g0129 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01934 | hp1 | a0001 | c0001 | t0007 | g0044 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01934 | hp2 | a0001 | c0001 | t0156 | g0073 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01975 | hp1 | a0001 | c0001 | t0045 | g0192 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0211 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG01981 | hp2 | a0001 | c0001 | t0147 | g0032 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02015 | hp1 | a0001 | c0001 | t0079 | g0153 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02015 | hp2 | a0001 | c0001 | t0163 | g0014 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0197 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02027 | hp2 | a0001 | c0001 | t0155 | g0076 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02040 | hp1 | a0001 | c0001 | t0009 | g0138 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02040 | hp2 | a0001 | c0001 | t0020 | g0011 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02055 | hp1 | a0001 | c0001 | t0086 | g0038 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02055 | hp2 | a0001 | c0001 | t0124 | g0237 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02080 | hp2 | a0001 | c0001 | t0137 | g0198 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02135 | hp1 | a0001 | c0001 | t0019 | g0089 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02135 | hp2 | a0001 | c0001 | t0038 | g0013 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02145 | hp1 | a0001 | c0001 | t0102 | g0224 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02145 | hp2 | a0001 | c0001 | t0121 | g0249 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02148 | hp1 | a0001 | c0001 | t0019 | g0086 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02155 | hp1 | a0001 | c0001 | t0051 | g0014 | EAS | CDX | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02155 | hp2 | a0001 | c0001 | t0039 | g0003 | EAS | CDX | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02165 | hp1 | a0001 | c0001 | t0021 | g0004 | EAS | CDX | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02165 | hp2 | a0001 | c0001 | t0140 | g0025 | EAS | CDX | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02257 | hp1 | a0001 | c0001 | t0095 | g0218 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02257 | hp2 | a0001 | c0001 | t0094 | g0239 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02258 | hp1 | a0001 | c0001 | t0040 | g0036 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02258 | hp2 | a0001 | c0001 | t0106 | g0047 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02273 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02280 | hp1 | a0001 | c0001 | t0017 | g0019 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02293 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02451 | hp1 | a0001 | c0001 | t0025 | g0172 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0212 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02523 | hp1 | a0001 | c0001 | t0070 | g0034 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | KHV | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0143 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02602 | hp1 | a0001 | c0001 | t0134 | g0201 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02602 | hp2 | a0001 | c0001 | t0064 | g0119 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02615 | hp1 | a0001 | c0001 | t0025 | g0038 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02615 | hp2 | a0001 | c0001 | t0017 | g0008 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02622 | hp1 | a0001 | c0001 | t0029 | g0130 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0001 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02647 | hp1 | a0001 | c0001 | t0040 | g0036 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02647 | hp2 | a0001 | c0001 | t0027 | g0001 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02683 | hp1 | a0001 | c0001 | t0046 | g0106 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02698 | hp1 | a0001 | c0001 | t0023 | g0003 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02698 | hp2 | a0001 | c0001 | t0030 | g0231 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02717 | hp2 | a0001 | c0001 | t0130 | g0202 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0254 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02735 | hp2 | a0001 | c0001 | t0017 | g0002 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02738 | hp1 | a0001 | c0001 | t0056 | g0123 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02809 | hp1 | a0001 | c0001 | t0016 | g0188 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02809 | hp2 | a0001 | c0001 | t0113 | g0245 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02895 | hp1 | a0001 | c0001 | t0043 | g0019 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02895 | hp2 | a0001 | c0001 | t0115 | g0247 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02896 | hp1 | a0001 | c0001 | t0043 | g0019 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0240 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02897 | hp1 | a0001 | c0001 | t0114 | g0246 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0242 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02922 | hp1 | a0001 | c0001 | t0117 | g0024 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02922 | hp2 | a0001 | c0001 | t0100 | g0235 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02965 | hp1 | a0001 | c0001 | t0165 | g0251 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02965 | hp2 | a0001 | c0001 | t0025 | g0171 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02970 | hp1 | a0001 | c0001 | t0119 | g0024 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02976 | hp1 | a0001 | c0001 | t0084 | g0167 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02976 | hp2 | a0001 | c0001 | t0044 | g0008 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03041 | hp2 | a0001 | c0001 | t0026 | g0148 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03098 | hp1 | a0001 | c0001 | t0082 | g0177 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03098 | hp2 | a0001 | c0001 | t0087 | g0170 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03130 | hp1 | a0001 | c0001 | t0097 | g0233 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03130 | hp2 | a0001 | c0001 | t0133 | g0187 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03139 | hp1 | a0001 | c0001 | t0022 | g0039 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03195 | hp2 | a0001 | c0001 | t0029 | g0135 | AFR | ESN | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03209 | hp1 | a0001 | c0001 | t0042 | g0250 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03209 | hp2 | a0001 | c0001 | t0048 | g0132 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03225 | hp2 | a0001 | c0001 | t0026 | g0145 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03239 | hp1 | a0001 | c0001 | t0041 | g0048 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03239 | hp2 | a0001 | c0001 | t0023 | g0003 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03453 | hp1 | a0001 | c0001 | t0110 | g0221 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03453 | hp2 | a0001 | c0001 | t0044 | g0189 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03486 | hp1 | a0001 | c0001 | t0118 | g0253 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03490 | hp1 | a0001 | c0001 | t0048 | g0108 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03491 | hp1 | a0001 | c0001 | t0065 | g0118 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03491 | hp2 | a0001 | c0001 | t0015 | g0048 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03492 | hp2 | a0001 | c0001 | t0061 | g0004 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03540 | hp2 | a0001 | c0001 | t0127 | g0199 | AFR | GWD | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03579 | hp1 | a0001 | c0001 | t0116 | g0024 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0001 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03654 | hp1 | a0001 | c0001 | t0019 | g0107 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03669 | hp1 | a0001 | c0001 | t0028 | g0243 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03669 | hp2 | a0001 | c0001 | t0101 | g0009 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03688 | hp2 | a0001 | c0001 | t0159 | g0075 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03704 | hp1 | a0001 | c0001 | t0080 | g0169 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03704 | hp2 | a0001 | c0001 | t0067 | g0114 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0195 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0194 | SAS | PJL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03831 | hp1 | a0001 | c0001 | t0132 | g0196 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03831 | hp2 | a0001 | c0001 | t0009 | g0003 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03834 | hp2 | a0001 | c0001 | t0146 | g0055 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03942 | hp1 | a0001 | c0001 | t0131 | g0183 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03942 | hp2 | a0001 | c0001 | t0112 | g0225 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG04115 | hp1 | a0001 | c0001 | t0015 | g0219 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG04115 | hp2 | a0001 | c0001 | t0083 | g0160 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG04184 | hp1 | a0001 | c0001 | t0136 | g0020 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG04184 | hp2 | a0001 | c0001 | t0139 | g0084 | SAS | BEB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0180 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG04199 | hp2 | a0001 | c0001 | t0103 | g0230 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG04204 | hp1 | a0001 | c0001 | t0023 | g0003 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG04204 | hp2 | a0001 | c0001 | t0126 | g0002 | SAS | STU | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18522 | hp1 | a0001 | c0001 | t0052 | g0040 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18612 | hp1 | a0001 | c0001 | t0063 | g0113 | EAS | CHB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0204 | EAS | CHB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18906 | hp1 | a0001 | c0001 | t0093 | g0147 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18906 | hp2 | a0001 | c0001 | t0042 | g0244 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18939 | hp1 | a0001 | c0001 | t0143 | g0007 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18941 | hp1 | a0001 | c0001 | t0128 | g0203 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18941 | hp2 | a0001 | c0001 | t0150 | g0054 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18942 | hp2 | a0001 | c0001 | t0078 | g0003 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18945 | hp1 | a0001 | c0001 | t0058 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18946 | hp1 | a0001 | c0001 | t0068 | g0116 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18948 | hp1 | a0001 | c0001 | t0033 | g0112 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18948 | hp2 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18950 | hp2 | a0001 | c0001 | t0036 | g0033 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18951 | hp1 | a0001 | c0001 | t0022 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18952 | hp1 | a0001 | c0001 | t0020 | g0011 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18952 | hp2 | a0001 | c0001 | t0149 | g0031 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18953 | hp2 | a0001 | c0001 | t0144 | g0063 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18954 | hp1 | a0001 | c0001 | t0164 | g0139 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18954 | hp2 | a0001 | c0001 | t0057 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18956 | hp1 | a0001 | c0001 | t0021 | g0122 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18957 | hp1 | a0001 | c0001 | t0008 | g0154 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18959 | hp2 | a0001 | c0001 | t0092 | g0003 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18961 | hp1 | a0001 | c0001 | t0009 | g0144 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18961 | hp2 | a0001 | c0001 | t0018 | g0072 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18962 | hp2 | a0001 | c0001 | t0038 | g0137 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18964 | hp1 | a0001 | c0001 | t0075 | g0013 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18964 | hp2 | a0001 | c0003 | t0037 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18966 | hp1 | a0001 | c0001 | t0008 | g0150 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18968 | hp2 | a0001 | c0001 | t0024 | g0152 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18969 | hp1 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18971 | hp1 | a0001 | c0001 | t0031 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18972 | hp1 | a0001 | c0001 | t0135 | g0184 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18972 | hp2 | a0001 | c0001 | t0024 | g0017 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18977 | hp2 | a0001 | c0001 | t0050 | g0029 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0030 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18980 | hp1 | a0001 | c0001 | t0034 | g0033 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18981 | hp1 | a0001 | c0001 | t0018 | g0060 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18981 | hp2 | a0001 | c0001 | t0013 | g0042 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18982 | hp1 | a0001 | c0001 | t0072 | g0117 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18982 | hp2 | a0001 | c0001 | t0016 | g0126 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18984 | hp1 | a0001 | c0001 | t0157 | g0100 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18984 | hp2 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18986 | hp2 | a0001 | c0001 | t0013 | g0181 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18988 | hp1 | a0001 | c0001 | t0154 | g0088 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18988 | hp2 | a0001 | c0001 | t0125 | g0185 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18989 | hp1 | a0001 | c0001 | t0032 | g0035 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18989 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18991 | hp2 | a0001 | c0001 | t0054 | g0208 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18993 | hp1 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18995 | hp1 | a0001 | c0001 | t0089 | g0017 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18997 | hp1 | a0001 | c0001 | t0066 | g0110 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18998 | hp1 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA18999 | hp2 | a0001 | c0001 | t0016 | g0127 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19000 | hp2 | a0001 | c0001 | t0013 | g0210 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19001 | hp1 | a0001 | c0001 | t0158 | g0067 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19001 | hp2 | a0001 | c0001 | t0032 | g0035 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19003 | hp1 | a0001 | c0001 | t0037 | g0124 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19003 | hp2 | a0001 | c0001 | t0151 | g0062 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19007 | hp1 | a0001 | c0001 | t0033 | g0034 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19007 | hp2 | a0001 | c0001 | t0010 | g0095 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19009 | hp2 | a0001 | c0001 | t0035 | g0016 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19010 | hp1 | a0001 | c0001 | t0050 | g0097 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19011 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19011 | hp2 | a0001 | c0001 | t0024 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19030 | hp1 | a0001 | c0001 | t0085 | g0149 | AFR | LWK | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19030 | hp2 | a0001 | c0001 | t0029 | g0131 | AFR | LWK | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19054 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19054 | hp2 | a0001 | c0001 | t0071 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19055 | hp1 | a0001 | c0001 | t0088 | g0155 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19055 | hp2 | a0001 | c0001 | t0060 | g0111 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19056 | hp1 | a0001 | c0001 | t0012 | g0125 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19056 | hp2 | a0001 | c0001 | t0107 | g0226 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19058 | hp1 | a0001 | c0001 | t0062 | g0120 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19058 | hp2 | a0001 | c0001 | t0022 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19060 | hp1 | a0001 | c0001 | t0034 | g0101 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19060 | hp2 | a0001 | c0001 | t0039 | g0003 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19062 | hp1 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19063 | hp2 | a0001 | c0001 | t0160 | g0065 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19064 | hp1 | a0001 | c0001 | t0091 | g0012 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19064 | hp2 | a0001 | c0001 | t0020 | g0011 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19065 | hp2 | a0001 | c0001 | t0152 | g0015 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19066 | hp2 | a0001 | c0001 | t0010 | g0092 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19074 | hp1 | a0001 | c0001 | t0069 | g0115 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19075 | hp1 | a0001 | c0001 | t0168 | g0083 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19077 | hp1 | a0002 | c0002 | t0010 | g0080 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19079 | hp1 | a0001 | c0001 | t0036 | g0016 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19081 | hp1 | a0001 | c0001 | t0081 | g0013 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19081 | hp2 | a0001 | c0001 | t0047 | g0087 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19083 | hp1 | a0001 | c0001 | t0035 | g0016 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19083 | hp2 | a0001 | c0001 | t0013 | g0182 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19084 | hp1 | a0001 | c0001 | t0031 | g0004 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19087 | hp1 | a0001 | c0001 | t0153 | g0025 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19088 | hp1 | a0001 | c0001 | t0019 | g0093 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19090 | hp1 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19090 | hp2 | a0001 | c0001 | t0009 | g0005 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19091 | hp2 | a0001 | c0001 | t0059 | g0011 | EAS | JPT | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0168 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | YRI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA20129 | hp1 | a0001 | c0001 | t0141 | g0134 | AFR | ASW | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA20129 | hp2 | a0001 | c0001 | t0120 | g0252 | AFR | ASW | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA20752 | hp2 | a0001 | c0001 | t0010 | g0081 | EUR | TSI | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | GIH | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA20905 | hp2 | a0001 | c0001 | t0076 | g0161 | SAS | GIH | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02486 | hp1 | a0001 | c0001 | t0099 | g0220 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02486 | hp2 | a0001 | c0001 | t0026 | g0146 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0241 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG02559 | hp2 | a0001 | c0001 | t0028 | g0223 | AFR | ACB | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03471 | hp1 | a0001 | c0001 | t0090 | g0173 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG03471 | hp2 | a0001 | c0001 | t0016 | g0193 | AFR | MSL | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG06807 | hp1 | a0001 | c0001 | t0052 | g0040 | AFR | USA | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | USA | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| NA20300 | hp2 | a0001 | c0001 | t0161 | g0032 | AFR | USA | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0073 | g0159 | REF | REF | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0229 | REF | REF | CPSF2_chr14_92116969_92177145 | CPSF2 | chr14 | 92116969 | 92177145 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:92156503 | G | C | 1 | a0002 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.1467G>C | p.Glu489Asp | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/16 | 1720/13003 | 1467/2349 | 489/782 | chr14 | 92156503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:92157767 | A | G | 1 | a0001c0003 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.1704A>G | p.Pro568Pro | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/16 | 1957/13003 | 1704/2349 | 568/782 | chr14 | 92157767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:92121972 | A | G | 1 | a0001c0001t0168 | 1 | NA19075.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-250A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/16 | chr14 | 92121972 | |||||||
| chr14:92122070 | C | T | 1 | a0001c0001t0052 | 2 | HG06807.hp1 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-152C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/16 | 8915 | chr14 | 92122070 | ||||||
| chr14:92161944 | G | A | 2 | a0001c0001t0053 a0001c0001t0054 |
2 | HG00558.hp2 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 200 | chr14 | 92161944 | ||||||
| chr14:92162012 | T | C | 1 | a0001c0001t0030 | 2 | HG01069.hp2 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*268T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 268 | chr14 | 92162012 | ||||||
| chr14:92162110 | G | A | 1 | a0001c0001t0055 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*366G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 366 | chr14 | 92162110 | ||||||
| chr14:92162272 | G | A | 1 | a0001c0001t0031 | 2 | NA18971.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*528G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 528 | chr14 | 92162272 | ||||||
| chr14:92162315 | A | G | 1 | a0001c0001t0167 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*571A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 571 | chr14 | 92162315 | ||||||
| chr14:92162339 | A | G | 1 | a0001c0001t0166 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*595A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 595 | chr14 | 92162339 | ||||||
| chr14:92162404 | A | G | 1 | a0001c0001t0165 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 660 | chr14 | 92162404 | ||||||
| chr14:92162534 | G | A | 27 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0031 others(24): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*790G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 790 | chr14 | 92162534 | ||||||
| chr14:92162608 | T | G | 32 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(29): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*864T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 864 | chr14 | 92162608 | ||||||
| chr14:92162974 | G | T | 1 | a0001c0001t0164 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1230G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1230 | chr14 | 92162974 | ||||||
| chr14:92163008 | A | G | 1 | a0001c0001t0040 | 2 | HG02258.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1264A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1264 | chr14 | 92163008 | ||||||
| chr14:92163044 | C | T | 2 | a0001c0001t0026 a0001c0001t0093 |
4 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1300C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1300 | chr14 | 92163044 | ||||||
| chr14:92163337 | C | A | 2 | a0001c0001t0014 a0001c0001t0094 |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1593C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1593 | chr14 | 92163337 | ||||||
| chr14:92163366 | C | T | 2 | a0001c0001t0051 a0001c0001t0163 |
3 | HG00621.hp1 HG02015.hp2 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1622C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1622 | chr14 | 92163366 | ||||||
| chr14:92163371 | T | TAAAC | 75 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(72): Show |
180 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1630_*1631insCAAA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1631 | INFO_REALIGN_3_PRIME | chr14 | 92163371 | |||||
| chr14:92163373 | A | AACAC | 63 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(60): Show |
130 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1630_*1631insCACA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1631 | INFO_REALIGN_3_PRIME | chr14 | 92163373 | |||||
| chr14:92163374 | A | AC | 3 | a0001c0001t0037 a0001c0001t0072 a0001c0003t0037 |
3 | NA18964.hp2 NA18982.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1630_*1631insC | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1631 | chr14 | 92163374 | ||||||
| chr14:92163378 | A | G | 1 | a0001c0001t0092 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1634A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1634 | chr14 | 92163378 | ||||||
| chr14:92163379 | T | C | 3 | a0001c0001t0037 a0001c0001t0072 a0001c0003t0037 |
3 | NA18964.hp2 NA18982.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1635T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1635 | chr14 | 92163379 | ||||||
| chr14:92163420 | T | A | 1 | a0001c0001t0095 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1676T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1676 | chr14 | 92163420 | ||||||
| chr14:92163472 | T | C | 12 | a0001c0001t0042 a0001c0001t0113 a0001c0001t0114 others(9): Show |
13 | HG01884.hp1 HG02145.hp2 HG02809.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1728T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1728 | chr14 | 92163472 | ||||||
| chr14:92163563 | A | G | 2 | a0001c0001t0014 a0001c0001t0094 |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1819A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1819 | chr14 | 92163563 | ||||||
| chr14:92163599 | A | G | 1 | a0001c0001t0091 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1855 | chr14 | 92163599 | ||||||
| chr14:92163635 | C | T | 78 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(75): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1891C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1891 | chr14 | 92163635 | ||||||
| chr14:92163722 | T | G | 2 | a0001c0001t0014 a0001c0001t0094 |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1978T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 1978 | chr14 | 92163722 | ||||||
| chr14:92163807 | C | T | 2 | a0001c0001t0041 a0001c0001t0112 |
3 | HG00099.hp1 HG03239.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2063C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2063 | chr14 | 92163807 | ||||||
| chr14:92163834 | G | A | 2 | a0001c0001t0027 a0001c0001t0096 |
4 | HG00140.hp2 HG00735.hp2 HG01192.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2090G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2090 | chr14 | 92163834 | ||||||
| chr14:92163888 | G | A | 1 | a0001c0001t0123 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2144G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2144 | chr14 | 92163888 | ||||||
| chr14:92163947 | C | T | 1 | a0001c0001t0045 | 2 | HG01346.hp1 HG01975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2203C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2203 | chr14 | 92163947 | ||||||
| chr14:92163982 | G | A | 32 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(29): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2238G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2238 | chr14 | 92163982 | ||||||
| chr14:92164025 | T | C | 27 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0031 others(24): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2281T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2281 | chr14 | 92164025 | ||||||
| chr14:92164063 | C | T | 1 | a0001c0001t0112 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2319C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2319 | chr14 | 92164063 | ||||||
| chr14:92164226 | C | T | 2 | a0001c0001t0014 a0001c0001t0094 |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2482C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2482 | chr14 | 92164226 | ||||||
| chr14:92164267 | T | G | 1 | a0001c0001t0097 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2523T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2523 | chr14 | 92164267 | ||||||
| chr14:92164581 | G | T | 2 | a0001c0001t0137 a0001c0001t0138 |
2 | HG00673.hp1 HG02080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2837G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2837 | chr14 | 92164581 | ||||||
| chr14:92164621 | T | A | 141 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(138): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*2877T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 2877 | chr14 | 92164621 | ||||||
| chr14:92165025 | C | A | 1 | a0001c0001t0056 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3281C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3281 | chr14 | 92165025 | ||||||
| chr14:92165123 | A | G | 1 | a0001c0001t0090 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3379A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3379 | chr14 | 92165123 | ||||||
| chr14:92165198 | A | C | 1 | a0001c0001t0052 | 2 | HG06807.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3454A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3454 | chr14 | 92165198 | ||||||
| chr14:92165232 | C | G | 11 | a0001c0001t0042 a0001c0001t0114 a0001c0001t0115 others(8): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3488C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3488 | chr14 | 92165232 | ||||||
| chr14:92165235 | G | A | 1 | a0001c0001t0113 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3491G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3491 | chr14 | 92165235 | ||||||
| chr14:92165241 | G | GT | 67 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(64): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*3510dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3511 | INFO_REALIGN_3_PRIME | chr14 | 92165241 | |||||
| chr14:92165241 | GT | G | 3 | a0001c0001t0014 a0001c0001t0094 a0001c0001t0163 |
6 | HG01109.hp2 HG02015.hp2 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3510delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3510 | INFO_REALIGN_3_PRIME | chr14 | 92165241 | |||||
| chr14:92165334 | C | A | 11 | a0001c0001t0042 a0001c0001t0114 a0001c0001t0115 others(8): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3590C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3590 | chr14 | 92165334 | ||||||
| chr14:92165521 | G | A | 1 | a0001c0001t0093 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3777G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3777 | chr14 | 92165521 | ||||||
| chr14:92165546 | A | G | 2 | a0001c0001t0014 a0001c0001t0094 |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3802A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3802 | chr14 | 92165546 | ||||||
| chr14:92165597 | T | G | 1 | a0001c0001t0124 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3853T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3853 | chr14 | 92165597 | ||||||
| chr14:92165610 | A | G | 61 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(58): Show |
162 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*3866A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3866 | chr14 | 92165610 | ||||||
| chr14:92165725 | G | A | 141 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(138): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*3981G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 3981 | chr14 | 92165725 | ||||||
| chr14:92165766 | G | A | 2 | a0001c0001t0014 a0001c0001t0094 |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4022G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4022 | chr14 | 92165766 | ||||||
| chr14:92165854 | C | CT | 7 | a0001c0001t0021 a0001c0001t0028 a0001c0001t0072 others(4): Show |
11 | HG00408.hp2 HG01109.hp1 HG01175.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4135dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTT | 16 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0023 others(13): Show |
59 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*4132_*4135dupTTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTT | 10 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0025 others(7): Show |
22 | HG00621.hp2 HG01109.hp2 HG02040.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4131_*4135dupTTTT others(1): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTT | 5 | a0001c0001t0026 a0001c0001t0085 a0001c0001t0086 others(2): Show |
7 | HG02055.hp1 HG02486.hp2 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4130_*4135dupTTTT others(2): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(2): Show |
5 | a0001c0001t0042 a0001c0001t0116 a0001c0001t0117 others(2): Show |
6 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4127_*4135dupTTTT others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0113 a0001c0001t0119 a0001c0001t0120 |
3 | HG02809.hp2 HG02970.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4126_*4135dupTTTT others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0121 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4125_*4135dupTTTT others(7): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(5): Show |
5 | a0001c0001t0043 a0001c0001t0122 a0001c0001t0127 others(2): Show |
6 | HG01361.hp2 HG01884.hp1 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4124_*4135dupTTTT others(8): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(6): Show |
18 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0017 others(15): Show |
45 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*4123_*4135dupTTTT others(9): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(7): Show |
17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0012 others(14): Show |
62 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*4122_*4135dupTTTT others(10): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(8): Show |
12 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0019 others(9): Show |
31 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4121_*4135dupTTTT others(11): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(9): Show |
8 | a0001c0001t0013 a0001c0001t0049 a0001c0001t0050 others(5): Show |
15 | HG00621.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4120_*4135dupTTTT others(12): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0161 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4119_*4135dupTTTT others(13): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0136 a0001c0001t0138 a0001c0001t0162 |
3 | HG00423.hp2 HG00673.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4118_*4135dupTTTT others(14): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(14): Show |
4 | a0001c0001t0060 a0001c0001t0061 a0001c0001t0062 others(1): Show |
4 | HG03492.hp2 NA18612.hp1 NA19055.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4115_*4135dupTTTT others(17): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(15): Show |
3 | a0001c0001t0034 a0001c0001t0064 a0001c0001t0065 |
4 | HG02602.hp2 HG03491.hp1 NA18980.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4114_*4135dupTTTT others(18): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(16): Show |
3 | a0001c0001t0035 a0001c0001t0066 a0001c0001t0067 |
4 | HG03704.hp2 NA18997.hp1 NA19009.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4113_*4135dupTTTT others(19): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0056 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4112_*4135dupTTTT others(20): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0068 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4135_*4136insTTTT others(22): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(20): Show |
5 | a0001c0001t0037 a0001c0001t0069 a0001c0001t0070 others(2): Show |
5 | HG02523.hp1 NA18964.hp2 NA19003.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4135_*4136insTTTT others(23): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0036 | 2 | NA18950.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4135_*4136insTTTT others(24): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4136 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165854 | CT | C | 4 | a0001c0001t0015 a0001c0001t0046 a0001c0001t0059 others(1): Show |
8 | HG01099.hp2 HG01256.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4135delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4135 | INFO_REALIGN_3_PRIME | chr14 | 92165854 | |||||
| chr14:92165892 | T | C | 141 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(138): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*4148T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4148 | chr14 | 92165892 | ||||||
| chr14:92165965 | G | T | 1 | a0001c0001t0079 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4221G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4221 | chr14 | 92165965 | ||||||
| chr14:92166115 | G | T | 32 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(29): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*4371G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4371 | chr14 | 92166115 | ||||||
| chr14:92166146 | G | C | 1 | a0001c0001t0113 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4402G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4402 | chr14 | 92166146 | ||||||
| chr14:92166406 | G | A | 2 | a0001c0001t0014 a0001c0001t0094 |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4662G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4662 | chr14 | 92166406 | ||||||
| chr14:92166540 | T | G | 141 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(138): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*4796T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4796 | chr14 | 92166540 | ||||||
| chr14:92166682 | T | C | 1 | a0001c0001t0159 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4938T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 4938 | chr14 | 92166682 | ||||||
| chr14:92166843 | T | C | 29 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(26): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*5099T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5099 | chr14 | 92166843 | ||||||
| chr14:92166982 | G | A | 11 | a0001c0001t0042 a0001c0001t0114 a0001c0001t0115 others(8): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5238G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5238 | chr14 | 92166982 | ||||||
| chr14:92167014 | C | CT | 52 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(49): Show |
116 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*5285dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5286 | INFO_REALIGN_3_PRIME | chr14 | 92167014 | |||||
| chr14:92167014 | C | CTT | 46 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(43): Show |
95 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*5284_*5285dupTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5286 | INFO_REALIGN_3_PRIME | chr14 | 92167014 | |||||
| chr14:92167014 | C | CTTT | 9 | a0001c0001t0025 a0001c0001t0029 a0001c0001t0048 others(6): Show |
14 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5283_*5285dupTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5286 | INFO_REALIGN_3_PRIME | chr14 | 92167014 | |||||
| chr14:92167014 | C | CTTTT | 33 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(30): Show |
87 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*5282_*5285dupTTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5286 | INFO_REALIGN_3_PRIME | chr14 | 92167014 | |||||
| chr14:92167068 | A | G | 141 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(138): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*5324A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5324 | chr14 | 92167068 | ||||||
| chr14:92167097 | C | T | 1 | a0001c0001t0078 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5353C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5353 | chr14 | 92167097 | ||||||
| chr14:92167158 | C | T | 1 | a0001c0001t0079 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5414C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5414 | chr14 | 92167158 | ||||||
| chr14:92167192 | A | G | 1 | a0001c0001t0084 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5448A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5448 | chr14 | 92167192 | ||||||
| chr14:92167254 | C | T | 1 | a0001c0001t0148 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5510C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5510 | chr14 | 92167254 | ||||||
| chr14:92167533 | T | C | 1 | a0001c0001t0084 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5789T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5789 | chr14 | 92167533 | ||||||
| chr14:92167628 | T | TA | 39 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(36): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*5884_*5885insA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5885 | chr14 | 92167628 | ||||||
| chr14:92167630 | A | T | 39 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(36): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*5886A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5886 | chr14 | 92167630 | ||||||
| chr14:92167670 | G | A | 141 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(138): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*5926G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 5926 | chr14 | 92167670 | ||||||
| chr14:92167770 | TTAATG | T | 32 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(29): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*6030_*6034delTGTA others(1): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6030 | INFO_REALIGN_3_PRIME | chr14 | 92167770 | |||||
| chr14:92167797 | G | C | 1 | a0001c0001t0040 | 2 | HG02258.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6053G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6053 | chr14 | 92167797 | ||||||
| chr14:92167844 | G | A | 8 | a0001c0001t0042 a0001c0001t0116 a0001c0001t0117 others(5): Show |
9 | HG02145.hp2 HG02922.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6100G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6100 | chr14 | 92167844 | ||||||
| chr14:92167850 | A | G | 1 | a0001c0001t0068 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6106A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6106 | chr14 | 92167850 | ||||||
| chr14:92167889 | C | T | 1 | a0001c0001t0107 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6145C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6145 | chr14 | 92167889 | ||||||
| chr14:92167892 | G | GT | 31 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(28): Show |
77 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*6166dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6167 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | |||||
| chr14:92167892 | G | GTT | 26 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0022 others(23): Show |
74 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*6165_*6166dupTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6167 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | |||||
| chr14:92167892 | G | GTTT | 5 | a0001c0001t0008 a0001c0001t0084 a0001c0001t0087 others(2): Show |
12 | HG02572.hp1 HG02976.hp1 HG03098.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6164_*6166dupTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6167 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | |||||
| chr14:92167892 | GT | G | 16 | a0001c0001t0014 a0001c0001t0042 a0001c0001t0050 others(13): Show |
21 | HG00738.hp2 HG01109.hp2 HG02257.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6166delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6166 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | |||||
| chr14:92167892 | GTT | G | 61 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(58): Show |
127 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*6165_*6166delTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6165 | INFO_REALIGN_3_PRIME | chr14 | 92167892 | |||||
| chr14:92167898 | T | G | 2 | a0001c0001t0144 a0001c0001t0145 |
2 | HG00438.hp2 NA18953.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6154T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6154 | chr14 | 92167898 | ||||||
| chr14:92167900 | T | G | 2 | a0001c0001t0014 a0001c0001t0094 |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6156T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6156 | chr14 | 92167900 | ||||||
| chr14:92168061 | A | G | 1 | a0001c0001t0040 | 2 | HG02258.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6317A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6317 | chr14 | 92168061 | ||||||
| chr14:92168078 | C | T | 78 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(75): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*6334C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6334 | chr14 | 92168078 | ||||||
| chr14:92168102 | G | A | 1 | a0001c0001t0098 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6358G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6358 | chr14 | 92168102 | ||||||
| chr14:92168227 | G | A | 2 | a0001c0001t0099 a0001c0001t0100 |
2 | HG02486.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6483G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6483 | chr14 | 92168227 | ||||||
| chr14:92168229 | C | T | 32 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(29): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*6485C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6485 | chr14 | 92168229 | ||||||
| chr14:92168248 | C | CAAAAAAA | 6 | a0001c0001t0042 a0001c0001t0113 a0001c0001t0117 others(3): Show |
7 | HG02809.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6516_*6522dupAAAA others(3): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | |||||
| chr14:92168248 | C | CAAAAAAA others(1): Show |
48 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(45): Show |
104 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*6515_*6522dupAAAA others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | |||||
| chr14:92168248 | C | CAAAAAAA others(2): Show |
19 | a0001c0001t0018 a0001c0001t0019 a0001c0001t0029 others(16): Show |
30 | HG00423.hp2 HG00544.hp1 HG01517.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6514_*6522dupAAAA others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | |||||
| chr14:92168248 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0148 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6513_*6522dupAAAA others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | |||||
| chr14:92168248 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0142 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6510_*6522dupAAAA others(9): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6523 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | |||||
| chr14:92168248 | CA | C | 55 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(52): Show |
157 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*6522delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6522 | INFO_REALIGN_3_PRIME | chr14 | 92168248 | |||||
| chr14:92168350 | T | A | 39 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(36): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*6606T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6606 | chr14 | 92168350 | ||||||
| chr14:92168413 | A | T | 29 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(26): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*6669A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6669 | chr14 | 92168413 | ||||||
| chr14:92168523 | C | T | 3 | a0001c0001t0025 a0001c0001t0086 a0001c0001t0087 |
5 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6779C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6779 | chr14 | 92168523 | ||||||
| chr14:92168577 | A | G | 3 | a0001c0001t0025 a0001c0001t0086 a0001c0001t0087 |
5 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6833A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6833 | chr14 | 92168577 | ||||||
| chr14:92168627 | C | T | 1 | a0001c0001t0147 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6883C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 6883 | chr14 | 92168627 | ||||||
| chr14:92168744 | A | G | 1 | a0001c0001t0071 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7000A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7000 | chr14 | 92168744 | ||||||
| chr14:92168799 | G | A | 2 | a0001c0001t0023 a0001c0001t0076 |
4 | HG02698.hp1 HG03239.hp2 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7055G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7055 | chr14 | 92168799 | ||||||
| chr14:92168837 | A | T | 1 | a0001c0001t0156 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7093A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7093 | chr14 | 92168837 | ||||||
| chr14:92168884 | G | A | 1 | a0001c0001t0080 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7140G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7140 | chr14 | 92168884 | ||||||
| chr14:92169099 | AAAG | A | 67 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(64): Show |
134 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*7359_*7361delAAG | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7359 | INFO_REALIGN_3_PRIME | chr14 | 92169099 | |||||
| chr14:92169119 | G | A | 1 | a0001c0001t0084 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7375G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7375 | chr14 | 92169119 | ||||||
| chr14:92169184 | T | C | 1 | a0001c0001t0088 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7440T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7440 | chr14 | 92169184 | ||||||
| chr14:92169421 | ATAAC | A | 31 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(28): Show |
89 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*7681_*7684delCTAA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7681 | INFO_REALIGN_3_PRIME | chr14 | 92169421 | |||||
| chr14:92169527 | A | T | 2 | a0001c0001t0057 a0001c0001t0058 |
2 | NA18945.hp1 NA18954.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7783A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7783 | chr14 | 92169527 | ||||||
| chr14:92169629 | T | C | 142 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(139): Show |
314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*7885T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7885 | chr14 | 92169629 | ||||||
| chr14:92169631 | A | G | 3 | a0001c0001t0061 a0001c0001t0065 a0001c0001t0067 |
3 | HG03491.hp1 HG03492.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7887A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7887 | chr14 | 92169631 | ||||||
| chr14:92169649 | A | AT | 11 | a0001c0001t0055 a0001c0001t0100 a0001c0001t0105 others(8): Show |
11 | HG00323.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7927dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7928 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | |||||
| chr14:92169649 | AT | A | 13 | a0001c0001t0011 a0001c0001t0014 a0001c0001t0024 others(10): Show |
22 | HG01071.hp2 HG01109.hp2 HG01515.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*7927delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7927 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | |||||
| chr14:92169649 | ATT | A | 51 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(48): Show |
142 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*7926_*7927delTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7926 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | |||||
| chr14:92169649 | ATTT | A | 63 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(60): Show |
137 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*7925_*7927delTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7925 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | |||||
| chr14:92169649 | ATTTT | A | 7 | a0001c0001t0049 a0001c0001t0057 a0001c0001t0142 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG01361.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7924_*7927delTTTT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 7924 | INFO_REALIGN_3_PRIME | chr14 | 92169649 | |||||
| chr14:92169810 | A | C | 1 | a0001c0001t0064 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8066A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8066 | chr14 | 92169810 | ||||||
| chr14:92169885 | C | T | 3 | a0001c0001t0114 a0001c0001t0115 a0001c0001t0122 |
3 | HG01884.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8141C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8141 | chr14 | 92169885 | ||||||
| chr14:92169892 | C | T | 1 | a0001c0001t0075 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8148C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8148 | chr14 | 92169892 | ||||||
| chr14:92169972 | T | A | 1 | a0001c0001t0023 | 3 | HG02698.hp1 HG03239.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8228T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8228 | chr14 | 92169972 | ||||||
| chr14:92170077 | G | A | 39 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(36): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*8333G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8333 | chr14 | 92170077 | ||||||
| chr14:92170084 | A | G | 1 | a0001c0001t0131 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8340A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8340 | chr14 | 92170084 | ||||||
| chr14:92170089 | G | A | 11 | a0001c0001t0042 a0001c0001t0114 a0001c0001t0115 others(8): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*8345G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8345 | chr14 | 92170089 | ||||||
| chr14:92170097 | A | T | 6 | a0001c0001t0116 a0001c0001t0117 a0001c0001t0118 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8353A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8353 | chr14 | 92170097 | ||||||
| chr14:92170332 | T | G | 78 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(75): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*8588T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8588 | chr14 | 92170332 | ||||||
| chr14:92170369 | A | T | 61 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(58): Show |
162 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*8625A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8625 | chr14 | 92170369 | ||||||
| chr14:92170590 | C | G | 30 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(27): Show |
73 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*8846C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8846 | chr14 | 92170590 | ||||||
| chr14:92170739 | G | A | 27 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0031 others(24): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*8995G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 8995 | chr14 | 92170739 | ||||||
| chr14:92170759 | A | G | 1 | a0001c0001t0104 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9015A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9015 | chr14 | 92170759 | ||||||
| chr14:92170802 | G | C | 1 | a0001c0001t0102 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9058G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9058 | chr14 | 92170802 | ||||||
| chr14:92170899 | C | T | 78 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(75): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*9155C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9155 | chr14 | 92170899 | ||||||
| chr14:92171006 | G | A | 3 | a0001c0001t0014 a0001c0001t0094 a0001c0001t0151 |
6 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9262G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9262 | chr14 | 92171006 | ||||||
| chr14:92171164 | T | C | 1 | a0001c0001t0152 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9420T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9420 | chr14 | 92171164 | ||||||
| chr14:92171167 | C | T | 1 | a0001c0001t0152 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9423C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9423 | chr14 | 92171167 | ||||||
| chr14:92171203 | T | A | 1 | a0001c0001t0085 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9459T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9459 | chr14 | 92171203 | ||||||
| chr14:92171234 | T | C | 142 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(139): Show |
314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*9490T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9490 | chr14 | 92171234 | ||||||
| chr14:92171342 | T | C | 1 | a0001c0001t0113 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9598T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9598 | chr14 | 92171342 | ||||||
| chr14:92171443 | T | C | 1 | a0001c0001t0103 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9699T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9699 | chr14 | 92171443 | ||||||
| chr14:92171556 | T | C | 27 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0031 others(24): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*9812T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9812 | chr14 | 92171556 | ||||||
| chr14:92171624 | C | T | 1 | a0001c0001t0127 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9880C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9880 | chr14 | 92171624 | ||||||
| chr14:92171625 | G | A | 1 | a0001c0001t0134 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9881G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9881 | chr14 | 92171625 | ||||||
| chr14:92171675 | G | A | 1 | a0001c0001t0144 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9931G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9931 | chr14 | 92171675 | ||||||
| chr14:92171703 | T | C | 1 | a0001c0001t0064 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9959T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9959 | chr14 | 92171703 | ||||||
| chr14:92171708 | G | A | 4 | a0001c0001t0025 a0001c0001t0086 a0001c0001t0087 others(1): Show |
6 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9964G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 9964 | chr14 | 92171708 | ||||||
| chr14:92172041 | G | T | 1 | a0001c0001t0129 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10297G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 10297 | chr14 | 92172041 | ||||||
| chr14:92172098 | A | G | 32 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(29): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*10354A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 10354 | chr14 | 92172098 | ||||||
| chr14:92172124 | A | G | 142 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(139): Show |
314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*10380A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 16/16 | 10380 | chr14 | 92172124 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:92122151 | A | G | 1 | a0001c0001t0003g0254 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-94+23A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122151 | |||||||
| chr14:92122250 | C | T | 1 | a0001c0001t0118g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-94+122C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122250 | |||||||
| chr14:92122266 | G | T | 1 | a0001c0001t0003g0254 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-94+138G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122266 | |||||||
| chr14:92122330 | C | G | 13 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0113g0245 others(10): Show |
13 | HG01884.hp1 HG02145.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.-94+202C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122330 | |||||||
| chr14:92122344 | G | A | 86 | a0001c0001t0001g0105 a0001c0001t0003g0007 a0001c0001t0003g0010 others(83): Show |
89 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-94+216G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122344 | |||||||
| chr14:92122383 | C | T | 1 | a0001c0001t0028g0243 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-94+255C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122383 | |||||||
| chr14:92122467 | G | C | 34 | a0001c0001t0012g0125 a0001c0001t0016g0126 a0001c0001t0016g0127 others(31): Show |
39 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(36): Show |
intron_variant | MODIFIER | c.-94+339G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122467 | |||||||
| chr14:92122573 | T | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
239 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-94+445T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122573 | |||||||
| chr14:92122644 | C | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+516C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122644 | |||||||
| chr14:92122654 | C | T | 5 | a0001c0001t0003g0254 a0001c0001t0010g0109 a0001c0001t0019g0107 others(2): Show |
5 | HG01081.hp1 HG02683.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+526C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122654 | |||||||
| chr14:92122677 | C | A | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+549C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122677 | |||||||
| chr14:92122708 | A | AT | 75 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.-94+584dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92122708 | ||||||
| chr14:92122763 | T | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
239 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-94+635T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122763 | |||||||
| chr14:92122853 | C | CT | 88 | a0001c0001t0001g0179 a0001c0001t0003g0007 a0001c0001t0003g0010 others(85): Show |
91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-94+740dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92122853 | ||||||
| chr14:92122853 | C | CTT | 6 | a0001c0001t0003g0103 a0001c0001t0003g0104 a0001c0001t0004g0102 others(3): Show |
6 | HG00673.hp2 HG01433.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-94+739_-94+740dup others(2): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92122853 | ||||||
| chr14:92122868 | T | A | 1 | a0001c0001t0042g0244 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-94+740T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92122868 | |||||||
| chr14:92122868 | T | TA | 12 | a0001c0001t0042g0250 a0001c0001t0113g0245 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-94+742dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92122868 | ||||||
| chr14:92123004 | G | A | 53 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(50): Show |
68 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-94+876G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123004 | |||||||
| chr14:92123093 | G | T | 1 | a0001c0001t0052g0040 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-94+965G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123093 | |||||||
| chr14:92123149 | A | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-94+1021A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123149 | |||||||
| chr14:92123156 | C | G | 2 | a0001c0001t0034g0101 a0001c0001t0157g0100 |
2 | NA18984.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-94+1028C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123156 | |||||||
| chr14:92123197 | C | T | 1 | a0001c0001t0005g0213 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-94+1069C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123197 | |||||||
| chr14:92123384 | G | T | 54 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(51): Show |
69 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-94+1256G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123384 | |||||||
| chr14:92123414 | T | C | 6 | a0001c0001t0034g0033 a0001c0001t0035g0016 a0001c0001t0036g0016 others(3): Show |
7 | NA18950.hp2 NA18980.hp1 NA18997.hp1 others(4): Show |
intron_variant | MODIFIER | c.-94+1286T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123414 | |||||||
| chr14:92123421 | C | T | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-94+1293C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123421 | |||||||
| chr14:92123598 | CAT | C | 34 | a0001c0001t0012g0125 a0001c0001t0016g0126 a0001c0001t0016g0127 others(31): Show |
39 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(36): Show |
intron_variant | MODIFIER | c.-94+1473_-94+1474d others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92123598 | ||||||
| chr14:92123776 | C | T | 140 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(137): Show |
148 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.-94+1648C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123776 | |||||||
| chr14:92123848 | A | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.-94+1720A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123848 | |||||||
| chr14:92123866 | A | G | 1 | a0001c0001t0011g0236 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-94+1738A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123866 | |||||||
| chr14:92123922 | T | A | 2 | a0001c0001t0001g0136 a0001c0001t0038g0137 |
2 | NA18962.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-94+1794T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92123922 | |||||||
| chr14:92124220 | T | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
239 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-93-1902T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124220 | |||||||
| chr14:92124278 | T | C | 10 | a0001c0001t0005g0018 a0001c0001t0006g0014 a0001c0001t0006g0018 others(7): Show |
12 | HG00621.hp1 HG02015.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.-93-1844T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124278 | |||||||
| chr14:92124495 | T | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
91 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.-93-1627T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124495 | |||||||
| chr14:92124513 | G | A | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-1609G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124513 | |||||||
| chr14:92124809 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-93-1313A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124809 | |||||||
| chr14:92124948 | G | A | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-1174G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92124948 | |||||||
| chr14:92125049 | T | G | 1 | a0001c0001t0009g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-93-1073T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125049 | |||||||
| chr14:92125196 | A | T | 53 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(50): Show |
68 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-93-926A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125196 | |||||||
| chr14:92125499 | A | G | 2 | a0001c0001t0004g0099 a0001c0001t0100g0235 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-93-623A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125499 | |||||||
| chr14:92125634 | C | G | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
89 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-93-488C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125634 | |||||||
| chr14:92125823 | A | G | 1 | a0001c0001t0004g0099 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-93-299A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125823 | |||||||
| chr14:92125868 | T | C | 1 | a0001c0001t0004g0051 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-93-254T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125868 | |||||||
| chr14:92125925 | TTA | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-195_-93-194del others(2): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr14 | 92125925 | ||||||
| chr14:92125966 | A | G | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-93-156A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125966 | |||||||
| chr14:92125987 | T | G | 3 | a0001c0001t0114g0246 a0001c0001t0115g0247 a0001c0001t0122g0248 |
3 | HG01884.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-93-135T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92125987 | |||||||
| chr14:92126033 | C | G | 1 | a0001c0001t0097g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-93-89C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92126033 | |||||||
| chr14:92126047 | A | G | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-93-75A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 1/15 | chr14 | 92126047 | |||||||
| chr14:92126312 | A | G | 1 | a0001c0001t0097g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-35+132A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126312 | |||||||
| chr14:92126414 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
162 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-35+234A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126414 | |||||||
| chr14:92126598 | C | T | 6 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(3): Show |
6 | HG01255.hp2 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35+418C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126598 | |||||||
| chr14:92126673 | C | T | 1 | a0001c0001t0120g0252 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-35+493C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126673 | |||||||
| chr14:92126679 | C | T | 2 | a0001c0001t0090g0173 a0001c0001t0166g0098 |
2 | HG01168.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-35+499C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126679 | |||||||
| chr14:92126811 | A | G | 5 | a0001c0001t0025g0038 a0001c0001t0025g0171 a0001c0001t0025g0172 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+631A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92126811 | |||||||
| chr14:92127142 | A | T | 1 | a0001c0001t0080g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-35+962A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127142 | |||||||
| chr14:92127301 | A | G | 1 | a0001c0001t0008g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-35+1121A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127301 | |||||||
| chr14:92127437 | C | T | 1 | a0001c0001t0084g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-35+1257C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127437 | |||||||
| chr14:92127449 | T | G | 1 | a0001c0001t0033g0112 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-35+1269T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127449 | |||||||
| chr14:92127525 | A | G | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-35+1345A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127525 | |||||||
| chr14:92127526 | T | C | 1 | a0001c0001t0123g0186 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-35+1346T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127526 | |||||||
| chr14:92127666 | A | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35+1486A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127666 | |||||||
| chr14:92127869 | T | A | 1 | a0001c0001t0011g0236 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-35+1689T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127869 | |||||||
| chr14:92127993 | C | T | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.-35+1813C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92127993 | |||||||
| chr14:92128036 | C | G | 10 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0094 others(7): Show |
10 | HG02083.hp1 NA18952.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35+1856C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128036 | |||||||
| chr14:92128040 | C | T | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-35+1860C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128040 | |||||||
| chr14:92128235 | C | CA | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-35+2065dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr14 | 92128235 | ||||||
| chr14:92128343 | C | T | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-35+2163C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128343 | |||||||
| chr14:92128541 | T | C | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-35+2361T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128541 | |||||||
| chr14:92128900 | A | G | 2 | a0001c0001t0029g0135 a0001c0001t0141g0134 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-34-2051A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128900 | |||||||
| chr14:92128935 | G | T | 1 | a0001c0001t0002g0049 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-34-2016G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128935 | |||||||
| chr14:92128954 | A | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG00544.hp2 NA18612.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-34-1997A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128954 | |||||||
| chr14:92128961 | A | G | 1 | a0001c0001t0082g0177 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-34-1990A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92128961 | |||||||
| chr14:92129059 | A | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-1892A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129059 | |||||||
| chr14:92129060 | T | A | 1 | a0001c0001t0142g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-34-1891T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129060 | |||||||
| chr14:92129135 | G | A | 6 | a0001c0001t0006g0008 a0001c0001t0016g0188 a0001c0001t0017g0008 others(3): Show |
8 | HG02615.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34-1816G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129135 | |||||||
| chr14:92129137 | A | T | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-34-1814A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129137 | |||||||
| chr14:92129533 | T | G | 1 | a0001c0001t0133g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-34-1418T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129533 | |||||||
| chr14:92129543 | C | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-1408C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129543 | |||||||
| chr14:92129550 | C | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-1401C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129550 | |||||||
| chr14:92129555 | C | T | 1 | a0001c0001t0006g0211 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-34-1396C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129555 | |||||||
| chr14:92129567 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
9 | NA18951.hp1 NA18960.hp2 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34-1384T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129567 | |||||||
| chr14:92129649 | T | C | 1 | a0001c0001t0063g0113 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-34-1302T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129649 | |||||||
| chr14:92129660 | C | T | 10 | a0001c0001t0003g0050 a0001c0001t0004g0015 a0001c0001t0004g0029 others(7): Show |
11 | HG00558.hp1 HG00609.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34-1291C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129660 | |||||||
| chr14:92129809 | G | A | 1 | a0001c0001t0008g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-34-1142G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129809 | |||||||
| chr14:92129813 | T | C | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-34-1138T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129813 | |||||||
| chr14:92129917 | T | C | 1 | a0001c0001t0009g0144 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-34-1034T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92129917 | |||||||
| chr14:92130129 | C | T | 6 | a0001c0001t0116g0024 a0001c0001t0117g0024 a0001c0001t0118g0253 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34-822C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130129 | |||||||
| chr14:92130130 | G | A | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-821G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130130 | |||||||
| chr14:92130223 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-34-728C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130223 | |||||||
| chr14:92130465 | A | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
73 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-34-486A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130465 | |||||||
| chr14:92130532 | T | C | 3 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0121g0249 |
3 | HG02145.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-34-419T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130532 | |||||||
| chr14:92130548 | A | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34-403A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130548 | |||||||
| chr14:92130678 | G | A | 1 | a0001c0001t0003g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-34-273G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130678 | |||||||
| chr14:92130748 | A | T | 2 | a0001c0001t0030g0231 a0001c0001t0030g0232 |
2 | HG01069.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-34-203A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130748 | |||||||
| chr14:92130806 | A | G | 1 | a0001c0001t0013g0210 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-34-145A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130806 | |||||||
| chr14:92130884 | C | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
162 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-34-67C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130884 | |||||||
| chr14:92130885 | A | C | 1 | a0001c0001t0001g0163 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-34-66A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 2/15 | chr14 | 92130885 | |||||||
| chr14:92131203 | C | T | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149+70C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131203 | |||||||
| chr14:92131246 | G | A | 1 | a0001c0001t0138g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.149+113G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131246 | |||||||
| chr14:92131548 | T | C | 1 | a0001c0001t0008g0150 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.149+415T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131548 | |||||||
| chr14:92131695 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0162 a0001c0001t0024g0017 others(1): Show |
4 | NA18972.hp2 NA18995.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+562C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131695 | |||||||
| chr14:92131811 | C | T | 2 | a0001c0001t0003g0028 a0001c0001t0047g0028 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.149+678C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131811 | |||||||
| chr14:92131847 | AT | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0074 a0001c0001t0049g0027 others(2): Show |
5 | HG01069.hp1 NA18747.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+715delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131847 | |||||||
| chr14:92131848 | T | A | 90 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(87): Show |
91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.149+715T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131848 | |||||||
| chr14:92131851 | G | A | 93 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(90): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.149+718G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131851 | |||||||
| chr14:92131853 | T | A | 1 | a0001c0001t0150g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.149+720T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131853 | |||||||
| chr14:92131915 | A | G | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.149+782A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131915 | |||||||
| chr14:92131955 | C | A | 1 | a0001c0001t0097g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.149+822C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131955 | |||||||
| chr14:92131977 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.149+844T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92131977 | |||||||
| chr14:92132065 | C | T | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.149+932C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132065 | |||||||
| chr14:92132280 | A | G | 1 | a0001c0001t0129g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.149+1147A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132280 | |||||||
| chr14:92132291 | G | T | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.149+1158G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132291 | |||||||
| chr14:92132469 | G | C | 1 | a0001c0001t0067g0114 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.149+1336G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132469 | |||||||
| chr14:92132517 | A | G | 1 | a0001c0001t0037g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.149+1384A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132517 | |||||||
| chr14:92132526 | C | T | 31 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(28): Show |
36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.149+1393C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132526 | |||||||
| chr14:92132543 | G | A | 1 | a0001c0001t0124g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.149+1410G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132543 | |||||||
| chr14:92132569 | C | T | 1 | a0001c0001t0125g0185 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.149+1436C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132569 | |||||||
| chr14:92132621 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.150-1390G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132621 | |||||||
| chr14:92132703 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.150-1308C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132703 | |||||||
| chr14:92132767 | C | T | 1 | a0001c0001t0008g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.150-1244C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132767 | |||||||
| chr14:92132791 | A | C | 1 | a0001c0001t0076g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.150-1220A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92132791 | |||||||
| chr14:92133029 | G | A | 31 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(28): Show |
36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.150-982G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133029 | |||||||
| chr14:92133076 | C | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-935C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133076 | |||||||
| chr14:92133137 | T | C | 275 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(272): Show |
314 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.150-874T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133137 | |||||||
| chr14:92133139 | G | T | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.150-872G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133139 | |||||||
| chr14:92133144 | G | A | 1 | a0001c0001t0046g0106 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.150-867G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133144 | |||||||
| chr14:92133180 | G | A | 1 | a0001c0001t0146g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.150-831G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133180 | |||||||
| chr14:92133186 | G | A | 5 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0058 others(2): Show |
5 | NA18954.hp1 NA18966.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-825G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133186 | |||||||
| chr14:92133220 | GACCACCC others(15): Show |
G | 1 | a0001c0001t0066g0110 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.150-789_150-768del others(22): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 92133220 | ||||||
| chr14:92133235 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.150-776C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133235 | |||||||
| chr14:92133267 | A | G | 1 | a0001c0001t0010g0109 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.150-744A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133267 | |||||||
| chr14:92133291 | T | C | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-720T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133291 | |||||||
| chr14:92133343 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.150-668T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133343 | |||||||
| chr14:92133361 | G | A | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-650G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133361 | |||||||
| chr14:92133442 | T | TGTG | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.150-568_150-566dup others(3): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 92133442 | ||||||
| chr14:92133517 | A | G | 94 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(91): Show |
97 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.150-494A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133517 | |||||||
| chr14:92133529 | T | C | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.150-482T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133529 | |||||||
| chr14:92133622 | C | CT | 100 | a0001c0001t0001g0142 a0001c0001t0001g0178 a0001c0001t0003g0007 others(97): Show |
103 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.150-375dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr14 | 92133622 | ||||||
| chr14:92133646 | A | G | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.150-365A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133646 | |||||||
| chr14:92133652 | A | G | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.150-359A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133652 | |||||||
| chr14:92133833 | G | A | 5 | a0001c0001t0002g0043 a0001c0001t0002g0214 a0001c0001t0002g0215 others(2): Show |
5 | HG00099.hp2 HG00738.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-178G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 3/15 | chr14 | 92133833 | |||||||
| chr14:92134212 | G | A | 2 | a0001c0001t0026g0145 a0001c0001t0026g0146 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.310-38G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 4/15 | chr14 | 92134212 | |||||||
| chr14:92134441 | A | G | 56 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(53): Show |
71 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.415+86A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134441 | |||||||
| chr14:92134454 | G | T | 143 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(140): Show |
151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.415+99G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134454 | |||||||
| chr14:92134563 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.415+208G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134563 | |||||||
| chr14:92134614 | A | G | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.415+259A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134614 | |||||||
| chr14:92134674 | A | T | 2 | a0001c0001t0053g0207 a0001c0001t0054g0208 |
2 | HG00558.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.415+319A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134674 | |||||||
| chr14:92134761 | G | A | 1 | a0001c0001t0013g0181 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.415+406G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134761 | |||||||
| chr14:92134837 | A | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+482A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134837 | |||||||
| chr14:92134862 | C | G | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.416-505C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134862 | |||||||
| chr14:92134942 | A | C | 1 | a0001c0001t0004g0133 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.416-425A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92134942 | |||||||
| chr14:92135050 | A | G | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-317A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 5/15 | chr14 | 92135050 | |||||||
| chr14:92135536 | GTAT | G | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.545+45_545+47delAT others(1): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 92135536 | ||||||
| chr14:92135625 | G | A | 1 | a0001c0001t0090g0173 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.545+129G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92135625 | |||||||
| chr14:92135730 | G | A | 3 | a0001c0001t0026g0145 a0001c0001t0026g0146 a0001c0001t0093g0147 |
3 | HG02486.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.545+234G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92135730 | |||||||
| chr14:92135884 | T | C | 1 | a0001c0001t0084g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.545+388T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92135884 | |||||||
| chr14:92135885 | A | G | 143 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(140): Show |
151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.545+389A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92135885 | |||||||
| chr14:92136182 | G | A | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.545+686G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136182 | |||||||
| chr14:92136543 | T | C | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.545+1047T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136543 | |||||||
| chr14:92136618 | G | A | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.545+1122G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136618 | |||||||
| chr14:92136630 | A | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.545+1134A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136630 | |||||||
| chr14:92136753 | G | A | 2 | a0001c0001t0045g0191 a0001c0001t0045g0192 |
2 | HG01346.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.545+1257G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136753 | |||||||
| chr14:92136883 | T | C | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.546-1349T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136883 | |||||||
| chr14:92136931 | T | A | 1 | a0001c0001t0090g0173 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.546-1301T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136931 | |||||||
| chr14:92136967 | T | G | 322 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(319): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.546-1265T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92136967 | |||||||
| chr14:92137020 | T | TA | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.546-1201dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 92137020 | ||||||
| chr14:92137050 | TGCA | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-1178_546-1176d others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr14 | 92137050 | ||||||
| chr14:92137122 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.546-1110G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137122 | |||||||
| chr14:92137232 | T | C | 1 | a0001c0001t0118g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.546-1000T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137232 | |||||||
| chr14:92137294 | C | T | 31 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(28): Show |
36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.546-938C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137294 | |||||||
| chr14:92137320 | C | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-912C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137320 | |||||||
| chr14:92137919 | G | C | 1 | a0001c0001t0063g0113 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.546-313G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92137919 | |||||||
| chr14:92138138 | T | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-94T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 6/15 | chr14 | 92138138 | |||||||
| chr14:92138361 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
7 | HG00544.hp2 HG02135.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+14C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92138361 | |||||||
| chr14:92138580 | C | A | 1 | a0001c0001t0118g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.661+233C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92138580 | |||||||
| chr14:92138799 | A | G | 31 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(28): Show |
36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.661+452A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92138799 | |||||||
| chr14:92138897 | T | TG | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.661+552dupG | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92138897 | ||||||
| chr14:92138950 | C | T | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.661+603C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92138950 | |||||||
| chr14:92139037 | C | T | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.661+690C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139037 | |||||||
| chr14:92139056 | C | T | 1 | a0001c0001t0048g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.661+709C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139056 | |||||||
| chr14:92139095 | G | A | 1 | a0001c0001t0047g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.661+748G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139095 | |||||||
| chr14:92139169 | C | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.661+822C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139169 | |||||||
| chr14:92139234 | G | A | 3 | a0001c0001t0003g0254 a0001c0001t0019g0107 a0001c0001t0046g0106 |
3 | HG02683.hp1 HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.661+887G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139234 | |||||||
| chr14:92139244 | C | T | 1 | a0001c0001t0013g0206 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.661+897C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139244 | |||||||
| chr14:92139342 | G | A | 1 | a0001c0001t0124g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.661+995G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139342 | |||||||
| chr14:92139403 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
277 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.661+1056T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139403 | |||||||
| chr14:92139411 | C | T | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.661+1064C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139411 | |||||||
| chr14:92139463 | C | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.661+1116C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139463 | |||||||
| chr14:92139465 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.661+1118G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139465 | |||||||
| chr14:92139534 | A | G | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.661+1187A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139534 | |||||||
| chr14:92139539 | C | CT | 18 | a0001c0001t0001g0162 a0001c0001t0003g0056 a0001c0001t0006g0205 others(15): Show |
20 | HG00140.hp2 HG00408.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.661+1209dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139539 | ||||||
| chr14:92139539 | CT | C | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.661+1209delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139539 | ||||||
| chr14:92139592 | G | A | 1 | a0001c0001t0013g0206 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.661+1245G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139592 | |||||||
| chr14:92139735 | C | T | 34 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(31): Show |
39 | HG00408.hp2 HG01884.hp1 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.661+1388C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139735 | |||||||
| chr14:92139741 | G | A | 94 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(91): Show |
97 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.661+1394G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139741 | |||||||
| chr14:92139786 | G | A | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.661+1439G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139786 | |||||||
| chr14:92139787 | C | A | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.661+1440C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139787 | |||||||
| chr14:92139821 | A | G | 1 | a0001c0001t0019g0086 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.661+1474A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139821 | |||||||
| chr14:92139846 | C | A | 1 | a0001c0001t0002g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.661+1499C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139846 | |||||||
| chr14:92139948 | C | CT | 8 | a0001c0001t0012g0020 a0001c0001t0012g0125 a0001c0001t0013g0182 others(5): Show |
9 | HG01975.hp1 HG02055.hp2 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.661+1602dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139948 | ||||||
| chr14:92139949 | TA | T | 3 | a0001c0001t0005g0042 a0001c0001t0013g0042 a0001c0001t0131g0183 |
3 | HG03942.hp1 NA18959.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.661+1603delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139949 | |||||||
| chr14:92139950 | A | AT | 97 | a0001c0001t0001g0142 a0001c0001t0001g0175 a0001c0001t0002g0001 others(94): Show |
102 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.661+1625dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139950 | ||||||
| chr14:92139950 | A | ATT | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
122 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.661+1624_661+1625d others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139950 | ||||||
| chr14:92139950 | A | ATTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0178 a0001c0001t0001g0179 others(5): Show |
8 | HG02145.hp2 HG02683.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+1623_661+1625d others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92139950 | ||||||
| chr14:92139950 | A | T | 54 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(51): Show |
69 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.661+1603A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92139950 | |||||||
| chr14:92140042 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.661+1695C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140042 | |||||||
| chr14:92140103 | G | T | 1 | a0001c0001t0002g0215 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.661+1756G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140103 | |||||||
| chr14:92140143 | G | T | 4 | a0001c0001t0026g0145 a0001c0001t0026g0146 a0001c0001t0026g0148 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+1796G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140143 | |||||||
| chr14:92140193 | C | G | 3 | a0001c0001t0014g0240 a0001c0001t0014g0241 a0001c0001t0014g0242 |
3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.661+1846C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140193 | |||||||
| chr14:92140194 | C | T | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.661+1847C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140194 | |||||||
| chr14:92140241 | C | T | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.661+1894C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140241 | |||||||
| chr14:92140399 | A | G | 1 | a0001c0001t0027g0227 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.662-1765A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140399 | |||||||
| chr14:92140424 | A | AC | 5 | a0001c0001t0015g0048 a0001c0001t0041g0048 a0001c0001t0107g0226 others(2): Show |
5 | HG02055.hp2 HG03239.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-1735dupC | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92140424 | ||||||
| chr14:92140434 | C | CT | 181 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(178): Show |
204 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.662-1713dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92140434 | ||||||
| chr14:92140434 | C | CTT | 11 | a0001c0001t0006g0205 a0001c0001t0042g0244 a0001c0001t0042g0250 others(8): Show |
11 | HG00438.hp2 HG02145.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.662-1714_662-1713d others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92140434 | ||||||
| chr14:92140494 | G | A | 1 | a0001c0001t0112g0225 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.662-1670G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140494 | |||||||
| chr14:92140530 | T | C | 31 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(28): Show |
36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.662-1634T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140530 | |||||||
| chr14:92140557 | C | T | 4 | a0001c0001t0026g0145 a0001c0001t0026g0146 a0001c0001t0026g0148 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1607C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140557 | |||||||
| chr14:92140654 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
67 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.662-1510G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140654 | |||||||
| chr14:92140657 | C | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-1507C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140657 | |||||||
| chr14:92140686 | C | A | 1 | a0001c0001t0002g0214 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.662-1478C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140686 | |||||||
| chr14:92140703 | A | AT | 94 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(91): Show |
97 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.662-1459dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr14 | 92140703 | ||||||
| chr14:92140747 | A | G | 1 | a0001c0001t0102g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.662-1417A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140747 | |||||||
| chr14:92140806 | T | A | 1 | a0001c0001t0077g0151 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.662-1358T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140806 | |||||||
| chr14:92140941 | A | G | 1 | a0001c0001t0009g0138 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.662-1223A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92140941 | |||||||
| chr14:92141040 | A | G | 1 | a0001c0001t0028g0223 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.662-1124A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141040 | |||||||
| chr14:92141086 | A | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-1078A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141086 | |||||||
| chr14:92141230 | A | T | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.662-934A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141230 | |||||||
| chr14:92141488 | C | T | 1 | a0001c0001t0005g0195 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.662-676C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141488 | |||||||
| chr14:92141522 | C | T | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.662-642C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92141522 | |||||||
| chr14:92142052 | G | A | 1 | a0001c0001t0004g0059 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.662-112G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92142052 | |||||||
| chr14:92142135 | T | C | 1 | a0001c0001t0010g0092 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.662-29T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 7/15 | chr14 | 92142135 | |||||||
| chr14:92142563 | C | G | 31 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(28): Show |
36 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(33): Show |
intron_variant | MODIFIER | c.849+212C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 8/15 | chr14 | 92142563 | |||||||
| chr14:92142577 | T | A | 1 | a0001c0001t0027g0228 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.849+226T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 8/15 | chr14 | 92142577 | |||||||
| chr14:92142990 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.850-14T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 8/15 | chr14 | 92142990 | |||||||
| chr14:92143358 | A | G | 1 | a0001c0001t0094g0239 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1140+64A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143358 | |||||||
| chr14:92143486 | C | A | 1 | a0001c0001t0006g0211 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1140+192C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143486 | |||||||
| chr14:92143486 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1140+192C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143486 | |||||||
| chr14:92143544 | T | TA | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+259dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92143544 | ||||||
| chr14:92143665 | G | T | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+371G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143665 | |||||||
| chr14:92143766 | TG | T | 62 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(59): Show |
77 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1140+474delG | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92143766 | ||||||
| chr14:92143799 | CGTT | C | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+508_1140+510d others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92143799 | ||||||
| chr14:92143869 | T | C | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+575T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143869 | |||||||
| chr14:92143879 | C | G | 1 | a0001c0001t0014g0241 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1140+585C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143879 | |||||||
| chr14:92143987 | C | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+693C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92143987 | |||||||
| chr14:92144044 | G | A | 1 | a0001c0001t0018g0060 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1140+750G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144044 | |||||||
| chr14:92144082 | T | C | 5 | a0001c0001t0003g0254 a0001c0001t0010g0109 a0001c0001t0019g0107 others(2): Show |
5 | HG01081.hp1 HG02683.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+788T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144082 | |||||||
| chr14:92144086 | C | T | 1 | a0001c0001t0146g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1140+792C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144086 | |||||||
| chr14:92144259 | T | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
162 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1140+965T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144259 | |||||||
| chr14:92144598 | T | G | 1 | a0001c0001t0008g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1140+1304T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144598 | |||||||
| chr14:92144717 | A | G | 4 | a0001c0001t0002g0022 a0001c0001t0002g0222 a0001c0001t0028g0223 others(1): Show |
6 | HG01081.hp2 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1140+1423A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144717 | |||||||
| chr14:92144732 | C | A | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1140+1438C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144732 | |||||||
| chr14:92144742 | G | C | 1 | a0001c0001t0010g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1140+1448G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144742 | |||||||
| chr14:92144887 | A | G | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+1593A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92144887 | |||||||
| chr14:92145136 | A | T | 32 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(29): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1140+1842A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145136 | |||||||
| chr14:92145144 | T | G | 6 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(3): Show |
6 | HG01255.hp2 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1140+1850T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145144 | |||||||
| chr14:92145290 | G | A | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1140+1996G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145290 | |||||||
| chr14:92145346 | A | C | 62 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(59): Show |
77 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1140+2052A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145346 | |||||||
| chr14:92145346 | A | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1140+2052A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145346 | |||||||
| chr14:92145355 | T | TA | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+2063dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92145355 | ||||||
| chr14:92145626 | A | G | 1 | a0001c0001t0016g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1140+2332A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145626 | |||||||
| chr14:92145655 | C | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
162 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1140+2361C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145655 | |||||||
| chr14:92145738 | A | C | 1 | a0001c0001t0166g0098 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1140+2444A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145738 | |||||||
| chr14:92145870 | C | G | 1 | a0001c0001t0094g0239 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1140+2576C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145870 | |||||||
| chr14:92145969 | T | A | 1 | a0001c0001t0002g0021 | 3 | HG01168.hp1 HG01169.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1140+2675T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92145969 | |||||||
| chr14:92146093 | A | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+2799A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146093 | |||||||
| chr14:92146099 | A | AT | 5 | a0001c0001t0003g0031 a0001c0001t0003g0096 a0001c0001t0010g0095 others(2): Show |
5 | NA18952.hp2 NA18960.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+2805_1140+280 others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146099 | |||||||
| chr14:92146194 | G | T | 1 | a0001c0001t0047g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1140+2900G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146194 | |||||||
| chr14:92146296 | C | T | 1 | a0001c0001t0139g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1140+3002C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146296 | |||||||
| chr14:92146303 | C | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+3009C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146303 | |||||||
| chr14:92146387 | G | C | 1 | a0001c0001t0151g0062 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1140+3093G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146387 | |||||||
| chr14:92146503 | A | G | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1140+3209A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146503 | |||||||
| chr14:92146523 | AAAAC | A | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+3237_1140+324 others(8): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92146523 | ||||||
| chr14:92146554 | C | G | 1 | a0001c0001t0040g0036 | 2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1140+3260C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146554 | |||||||
| chr14:92146720 | C | CTT | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+3427_1140+342 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92146720 | ||||||
| chr14:92146854 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(63): Show |
80 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1140+3560C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146854 | |||||||
| chr14:92146957 | C | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0141 a0001c0001t0001g0157 others(2): Show |
7 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.1140+3663C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92146957 | |||||||
| chr14:92146990 | AC | A | 32 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(29): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1140+3698delC | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92146990 | ||||||
| chr14:92147219 | G | C | 1 | a0001c0001t0034g0101 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1140+3925G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147219 | |||||||
| chr14:92147254 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0101g0009 |
5 | HG03490.hp2 HG03492.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+3960A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147254 | |||||||
| chr14:92147409 | T | C | 32 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(29): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1140+4115T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147409 | |||||||
| chr14:92147630 | A | C | 92 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(89): Show |
95 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1140+4336A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147630 | |||||||
| chr14:92147860 | A | G | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1140+4566A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147860 | |||||||
| chr14:92147894 | A | T | 1 | a0001c0001t0002g0216 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1140+4600A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147894 | |||||||
| chr14:92147902 | A | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
312 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.1140+4608A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147902 | |||||||
| chr14:92147958 | C | T | 3 | a0001c0001t0099g0220 a0001c0001t0100g0235 a0001c0001t0109g0234 |
3 | HG01175.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1140+4664C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147958 | |||||||
| chr14:92147980 | C | T | 1 | a0001c0001t0168g0083 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1140+4686C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92147980 | |||||||
| chr14:92148131 | C | G | 91 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(88): Show |
94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1140+4837C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148131 | |||||||
| chr14:92148178 | T | C | 1 | a0001c0001t0146g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1140+4884T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148178 | |||||||
| chr14:92148310 | T | G | 5 | a0001c0001t0026g0145 a0001c0001t0026g0146 a0001c0001t0026g0148 others(2): Show |
5 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1140+5016T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148310 | |||||||
| chr14:92148360 | G | C | 2 | a0001c0001t0068g0116 a0001c0001t0069g0115 |
2 | NA18946.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1140+5066G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148360 | |||||||
| chr14:92148397 | G | A | 142 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(139): Show |
150 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1140+5103G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148397 | |||||||
| chr14:92148483 | C | T | 3 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0121g0249 |
3 | HG02145.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1140+5189C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148483 | |||||||
| chr14:92148494 | A | G | 1 | a0001c0001t0006g0204 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1140+5200A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148494 | |||||||
| chr14:92148540 | A | G | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+5246A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148540 | |||||||
| chr14:92148664 | G | T | 2 | a0001c0001t0003g0028 a0001c0001t0047g0028 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1140+5370G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148664 | |||||||
| chr14:92148771 | C | CA | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+5493dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92148771 | ||||||
| chr14:92148771 | CA | C | 6 | a0001c0001t0001g0156 a0001c0001t0009g0140 a0001c0001t0025g0172 others(3): Show |
6 | HG02451.hp1 HG02965.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.1140+5493delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92148771 | ||||||
| chr14:92148797 | G | GTA | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1140+5515_1140+551 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92148797 | ||||||
| chr14:92148808 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1140+5514T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92148808 | |||||||
| chr14:92149031 | C | A | 143 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(140): Show |
151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1141-5327C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149031 | |||||||
| chr14:92149119 | T | TACTGGTA others(8): Show |
1 | a0001c0001t0060g0111 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1141-5238_1141-522 others(19): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92149119 | ||||||
| chr14:92149147 | C | T | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-5211C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149147 | |||||||
| chr14:92149155 | A | G | 1 | a0001c0001t0088g0155 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1141-5203A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149155 | |||||||
| chr14:92149213 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0008g0005 others(4): Show |
10 | NA18961.hp1 NA18965.hp1 NA18999.hp1 others(7): Show |
intron_variant | MODIFIER | c.1141-5145A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149213 | |||||||
| chr14:92149369 | G | A | 1 | a0001c0001t0129g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1141-4989G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149369 | |||||||
| chr14:92149397 | C | CAT | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1141-4960_1141-495 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92149397 | ||||||
| chr14:92149481 | C | T | 1 | a0001c0001t0006g0211 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1141-4877C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149481 | |||||||
| chr14:92149573 | G | T | 1 | a0001c0001t0004g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1141-4785G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149573 | |||||||
| chr14:92149665 | G | GT | 37 | a0001c0001t0016g0126 a0001c0001t0020g0011 a0001c0001t0021g0004 others(34): Show |
42 | HG00408.hp2 HG02040.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.1141-4684dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92149665 | ||||||
| chr14:92149725 | G | A | 1 | a0001c0001t0005g0194 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1141-4633G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149725 | |||||||
| chr14:92149741 | C | T | 2 | a0001c0001t0003g0094 a0001c0001t0113g0245 |
2 | HG02809.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1141-4617C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149741 | |||||||
| chr14:92149742 | G | A | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-4616G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149742 | |||||||
| chr14:92149817 | G | A | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1141-4541G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149817 | |||||||
| chr14:92149821 | G | A | 200 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(197): Show |
223 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1141-4537G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149821 | |||||||
| chr14:92149858 | T | C | 32 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(29): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1141-4500T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149858 | |||||||
| chr14:92149947 | G | A | 1 | a0001c0001t0053g0207 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1141-4411G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92149947 | |||||||
| chr14:92150112 | T | C | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-4246T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150112 | |||||||
| chr14:92150126 | A | ATT | 273 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
312 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.1141-4223_1141-422 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92150126 | ||||||
| chr14:92150179 | C | T | 143 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(140): Show |
151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1141-4179C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150179 | |||||||
| chr14:92150193 | C | T | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-4165C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150193 | |||||||
| chr14:92150414 | A | T | 1 | a0001c0001t0025g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1141-3944A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150414 | |||||||
| chr14:92150415 | C | A | 1 | a0001c0001t0025g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1141-3943C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150415 | |||||||
| chr14:92150427 | T | TTG | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-3921_1141-392 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92150427 | ||||||
| chr14:92150437 | G | T | 1 | a0001c0001t0128g0203 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1141-3921G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150437 | |||||||
| chr14:92150438 | T | TG | 4 | a0001c0001t0026g0145 a0001c0001t0026g0146 a0001c0001t0026g0148 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-3920_1141-391 others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150438 | |||||||
| chr14:92150439 | T | G | 1 | a0001c0001t0100g0235 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1141-3919T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150439 | |||||||
| chr14:92150622 | C | G | 1 | a0001c0001t0013g0206 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1141-3736C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150622 | |||||||
| chr14:92150700 | A | G | 1 | a0001c0001t0010g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1141-3658A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92150700 | |||||||
| chr14:92151002 | A | G | 1 | a0001c0001t0010g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1141-3356A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151002 | |||||||
| chr14:92151436 | TA | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0008g0005 others(48): Show |
60 | HG00408.hp2 HG01069.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.1141-2907delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92151436 | ||||||
| chr14:92151437 | A | T | 58 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(55): Show |
73 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1141-2921A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151437 | |||||||
| chr14:92151438 | A | T | 2 | a0001c0001t0013g0182 a0001c0001t0124g0237 |
2 | HG02055.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1141-2920A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151438 | |||||||
| chr14:92151451 | A | T | 90 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(87): Show |
93 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1141-2907A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151451 | |||||||
| chr14:92151452 | TTAACAC | T | 90 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(87): Show |
93 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1141-2905_1141-290 others(10): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151452 | |||||||
| chr14:92151453 | T | C | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-2905T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151453 | |||||||
| chr14:92151455 | A | C | 7 | a0001c0001t0002g0021 a0001c0001t0002g0043 a0001c0001t0002g0214 others(4): Show |
9 | HG00099.hp2 HG00642.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1141-2903A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151455 | |||||||
| chr14:92151669 | G | C | 1 | a0001c0001t0160g0065 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1141-2689G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151669 | |||||||
| chr14:92151866 | G | A | 3 | a0001c0001t0014g0240 a0001c0001t0014g0241 a0001c0001t0014g0242 |
3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1141-2492G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151866 | |||||||
| chr14:92151925 | T | G | 137 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(134): Show |
145 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1141-2433T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92151925 | |||||||
| chr14:92152010 | CA | C | 60 | a0001c0001t0001g0178 a0001c0001t0002g0001 a0001c0001t0002g0009 others(57): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1141-2331delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152010 | ||||||
| chr14:92152010 | CAA | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
208 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1141-2332_1141-233 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152010 | ||||||
| chr14:92152010 | CAAA | C | 89 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(86): Show |
92 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1141-2333_1141-233 others(7): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152010 | ||||||
| chr14:92152035 | C | T | 1 | a0001c0001t0011g0046 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1141-2323C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152035 | |||||||
| chr14:92152159 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1141-2199C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152159 | |||||||
| chr14:92152215 | C | T | 1 | a0001c0001t0134g0201 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1141-2143C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152215 | |||||||
| chr14:92152237 | C | T | 1 | a0001c0001t0052g0040 | 2 | HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1141-2121C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152237 | |||||||
| chr14:92152271 | A | C | 1 | a0001c0001t0008g0154 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1141-2087A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152271 | |||||||
| chr14:92152337 | C | T | 1 | a0001c0001t0010g0081 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1141-2021C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152337 | |||||||
| chr14:92152381 | G | A | 1 | a0001c0001t0008g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1141-1977G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152381 | |||||||
| chr14:92152424 | C | T | 1 | a0001c0001t0134g0201 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1141-1934C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152424 | |||||||
| chr14:92152455 | T | C | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1141-1903T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152455 | |||||||
| chr14:92152651 | C | T | 92 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(89): Show |
95 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1141-1707C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152651 | |||||||
| chr14:92152659 | G | T | 1 | a0001c0001t0004g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1141-1699G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152659 | |||||||
| chr14:92152821 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1141-1537T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92152821 | |||||||
| chr14:92152991 | C | CT | 58 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(55): Show |
73 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1141-1358dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152991 | ||||||
| chr14:92152991 | CTT | C | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-1359_1141-135 others(6): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92152991 | ||||||
| chr14:92153051 | G | T | 32 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(29): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.1141-1307G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153051 | |||||||
| chr14:92153058 | A | G | 1 | a0001c0001t0046g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1141-1300A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153058 | |||||||
| chr14:92153061 | T | TCAAATTT others(2603): Show |
2 | a0001c0001t0114g0246 a0001c0001t0115g0247 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2614): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2603): Show |
1 | a0001c0001t0122g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2614): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2608): Show |
2 | a0001c0001t0033g0034 a0001c0001t0070g0034 |
2 | HG02523.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2619): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2608): Show |
20 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0031g0004 others(17): Show |
24 | HG02040.hp2 HG02165.hp1 HG03491.hp1 others(21): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2619): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2609): Show |
1 | a0001c0001t0060g0111 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2620): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2609): Show |
2 | a0001c0001t0034g0033 a0001c0001t0036g0033 |
2 | NA18950.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2620): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2611): Show |
1 | a0001c0001t0064g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2622): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2610): Show |
1 | a0001c0001t0021g0121 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2621): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2609): Show |
1 | a0001c0001t0021g0122 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2620): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2609): Show |
2 | a0001c0001t0032g0035 a0001c0001t0066g0110 |
3 | NA18989.hp1 NA18997.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2620): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2621): Show |
1 | a0001c0001t0056g0123 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2632): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2627): Show |
1 | a0001c0001t0062g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2638): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2482): Show |
1 | a0001c0001t0003g0068 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2493): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2613): Show |
1 | a0001c0001t0166g0098 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
1 | a0001c0001t0004g0099 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2613): Show |
2 | a0001c0001t0003g0028 a0001c0001t0047g0028 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2483): Show |
2 | a0001c0001t0140g0025 a0001c0001t0153g0025 |
2 | HG02165.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2494): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2483): Show |
1 | a0001c0001t0004g0059 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2494): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2484): Show |
1 | a0001c0001t0019g0086 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2495): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
1 | a0001c0001t0004g0069 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
26 | a0001c0001t0003g0007 a0001c0001t0003g0030 a0001c0001t0003g0031 others(23): Show |
28 | HG00423.hp2 HG01258.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
2 | a0001c0001t0003g0094 a0001c0001t0019g0093 |
2 | NA19085.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2613): Show |
1 | a0001c0001t0003g0057 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2615): Show |
1 | a0001c0001t0046g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2616): Show |
1 | a0001c0001t0003g0056 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
1 | a0001c0001t0019g0107 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
1 | a0001c0001t0146g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
1 | a0001c0001t0029g0135 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2615): Show |
1 | a0001c0001t0004g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2615): Show |
1 | a0001c0001t0004g0071 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2615): Show |
3 | a0001c0001t0003g0053 a0001c0001t0018g0072 a0001c0001t0154g0088 |
3 | NA18961.hp2 NA18988.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2616): Show |
1 | a0001c0001t0019g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2617): Show |
1 | a0001c0001t0004g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2617): Show |
1 | a0001c0001t0003g0096 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2616): Show |
1 | a0001c0001t0158g0067 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2484): Show |
5 | a0001c0001t0003g0010 a0001c0001t0004g0010 a0001c0001t0010g0010 others(2): Show |
5 | HG01074.hp2 HG01934.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2495): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2615): Show |
1 | a0001c0001t0148g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2615): Show |
2 | a0001c0001t0003g0074 a0001c0001t0150g0054 |
2 | NA18941.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2615): Show |
12 | a0001c0001t0003g0026 a0001c0001t0003g0103 a0001c0001t0004g0026 others(9): Show |
12 | HG00438.hp2 HG00558.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2616): Show |
1 | a0001c0001t0155g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2617): Show |
1 | a0001c0001t0018g0077 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2618): Show |
1 | a0001c0001t0048g0108 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2629): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2618): Show |
1 | a0001c0001t0139g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2629): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2617): Show |
1 | a0001c0001t0003g0104 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2615): Show |
1 | a0001c0001t0010g0109 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2616): Show |
4 | a0001c0001t0003g0064 a0001c0001t0004g0029 a0001c0001t0048g0132 others(1): Show |
4 | HG03209.hp2 NA18949.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2619): Show |
1 | a0001c0001t0168g0083 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2630): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2621): Show |
1 | a0001c0001t0004g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2632): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2617): Show |
1 | a0001c0001t0004g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2628): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2618): Show |
1 | a0001c0001t0029g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2629): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
1 | a0001c0001t0050g0097 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2200): Show |
1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2211): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
1 | a0002c0002t0010g0080 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2616): Show |
1 | a0001c0001t0003g0058 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2627): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2611): Show |
1 | a0001c0001t0118g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2622): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2611): Show |
1 | a0001c0001t0165g0251 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2622): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2612): Show |
5 | a0001c0001t0042g0244 a0001c0001t0116g0024 a0001c0001t0117g0024 others(2): Show |
5 | HG02922.hp1 HG02970.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2623): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
1 | a0001c0001t0121g0249 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2613): Show |
1 | a0001c0001t0042g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2613): Show |
1 | a0001c0001t0010g0061 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2624): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2614): Show |
1 | a0001c0001t0049g0027 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1141-1282_1141-128 others(2625): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153061 | T | TCAAATTT others(2615): Show |
1 | a0001c0001t0010g0092 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1141-1282_1141-128 others(2626): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153061 | ||||||
| chr14:92153482 | T | C | 2 | a0001c0001t0129g0209 a0001c0001t0132g0196 |
2 | HG01167.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1141-876T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153482 | |||||||
| chr14:92153529 | A | G | 1 | a0001c0001t0145g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1141-829A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153529 | |||||||
| chr14:92153703 | C | CT | 129 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
160 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1141-639dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153703 | ||||||
| chr14:92153734 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.1141-624T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153734 | |||||||
| chr14:92153866 | C | CT | 22 | a0001c0001t0001g0162 a0001c0001t0001g0176 a0001c0001t0003g0056 others(19): Show |
22 | HG01884.hp1 HG01934.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.1141-472dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153866 | ||||||
| chr14:92153866 | C | CTTT | 29 | a0001c0001t0004g0082 a0001c0001t0020g0011 a0001c0001t0021g0004 others(26): Show |
34 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(31): Show |
intron_variant | MODIFIER | c.1141-474_1141-472d others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153866 | ||||||
| chr14:92153867 | T | G | 1 | a0001c0001t0102g0224 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1141-491T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153867 | |||||||
| chr14:92153886 | T | A | 1 | a0001c0001t0026g0145 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1141-472T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153886 | |||||||
| chr14:92153886 | T | TA | 4 | a0001c0001t0026g0146 a0001c0001t0026g0148 a0001c0001t0085g0149 others(1): Show |
4 | HG02486.hp2 HG03041.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-471dupA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr14 | 92153886 | ||||||
| chr14:92153907 | T | G | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1141-451T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92153907 | |||||||
| chr14:92154092 | A | G | 6 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(3): Show |
6 | HG01255.hp2 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1141-266A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92154092 | |||||||
| chr14:92154159 | A | T | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1141-199A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 9/15 | chr14 | 92154159 | |||||||
| chr14:92154480 | T | G | 2 | a0001c0001t0003g0128 a0001c0001t0004g0133 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1241+22T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154480 | |||||||
| chr14:92154566 | AT | A | 4 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0004g0051 others(1): Show |
4 | NA18954.hp1 NA18966.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241+112delT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr14 | 92154566 | ||||||
| chr14:92154710 | G | T | 8 | a0001c0001t0003g0128 a0001c0001t0004g0133 a0001c0001t0029g0130 others(5): Show |
8 | HG01891.hp1 HG02622.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241+252G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154710 | |||||||
| chr14:92154747 | A | G | 1 | a0001c0001t0004g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1241+289A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154747 | |||||||
| chr14:92154842 | A | G | 1 | a0001c0001t0109g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1242-281A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154842 | |||||||
| chr14:92154951 | T | C | 3 | a0001c0001t0014g0240 a0001c0001t0014g0241 a0001c0001t0014g0242 |
3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1242-172T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154951 | |||||||
| chr14:92154956 | G | A | 2 | a0001c0001t0068g0116 a0001c0001t0069g0115 |
2 | NA18946.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1242-167G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92154956 | |||||||
| chr14:92155033 | T | C | 1 | a0001c0001t0095g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1242-90T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 10/15 | chr14 | 92155033 | |||||||
| chr14:92155490 | A | G | 1 | a0001c0001t0142g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1442+167A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155490 | |||||||
| chr14:92155560 | G | A | 93 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(90): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1442+237G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155560 | |||||||
| chr14:92155584 | G | A | 3 | a0001c0001t0003g0128 a0001c0001t0004g0133 a0001c0001t0048g0132 |
3 | HG02970.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1442+261G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155584 | |||||||
| chr14:92155600 | T | A | 1 | a0001c0001t0151g0062 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1442+277T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155600 | |||||||
| chr14:92155770 | TA | T | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.1442+460delA | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr14 | 92155770 | ||||||
| chr14:92155806 | G | A | 1 | a0001c0001t0010g0109 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1442+483G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155806 | |||||||
| chr14:92155811 | T | A | 143 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(140): Show |
151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1442+488T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155811 | |||||||
| chr14:92155959 | A | G | 3 | a0001c0001t0005g0018 a0001c0001t0006g0018 a0001c0001t0013g0181 |
4 | NA18980.hp2 NA18986.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1443-520A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155959 | |||||||
| chr14:92155967 | A | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1443-512A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155967 | |||||||
| chr14:92155980 | G | A | 143 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(140): Show |
151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1443-499G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92155980 | |||||||
| chr14:92156021 | G | A | 1 | a0001c0001t0007g0044 | 2 | HG01433.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1443-458G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156021 | |||||||
| chr14:92156060 | C | T | 1 | a0001c0001t0124g0237 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1443-419C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156060 | |||||||
| chr14:92156107 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0110g0221 |
2 | HG01081.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1443-372G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156107 | |||||||
| chr14:92156167 | G | A | 1 | a0001c0001t0024g0152 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1443-312G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156167 | |||||||
| chr14:92156297 | C | A | 1 | a0001c0001t0013g0182 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1443-182C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156297 | |||||||
| chr14:92156335 | T | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1443-144T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156335 | |||||||
| chr14:92156343 | C | T | 1 | a0001c0001t0005g0200 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1443-136C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 11/15 | chr14 | 92156343 | |||||||
| chr14:92156711 | C | T | 1 | a0001c0001t0129g0209 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1595+80C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92156711 | |||||||
| chr14:92156754 | A | AAATTT | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.1595+125_1595+129d others(7): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 92156754 | ||||||
| chr14:92156953 | C | T | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1595+322C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92156953 | |||||||
| chr14:92157005 | A | G | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1595+374A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157005 | |||||||
| chr14:92157069 | C | A | 1 | a0001c0001t0009g0158 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1595+438C>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157069 | |||||||
| chr14:92157520 | C | T | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.1596-139C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157520 | |||||||
| chr14:92157521 | AAAAAT | A | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596-129_1596-125d others(7): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr14 | 92157521 | ||||||
| chr14:92157552 | CAT | C | 94 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(91): Show |
98 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1596-106_1596-105d others(4): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157552 | |||||||
| chr14:92157604 | A | T | 1 | a0001c0001t0026g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1596-55A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157604 | |||||||
| chr14:92157645 | A | G | 4 | a0001c0001t0005g0212 a0001c0001t0017g0019 a0001c0001t0043g0019 others(1): Show |
5 | HG02280.hp1 HG02451.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596-14A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 12/15 | chr14 | 92157645 | |||||||
| chr14:92157946 | GATAAC | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821+65_1821+69del others(5): Show |
CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr14 | 92157946 | ||||||
| chr14:92158018 | A | T | 2 | a0001c0001t0003g0028 a0001c0001t0047g0028 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1821+134A>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158018 | |||||||
| chr14:92158174 | T | G | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1821+290T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158174 | |||||||
| chr14:92158303 | C | T | 10 | a0001c0001t0005g0018 a0001c0001t0006g0014 a0001c0001t0006g0018 others(7): Show |
12 | HG00621.hp1 HG02015.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.1821+419C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158303 | |||||||
| chr14:92158305 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1821+421G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158305 | |||||||
| chr14:92158722 | C | T | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1822-261C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158722 | |||||||
| chr14:92158723 | G | A | 93 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(90): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1822-260G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158723 | |||||||
| chr14:92158843 | G | A | 1 | a0001c0001t0079g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1822-140G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158843 | |||||||
| chr14:92158964 | C | T | 12 | a0001c0001t0042g0244 a0001c0001t0042g0250 a0001c0001t0114g0246 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1822-19C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 13/15 | chr14 | 92158964 | |||||||
| chr14:92159427 | C | G | 1 | a0001c0001t0127g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2121+145C>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159427 | |||||||
| chr14:92159545 | G | A | 1 | a0001c0001t0044g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2121+263G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159545 | |||||||
| chr14:92159559 | A | G | 143 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(140): Show |
151 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.2121+277A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159559 | |||||||
| chr14:92159576 | G | C | 2 | a0001c0001t0002g0045 a0001c0001t0167g0045 |
2 | HG00323.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.2121+294G>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159576 | |||||||
| chr14:92159792 | A | G | 1 | a0001c0001t0168g0083 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2121+510A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159792 | |||||||
| chr14:92159929 | A | G | 2 | a0001c0001t0029g0131 a0001c0001t0148g0129 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2121+647A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159929 | |||||||
| chr14:92159933 | T | G | 2 | a0001c0001t0053g0207 a0001c0001t0054g0208 |
2 | HG00558.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2121+651T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159933 | |||||||
| chr14:92159942 | A | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2121+660A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159942 | |||||||
| chr14:92159953 | G | GT | 151 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(148): Show |
169 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.2121+681dupT | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr14 | 92159953 | ||||||
| chr14:92159994 | G | A | 93 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(90): Show |
96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2121+712G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92159994 | |||||||
| chr14:92160072 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.2121+790C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160072 | |||||||
| chr14:92160144 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2121+862G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160144 | |||||||
| chr14:92160151 | C | T | 1 | a0001c0001t0064g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2121+869C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160151 | |||||||
| chr14:92160194 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.2121+912C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160194 | |||||||
| chr14:92160250 | A | C | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.2122-862A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160250 | |||||||
| chr14:92160251 | A | G | 4 | a0001c0001t0014g0240 a0001c0001t0014g0241 a0001c0001t0014g0242 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-861A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160251 | |||||||
| chr14:92160436 | A | G | 5 | a0001c0001t0014g0238 a0001c0001t0014g0240 a0001c0001t0014g0241 others(2): Show |
5 | HG01109.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2122-676A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160436 | |||||||
| chr14:92160501 | G | A | 1 | a0001c0001t0159g0075 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2122-611G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160501 | |||||||
| chr14:92160663 | A | G | 4 | a0001c0001t0006g0204 a0001c0001t0013g0210 a0001c0001t0137g0198 others(1): Show |
4 | HG00673.hp1 HG02080.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2122-449A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160663 | |||||||
| chr14:92160706 | A | G | 1 | a0001c0001t0157g0100 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2122-406A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160706 | |||||||
| chr14:92160725 | C | T | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.2122-387C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160725 | |||||||
| chr14:92160746 | G | A | 1 | a0001c0001t0166g0098 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2122-366G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160746 | |||||||
| chr14:92160794 | G | T | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.2122-318G>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160794 | |||||||
| chr14:92160816 | G | A | 57 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0041 others(54): Show |
72 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.2122-296G>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160816 | |||||||
| chr14:92160996 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.2122-116C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92160996 | |||||||
| chr14:92161065 | C | T | 2 | a0001c0001t0010g0061 a0001c0001t0049g0027 |
3 | HG01069.hp1 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2122-47C>T | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 14/15 | chr14 | 92161065 | |||||||
| chr14:92161308 | A | C | 4 | a0001c0001t0005g0212 a0001c0001t0017g0019 a0001c0001t0043g0019 others(1): Show |
5 | HG02280.hp1 HG02451.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2256+62A>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161308 | |||||||
| chr14:92161324 | T | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
313 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.2256+78T>A | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161324 | |||||||
| chr14:92161357 | T | G | 32 | a0001c0001t0020g0011 a0001c0001t0021g0004 a0001c0001t0021g0121 others(29): Show |
37 | HG00408.hp2 HG02040.hp2 HG02165.hp1 others(34): Show |
intron_variant | MODIFIER | c.2256+111T>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161357 | |||||||
| chr14:92161366 | T | C | 138 | a0001c0001t0003g0007 a0001c0001t0003g0010 a0001c0001t0003g0026 others(135): Show |
146 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.2256+120T>C | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161366 | |||||||
| chr14:92161562 | A | G | 1 | a0001c0001t0113g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2257-90A>G | CPSF2 | ENSG00000165934.13 | transcript | ENST00000298875.9 | protein_coding | 15/15 | chr14 | 92161562 |