Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11052 |
| ensemblid | ENSG00000111605.18 |
| hgncid | 13871 |
| symbol | CPSF6 |
| name | cleavage and polyadenylation specific factor 6 |
| refseq_nuc | NM_007007.3 |
| refseq_prot | NP_008938.2 |
| ensembl_nuc | ENST00000435070.7 |
| ensembl_prot | ENSP00000391774.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 69239569 |
| end | 69274358 |
| strand | + |
| ver | v1.2 |
| region | chr12:69239569-69274358 |
| region5000 | chr12:69234569-69279358 |
| regionname0 | CPSF6_chr12_69239569_69274358 |
| regionname5000 | CPSF6_chr12_69234569_69279358 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1653 | 234 | 47 | 44 | 110 | 10 | 22 | CPSF6_chr12_69234569_69279358 | CPSF6 | ATGGC others(1648): Show |
chr12 | 69234569 | 69279358 | ||
| a0001c0002 | 0/1 | 1653 | 151 | 33 | 25 | 77 | 1 | 14 | CPSF6_chr12_69234569_69279358 | CPSF6 | ATGGC others(1648): Show |
chr12 | 69234569 | 69279358 | ||
| a0001c0003 | 0/0 | 1653 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | ATGGC others(1648): Show |
chr12 | 69234569 | 69279358 | ||
| a0001c0004 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | ATGGC others(1648): Show |
chr12 | 69234569 | 69279358 | ||
| a0001c0005 | 0/0 | 1653 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | ATGGC others(1648): Show |
chr12 | 69234569 | 69279358 | ||
| a0001c0006 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | ATGGC others(1648): Show |
chr12 | 69234569 | 69279358 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/0 | 6584 | 50 | 6 | 11 | 29 | 1 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0003 | 0/0 | 6593 | 30 | 0 | 6 | 17 | 0 | 7 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6588): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0004 | 0/0 | 6589 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0005 | 0/0 | 6589 | 17 | 1 | 8 | 4 | 2 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0007 | 0/0 | 6583 | 10 | 0 | 0 | 10 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6578): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0008 | 0/0 | 6594 | 9 | 0 | 0 | 9 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6589): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0009 | 0/0 | 6584 | 8 | 0 | 0 | 8 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0010 | 0/0 | 6594 | 8 | 0 | 0 | 7 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6589): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0011 | 0/0 | 6585 | 6 | 0 | 3 | 1 | 1 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6580): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0013 | 0/0 | 6586 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6581): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0014 | 0/0 | 6587 | 5 | 2 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6582): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0015 | 0/0 | 6596 | 5 | 0 | 0 | 5 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6591): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0016 | 0/0 | 6589 | 4 | 0 | 2 | 0 | 2 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0017 | 0/0 | 6584 | 4 | 1 | 3 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0018 | 0/0 | 6591 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6586): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0019 | 0/0 | 6589 | 3 | 2 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0020 | 0/0 | 6591 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6586): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0021 | 0/0 | 6592 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6587): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0022 | 0/0 | 6584 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0023 | 0/0 | 6593 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6588): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0027 | 0/0 | 6590 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0028 | 0/0 | 6589 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0029 | 0/0 | 6582 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6577): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0030 | 0/0 | 6590 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0031 | 0/0 | 6589 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0032 | 0/0 | 6585 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6580): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0033 | 0/0 | 6589 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0034 | 0/0 | 6593 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6588): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0038 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0040 | 0/0 | 6595 | 2 | 0 | 0 | 1 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6590): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0042 | 0/0 | 6595 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6590): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0043 | 0/0 | 6597 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6592): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0044 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCCAG others(6581): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0045 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0046 | 0/0 | 6579 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6574): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0047 | 0/0 | 6585 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6580): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0049 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6582): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0050 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0051 | 0/0 | 6593 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6588): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0052 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0053 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0054 | 0/0 | 6584 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0055 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0056 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0057 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0058 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0059 | 0/0 | 6589 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0060 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6582): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0061 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6581): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0062 | 0/0 | 6585 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6580): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0063 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0064 | 0/0 | 6594 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6589): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0065 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0066 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0067 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6589): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0070 | 0/0 | 6594 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6589): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0073 | 0/0 | 6592 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6587): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0074 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6586): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0077 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6581): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0078 | 0/0 | 6587 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6582): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0079 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0083 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6586): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0085 | 0/0 | 6593 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6588): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0086 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6590): Show |
chr12 | 69234569 | 69279358 |
| a0001c0001t0090 | 0/0 | 6593 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6588): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0001 | 0/1 | 6588 | 67 | 15 | 18 | 24 | 0 | 9 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0004 | 0/0 | 6589 | 28 | 0 | 0 | 27 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0006 | 0/0 | 6590 | 14 | 3 | 0 | 11 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0008 | 0/0 | 6594 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6589): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0009 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0012 | 0/0 | 6589 | 6 | 5 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0024 | 0/0 | 6586 | 3 | 0 | 0 | 0 | 0 | 3 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6581): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0025 | 0/0 | 6589 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0026 | 0/0 | 6587 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6582): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0035 | 0/0 | 6588 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0036 | 0/0 | 6588 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0037 | 0/0 | 6590 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0039 | 0/0 | 6588 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0041 | 0/0 | 6590 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0048 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0068 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0069 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0071 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0072 | 0/0 | 6592 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6587): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0075 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0076 | 0/0 | 6588 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0080 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6586): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0081 | 0/0 | 6592 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6587): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0082 | 0/0 | 6590 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0084 | 0/0 | 6592 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6587): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0087 | 0/0 | 6589 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6584): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0088 | 0/0 | 6590 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0089 | 0/0 | 6588 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0002t0091 | 0/0 | 6590 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6585): Show |
chr12 | 69234569 | 69279358 |
| a0001c0003t0002 | 0/0 | 6584 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0003t0038 | 0/0 | 6584 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6579): Show |
chr12 | 69234569 | 69279358 |
| a0001c0004t0013 | 0/0 | 6586 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6581): Show |
chr12 | 69234569 | 69279358 |
| a0001c0005t0001 | 0/0 | 6588 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6583): Show |
chr12 | 69234569 | 69279358 |
| a0001c0006t0003 | 0/0 | 6593 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | GCTAG others(6588): Show |
chr12 | 69234569 | 69279358 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0020 | 1/0 | 3 | 0 | 0 | 0 | 1 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0002 | 0/0 | 14 | 0 | 4 | 5 | 0 | 5 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0005 | 0/0 | 6 | 0 | 2 | 3 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0007g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0008g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0009g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0010g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0010g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0010g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0011g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0011g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0011g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0011g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0011g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0014g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0014g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0014g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0014g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0015g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0015g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0015g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0015g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0016g0005 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0016g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0017g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0017g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0018g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0018g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0019g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0019g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0020g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0020g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0020g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0021g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0021g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0021g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0022g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0022g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0022g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0023g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0027g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0028g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0029g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0029g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0030g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0030g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0031g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0031g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0032g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0032g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0033g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0033g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0034g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0034g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0038g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0040g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0040g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0042g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0042g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0043g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0044g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0045g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0046g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0047g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0049g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0050g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0051g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0052g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0053g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0054g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0055g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0056g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0057g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0058g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0059g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0060g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0061g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0062g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0063g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0064g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0065g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0066g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0067g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0070g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0073g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0074g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0077g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0078g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0079g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0083g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0085g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0086g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0001t0090g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0001 | 0/0 | 11 | 1 | 5 | 5 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0004g0001 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0012g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0024g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0024g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0025g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0025g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0025g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0026g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0026g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0026g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0035g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0035g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0036g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0037g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0039g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0041g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0041g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0048g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0068g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0069g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0071g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0072g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0075g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0076g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0080g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0081g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0082g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0084g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0087g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0088g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0089g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0002t0091g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0003t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0003t0038g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0004t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0004t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0005t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| a0001c0006t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0023 | EUR | FIN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00280 | hp2 | a0001 | c0006 | t0003 | g0002 | EUR | FIN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0005 | EUR | FIN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00323 | hp2 | a0001 | c0001 | t0011 | g0202 | EUR | FIN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00438 | hp1 | a0001 | c0002 | t0004 | g0035 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00438 | hp2 | a0001 | c0001 | t0009 | g0004 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00544 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00558 | hp2 | a0001 | c0003 | t0002 | g0014 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00597 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00639 | hp1 | a0001 | c0001 | t0078 | g0017 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00639 | hp2 | a0001 | c0001 | t0011 | g0165 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00642 | hp1 | a0001 | c0001 | t0028 | g0047 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00673 | hp1 | a0001 | c0002 | t0006 | g0130 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00673 | hp2 | a0001 | c0001 | t0038 | g0195 | EAS | CHS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00733 | hp2 | a0001 | c0001 | t0023 | g0013 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00738 | hp1 | a0001 | c0002 | t0026 | g0003 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00738 | hp2 | a0001 | c0001 | t0029 | g0179 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0183 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0043 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01069 | hp1 | a0001 | c0002 | t0035 | g0122 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01070 | hp2 | a0001 | c0001 | t0023 | g0013 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01071 | hp2 | a0001 | c0002 | t0035 | g0123 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01106 | hp2 | a0001 | c0001 | t0028 | g0047 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01167 | hp1 | a0001 | c0001 | t0017 | g0004 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01167 | hp2 | a0001 | c0001 | t0019 | g0025 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01168 | hp1 | a0001 | c0002 | t0026 | g0176 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0190 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01169 | hp2 | a0001 | c0001 | t0017 | g0021 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01175 | hp2 | a0001 | c0001 | t0014 | g0027 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01192 | hp2 | a0001 | c0001 | t0059 | g0064 | AMR | PUR | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01256 | hp2 | a0001 | c0001 | t0016 | g0022 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01257 | hp2 | a0001 | c0001 | t0017 | g0021 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01258 | hp2 | a0001 | c0001 | t0016 | g0005 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01261 | hp1 | a0001 | c0001 | t0011 | g0043 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01346 | hp1 | a0001 | c0002 | t0076 | g0019 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01361 | hp2 | a0001 | c0002 | t0012 | g0007 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0188 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01433 | hp2 | a0001 | c0002 | t0025 | g0038 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01516 | hp1 | a0001 | c0001 | t0014 | g0066 | EUR | IBS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01516 | hp2 | a0001 | c0001 | t0016 | g0005 | EUR | IBS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01517 | hp1 | a0001 | c0002 | t0026 | g0057 | EUR | IBS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01517 | hp2 | a0001 | c0001 | t0016 | g0005 | EUR | IBS | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01884 | hp1 | a0001 | c0002 | t0012 | g0007 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01884 | hp2 | a0001 | c0001 | t0049 | g0050 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01891 | hp1 | a0001 | c0002 | t0006 | g0110 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01928 | hp2 | a0001 | c0005 | t0001 | g0105 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01978 | hp2 | a0001 | c0001 | t0070 | g0013 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02015 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02027 | hp2 | a0001 | c0002 | t0041 | g0120 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02040 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02040 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0046 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02055 | hp2 | a0001 | c0002 | t0069 | g0107 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02056 | hp2 | a0001 | c0001 | t0009 | g0155 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02080 | hp1 | a0001 | c0001 | t0067 | g0002 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02080 | hp2 | a0001 | c0001 | t0056 | g0009 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02083 | hp1 | a0001 | c0001 | t0052 | g0162 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02132 | hp1 | a0001 | c0002 | t0004 | g0035 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02135 | hp1 | a0001 | c0001 | t0011 | g0045 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02135 | hp2 | a0001 | c0002 | t0004 | g0106 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02145 | hp1 | a0001 | c0001 | t0043 | g0028 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CDX | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | CDX | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02258 | hp1 | a0001 | c0001 | t0017 | g0004 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02300 | hp1 | a0001 | c0001 | t0014 | g0027 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02451 | hp2 | a0001 | c0002 | t0036 | g0016 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02523 | hp1 | a0001 | c0001 | t0007 | g0134 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02572 | hp1 | a0001 | c0002 | t0068 | g0089 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02572 | hp2 | a0001 | c0001 | t0033 | g0147 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02602 | hp1 | a0001 | c0001 | t0046 | g0022 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02602 | hp2 | a0001 | c0001 | t0053 | g0152 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02615 | hp1 | a0001 | c0001 | t0079 | g0017 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02683 | hp1 | a0001 | c0001 | t0086 | g0073 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02698 | hp1 | a0001 | c0001 | t0011 | g0192 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0189 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02717 | hp1 | a0001 | c0002 | t0091 | g0114 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02717 | hp2 | a0001 | c0001 | t0055 | g0208 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02723 | hp2 | a0001 | c0001 | t0030 | g0139 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02735 | hp1 | a0001 | c0001 | t0018 | g0005 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02818 | hp1 | a0001 | c0002 | t0012 | g0007 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02818 | hp2 | a0001 | c0001 | t0021 | g0181 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02886 | hp1 | a0001 | c0002 | t0081 | g0097 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02895 | hp2 | a0001 | c0002 | t0072 | g0007 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02896 | hp1 | a0001 | c0002 | t0012 | g0007 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02896 | hp2 | a0001 | c0001 | t0065 | g0156 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02897 | hp1 | a0001 | c0002 | t0012 | g0088 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02922 | hp1 | a0001 | c0001 | t0033 | g0148 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02965 | hp1 | a0001 | c0001 | t0029 | g0178 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0207 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02976 | hp2 | a0001 | c0001 | t0058 | g0069 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03098 | hp1 | a0001 | c0001 | t0020 | g0141 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03098 | hp2 | a0001 | c0001 | t0060 | g0144 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0209 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03139 | hp2 | a0001 | c0002 | t0036 | g0016 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0140 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03195 | hp2 | a0001 | c0002 | t0037 | g0033 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03209 | hp1 | a0001 | c0002 | t0012 | g0007 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03209 | hp2 | a0001 | c0001 | t0032 | g0146 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03225 | hp1 | a0001 | c0001 | t0032 | g0145 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03225 | hp2 | a0001 | c0001 | t0027 | g0051 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03239 | hp2 | a0001 | c0002 | t0024 | g0003 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03453 | hp1 | a0001 | c0001 | t0050 | g0025 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03453 | hp2 | a0001 | c0001 | t0031 | g0170 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03486 | hp1 | a0001 | c0001 | t0030 | g0138 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03486 | hp2 | a0001 | c0002 | t0037 | g0033 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0003 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03516 | hp2 | a0001 | c0001 | t0021 | g0059 | AFR | ESN | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03688 | hp1 | a0001 | c0001 | t0054 | g0062 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03688 | hp2 | a0001 | c0002 | t0024 | g0111 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03704 | hp1 | a0001 | c0002 | t0004 | g0108 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03704 | hp2 | a0001 | c0001 | t0018 | g0005 | SAS | PJL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0125 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0002 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0079 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03942 | hp1 | a0001 | c0002 | t0024 | g0003 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0184 | SAS | BEB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG04115 | hp2 | a0001 | c0001 | t0040 | g0087 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG04199 | hp1 | a0001 | c0001 | t0018 | g0191 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG04204 | hp1 | a0001 | c0001 | t0085 | g0085 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | STU | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18522 | hp2 | a0001 | c0002 | t0006 | g0003 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | CHB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | CHB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18747 | hp1 | a0001 | c0001 | t0022 | g0159 | EAS | CHB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | CHB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18906 | hp1 | a0001 | c0001 | t0043 | g0028 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18906 | hp2 | a0001 | c0002 | t0071 | g0016 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18942 | hp2 | a0001 | c0002 | t0004 | g0175 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18944 | hp2 | a0001 | c0002 | t0082 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18945 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18946 | hp2 | a0001 | c0002 | t0039 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18947 | hp2 | a0001 | c0002 | t0088 | g0010 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18948 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18949 | hp1 | a0001 | c0001 | t0047 | g0186 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18949 | hp2 | a0001 | c0001 | t0015 | g0081 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18950 | hp1 | a0001 | c0001 | t0008 | g0080 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18950 | hp2 | a0001 | c0002 | t0087 | g0034 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18953 | hp2 | a0001 | c0002 | t0041 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0077 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18956 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18956 | hp2 | a0001 | c0001 | t0034 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18957 | hp1 | a0001 | c0002 | t0025 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18959 | hp1 | a0001 | c0002 | t0006 | g0126 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18960 | hp1 | a0001 | c0001 | t0040 | g0082 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18961 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18961 | hp2 | a0001 | c0001 | t0007 | g0164 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18963 | hp2 | a0001 | c0001 | t0022 | g0157 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18964 | hp2 | a0001 | c0002 | t0006 | g0041 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18965 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18966 | hp1 | a0001 | c0002 | t0006 | g0171 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18967 | hp1 | a0001 | c0002 | t0080 | g0010 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18970 | hp1 | a0001 | c0001 | t0015 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18970 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18971 | hp2 | a0001 | c0001 | t0062 | g0049 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18972 | hp1 | a0001 | c0002 | t0048 | g0012 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18974 | hp2 | a0001 | c0001 | t0090 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18975 | hp1 | a0001 | c0003 | t0002 | g0014 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18975 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18977 | hp2 | a0001 | c0002 | t0006 | g0129 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18979 | hp2 | a0001 | c0001 | t0074 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18980 | hp1 | a0001 | c0001 | t0009 | g0169 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18980 | hp2 | a0001 | c0001 | t0042 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18982 | hp1 | a0001 | c0002 | t0004 | g0104 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18982 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18983 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18984 | hp1 | a0001 | c0002 | t0006 | g0127 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18984 | hp2 | a0001 | c0001 | t0015 | g0032 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18986 | hp2 | a0001 | c0001 | t0083 | g0031 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18988 | hp1 | a0001 | c0001 | t0010 | g0029 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18988 | hp2 | a0001 | c0002 | t0039 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18989 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18991 | hp1 | a0001 | c0001 | t0034 | g0093 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18994 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18994 | hp2 | a0001 | c0001 | t0022 | g0168 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18995 | hp2 | a0001 | c0001 | t0015 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18998 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18998 | hp2 | a0001 | c0001 | t0015 | g0075 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18999 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18999 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19006 | hp1 | a0001 | c0001 | t0010 | g0029 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19006 | hp2 | a0001 | c0002 | t0006 | g0128 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19009 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19010 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19011 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19012 | hp1 | a0001 | c0002 | t0025 | g0003 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0182 | AFR | LWK | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19043 | hp2 | a0001 | c0001 | t0057 | g0177 | AFR | LWK | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19054 | hp2 | a0001 | c0002 | t0008 | g0090 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19058 | hp1 | a0001 | c0003 | t0038 | g0014 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19058 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19060 | hp1 | a0001 | c0002 | t0006 | g0041 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19060 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19064 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19066 | hp1 | a0001 | c0001 | t0009 | g0049 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19068 | hp1 | a0001 | c0001 | t0061 | g0011 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19070 | hp1 | a0001 | c0001 | t0007 | g0163 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19076 | hp1 | a0001 | c0002 | t0009 | g0095 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19076 | hp2 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19077 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19078 | hp1 | a0001 | c0001 | t0042 | g0084 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19078 | hp2 | a0001 | c0001 | t0044 | g0205 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19080 | hp1 | a0001 | c0001 | t0010 | g0070 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0124 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19083 | hp2 | a0001 | c0002 | t0084 | g0172 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19085 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19087 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19090 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19091 | hp2 | a0001 | c0002 | t0075 | g0099 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19240 | hp1 | a0001 | c0001 | t0031 | g0204 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA19240 | hp2 | a0001 | c0001 | t0019 | g0025 | AFR | YRI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ASW | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20129 | hp2 | a0001 | c0001 | t0021 | g0046 | AFR | ASW | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20752 | hp1 | a0001 | c0001 | t0023 | g0013 | EUR | TSI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | TSI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20805 | hp1 | a0001 | c0001 | t0045 | g0150 | EUR | TSI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20805 | hp2 | a0001 | c0001 | t0051 | g0137 | EUR | TSI | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | GIH | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20905 | hp2 | a0001 | c0002 | t0089 | g0003 | SAS | GIH | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02109 | hp2 | a0001 | c0001 | t0066 | g0143 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02486 | hp1 | a0001 | c0001 | t0064 | g0193 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02486 | hp2 | a0001 | c0004 | t0013 | g0197 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02559 | hp1 | a0001 | c0001 | t0019 | g0050 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG02559 | hp2 | a0001 | c0001 | t0077 | g0017 | AFR | ACB | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG03471 | hp2 | a0001 | c0004 | t0013 | g0173 | AFR | MSL | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG06807 | hp1 | a0001 | c0001 | t0020 | g0180 | AFR | USA | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0058 | AFR | USA | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA18955 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | USA | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA20300 | hp2 | a0001 | c0001 | t0063 | g0063 | AFR | USA | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA21309 | hp1 | a0001 | c0001 | t0073 | g0142 | AFR | LWK | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| NA21309 | hp2 | a0001 | c0001 | t0027 | g0051 | AFR | LWK | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0194 | REF | REF | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0020 | REF | REF | CPSF6_chr12_69234569_69279358 | CPSF6 | chr12 | 69234569 | 69279358 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69251284 | T | G | 1 | a0001c0004 | 2 | HG02486.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.216T>G | p.Val72Val | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/10 | 294/6584 | 216/1656 | 72/551 | chr12 | 69251284 | |||
| chr12:69253134 | G | A | 2 | a0001c0002 a0001c0005 |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
synonymous_variant | LOW | c.354G>A | p.Arg118Arg | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/10 | 432/6584 | 354/1656 | 118/551 | chr12 | 69253134 | |||
| chr12:69258948 | A | G | 1 | a0001c0006 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.1053A>G | p.Pro351Pro | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/10 | 1131/6584 | 1053/1656 | 351/551 | chr12 | 69258948 | |||
| chr12:69258960 | G | A | 1 | a0001c0003 | 3 | HG00558.hp2 NA18975.hp1 NA19058.hp1 |
synonymous_variant | LOW | c.1065G>A | p.Pro355Pro | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/10 | 1143/6584 | 1065/1656 | 355/551 | chr12 | 69258960 | |||
| chr12:69260183 | T | C | 1 | a0001c0005 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1455T>C | p.Tyr485Tyr | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/10 | 1533/6584 | 1455/1656 | 485/551 | chr12 | 69260183 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69239571 | T | C | 1 | a0001c0001t0044 | 1 | NA19078.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/10 | 76 | chr12 | 69239571 | ||||||
| chr12:69239599 | A | G | 52 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(49): Show |
227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
5_prime_UTR_variant | MODIFIER | c.-48A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/10 | 48 | chr12 | 69239599 | ||||||
| chr12:69239636 | G | A | 1 | a0001c0001t0045 | 1 | NA20805.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/10 | 11 | chr12 | 69239636 | ||||||
| chr12:69269567 | C | T | 1 | a0001c0001t0043 | 2 | HG02145.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*59C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7008 | chr12 | 69269567 | ||||||
| chr12:69269759 | A | G | 1 | a0001c0002t0091 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*251A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7200 | chr12 | 69269759 | ||||||
| chr12:69269782 | T | C | 1 | a0001c0001t0027 | 2 | HG03225.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*274T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7223 | chr12 | 69269782 | ||||||
| chr12:69269805 | A | G | 1 | a0001c0001t0027 | 2 | HG03225.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*297A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7246 | chr12 | 69269805 | ||||||
| chr12:69269905 | A | G | 1 | a0001c0001t0066 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7346 | chr12 | 69269905 | ||||||
| chr12:69270065 | G | A | 2 | a0001c0001t0034 a0001c0001t0067 |
3 | HG02080.hp1 NA18956.hp2 NA18991.hp1 |
3_prime_UTR_variant | MODIFIER | c.*557G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7506 | chr12 | 69270065 | ||||||
| chr12:69270072 | G | C | 6 | a0001c0001t0005 a0001c0001t0016 a0001c0001t0018 others(3): Show |
28 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*564G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7513 | chr12 | 69270072 | ||||||
| chr12:69270073 | A | G | 1 | a0001c0001t0028 | 2 | HG00642.hp1 HG01106.hp2 |
3_prime_UTR_variant | MODIFIER | c.*565A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7514 | chr12 | 69270073 | ||||||
| chr12:69270205 | T | A | 1 | a0001c0002t0048 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*697T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7646 | chr12 | 69270205 | ||||||
| chr12:69270356 | T | C | 1 | a0001c0002t0068 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*848T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 7797 | chr12 | 69270356 | ||||||
| chr12:69270620 | A | G | 2 | a0001c0001t0065 a0001c0001t0066 |
2 | HG02109.hp2 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1112A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8061 | chr12 | 69270620 | ||||||
| chr12:69270714 | A | T | 1 | a0001c0001t0090 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8155 | chr12 | 69270714 | ||||||
| chr12:69270799 | G | A | 1 | a0001c0002t0035 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1291G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8240 | chr12 | 69270799 | ||||||
| chr12:69270822 | G | T | 1 | a0001c0001t0064 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8263 | chr12 | 69270822 | ||||||
| chr12:69270856 | C | G | 1 | a0001c0001t0033 | 2 | HG02572.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1348C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8297 | chr12 | 69270856 | ||||||
| chr12:69270862 | T | C | 3 | a0001c0001t0019 a0001c0001t0049 a0001c0001t0050 |
5 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1354T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8303 | chr12 | 69270862 | ||||||
| chr12:69271046 | T | C | 1 | a0001c0002t0069 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1538T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8487 | chr12 | 69271046 | ||||||
| chr12:69271271 | A | G | 1 | a0001c0001t0063 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1763A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8712 | chr12 | 69271271 | ||||||
| chr12:69271278 | C | A | 1 | a0001c0001t0064 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1770C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8719 | chr12 | 69271278 | ||||||
| chr12:69271455 | G | T | 1 | a0001c0002t0089 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1947G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8896 | chr12 | 69271455 | ||||||
| chr12:69271529 | T | C | 3 | a0001c0001t0023 a0001c0001t0051 a0001c0001t0070 |
5 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2021T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 8970 | chr12 | 69271529 | ||||||
| chr12:69271742 | A | G | 5 | a0001c0001t0009 a0001c0001t0044 a0001c0001t0061 others(2): Show |
12 | HG00438.hp2 HG02056.hp2 NA18971.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2234A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9183 | chr12 | 69271742 | ||||||
| chr12:69271830 | T | G | 1 | a0001c0001t0064 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2322T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9271 | chr12 | 69271830 | ||||||
| chr12:69271855 | C | T | 1 | a0001c0002t0088 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2347C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9296 | chr12 | 69271855 | ||||||
| chr12:69272012 | G | T | 1 | a0001c0002t0087 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2504G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9453 | chr12 | 69272012 | ||||||
| chr12:69272152 | T | C | 1 | a0001c0001t0052 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2644T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9593 | chr12 | 69272152 | ||||||
| chr12:69272155 | G | GT | 33 | a0001c0001t0005 a0001c0001t0016 a0001c0001t0018 others(30): Show |
142 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*2659dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9609 | INFO_REALIGN_3_PRIME | chr12 | 69272155 | |||||
| chr12:69272155 | G | GTT | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(15): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2658_*2659dupTT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9609 | INFO_REALIGN_3_PRIME | chr12 | 69272155 | |||||
| chr12:69272155 | G | GTTT | 4 | a0001c0001t0008 a0001c0001t0042 a0001c0002t0008 others(1): Show |
14 | HG02027.hp2 HG02040.hp1 NA18946.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2657_*2659dupTTT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9609 | INFO_REALIGN_3_PRIME | chr12 | 69272155 | |||||
| chr12:69272156 | T | G | 1 | a0001c0001t0053 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2648T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9597 | chr12 | 69272156 | ||||||
| chr12:69272178 | A | G | 1 | a0001c0001t0086 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2670A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9619 | chr12 | 69272178 | ||||||
| chr12:69272268 | A | C | 1 | a0001c0001t0086 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2760A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9709 | chr12 | 69272268 | ||||||
| chr12:69272295 | A | T | 1 | a0001c0001t0060 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2787A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9736 | chr12 | 69272295 | ||||||
| chr12:69272499 | A | G | 1 | a0001c0001t0050 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2991A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 9940 | chr12 | 69272499 | ||||||
| chr12:69272782 | G | A | 1 | a0001c0001t0054 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3274G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10223 | chr12 | 69272782 | ||||||
| chr12:69272847 | C | T | 3 | a0001c0001t0023 a0001c0001t0051 a0001c0001t0070 |
5 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3339C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10288 | chr12 | 69272847 | ||||||
| chr12:69272859 | C | G | 1 | a0001c0001t0022 | 3 | NA18747.hp1 NA18963.hp2 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3351C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10300 | chr12 | 69272859 | ||||||
| chr12:69272869 | A | AGT | 23 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0020 others(20): Show |
49 | HG00639.hp1 HG00673.hp1 HG01175.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3388_*3389dupGT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10339 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | |||||
| chr12:69272869 | A | AGTGT | 16 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0010 others(13): Show |
64 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3386_*3389dupGTGT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10339 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | |||||
| chr12:69272869 | A | AGTGTGT | 7 | a0001c0001t0015 a0001c0001t0031 a0001c0001t0033 others(4): Show |
14 | HG02109.hp2 HG02572.hp2 HG02683.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3384_*3389dupGTGT others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10339 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | |||||
| chr12:69272869 | A | AGTGTGTG others(1): Show |
4 | a0001c0001t0023 a0001c0001t0043 a0001c0001t0051 others(1): Show |
7 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3382_*3389dupGTGT others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10339 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | |||||
| chr12:69272869 | AGT | A | 7 | a0001c0001t0005 a0001c0001t0016 a0001c0001t0028 others(4): Show |
32 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3388_*3389delGT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10337 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | |||||
| chr12:69272869 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0046 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3378_*3389delGTGT others(8): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10327 | INFO_REALIGN_3_PRIME | chr12 | 69272869 | |||||
| chr12:69272956 | A | G | 1 | a0001c0001t0056 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3448A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10397 | chr12 | 69272956 | ||||||
| chr12:69273260 | G | A | 1 | a0001c0001t0016 | 4 | HG01256.hp2 HG01258.hp2 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3752G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10701 | chr12 | 69273260 | ||||||
| chr12:69273295 | T | A | 51 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(48): Show |
226 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*3787T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10736 | chr12 | 69273295 | ||||||
| chr12:69273343 | A | G | 2 | a0001c0001t0017 a0001c0001t0045 |
5 | HG01167.hp1 HG01169.hp2 HG01257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3835A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 10784 | chr12 | 69273343 | ||||||
| chr12:69273680 | A | C | 1 | a0001c0002t0076 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4172A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11121 | chr12 | 69273680 | ||||||
| chr12:69273883 | C | G | 1 | a0001c0001t0058 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4375C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11324 | chr12 | 69273883 | ||||||
| chr12:69274003 | A | C | 1 | a0001c0001t0085 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4495A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11444 | chr12 | 69274003 | ||||||
| chr12:69274109 | C | CT | 9 | a0001c0001t0011 a0001c0001t0014 a0001c0001t0019 others(6): Show |
20 | HG00323.hp2 HG00639.hp2 HG00741.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4619dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | |||||
| chr12:69274109 | C | CTTT | 33 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(30): Show |
185 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*4617_*4619dupTTT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | |||||
| chr12:69274109 | C | CTTTT | 14 | a0001c0001t0010 a0001c0001t0015 a0001c0001t0027 others(11): Show |
31 | HG00544.hp2 HG01433.hp2 HG02080.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4616_*4619dupTTTT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | |||||
| chr12:69274109 | C | CTTTTT | 2 | a0001c0001t0020 a0001c0002t0012 |
9 | HG01361.hp2 HG01884.hp1 HG02818.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4615_*4619dupTTTT others(1): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | |||||
| chr12:69274109 | C | CTTTTTT | 11 | a0001c0001t0005 a0001c0001t0016 a0001c0001t0018 others(8): Show |
36 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4614_*4619dupTTTT others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11569 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | |||||
| chr12:69274109 | CT | C | 5 | a0001c0001t0007 a0001c0001t0031 a0001c0001t0033 others(2): Show |
16 | HG00597.hp1 HG02027.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4619delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11568 | INFO_REALIGN_3_PRIME | chr12 | 69274109 | |||||
| chr12:69274178 | C | T | 1 | a0001c0002t0075 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4670C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11619 | chr12 | 69274178 | ||||||
| chr12:69274225 | C | T | 1 | a0001c0002t0039 | 2 | NA18946.hp2 NA18988.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4717C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 10/10 | 11666 | chr12 | 69274225 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:69239765 | A | C | 8 | a0001c0001t0014g0207 a0001c0001t0014g0209 a0001c0001t0019g0025 others(5): Show |
10 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+59A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69239765 | |||||||
| chr12:69239892 | G | T | 4 | a0001c0001t0002g0206 a0001c0001t0009g0049 a0001c0001t0044g0205 others(1): Show |
4 | NA18971.hp2 NA19066.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+186G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69239892 | |||||||
| chr12:69239941 | G | C | 1 | a0001c0002t0001g0052 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.60+235G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69239941 | |||||||
| chr12:69239979 | G | C | 1 | a0001c0001t0003g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.60+273G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69239979 | |||||||
| chr12:69240061 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.60+355G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240061 | |||||||
| chr12:69240084 | C | T | 1 | a0001c0001t0031g0204 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.60+378C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240084 | |||||||
| chr12:69240105 | G | A | 1 | a0001c0002t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.60+399G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240105 | |||||||
| chr12:69240136 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.60+430G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240136 | |||||||
| chr12:69240147 | C | T | 1 | a0001c0002t0001g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.60+441C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240147 | |||||||
| chr12:69240168 | C | G | 1 | a0001c0002t0001g0048 | 2 | HG00609.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.60+462C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240168 | |||||||
| chr12:69240203 | C | T | 1 | a0001c0001t0011g0202 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.60+497C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240203 | |||||||
| chr12:69240206 | T | G | 1 | a0001c0002t0026g0057 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.60+500T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240206 | |||||||
| chr12:69240221 | G | A | 1 | a0001c0001t0003g0026 | 2 | NA18963.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.60+515G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240221 | |||||||
| chr12:69240229 | G | C | 2 | a0001c0001t0013g0058 a0001c0001t0021g0059 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.60+523G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240229 | |||||||
| chr12:69240251 | T | G | 1 | a0001c0002t0001g0060 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.60+545T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240251 | |||||||
| chr12:69240363 | C | T | 9 | a0001c0001t0002g0009 a0001c0001t0002g0024 a0001c0001t0002g0054 others(6): Show |
15 | HG01099.hp2 HG01981.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.60+657C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240363 | |||||||
| chr12:69240374 | A | G | 1 | a0001c0004t0013g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.60+668A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240374 | |||||||
| chr12:69240580 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.60+874A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240580 | |||||||
| chr12:69240858 | G | A | 1 | a0001c0001t0013g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.60+1152G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240858 | |||||||
| chr12:69240904 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.60+1198T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240904 | |||||||
| chr12:69240926 | G | A | 1 | a0001c0001t0054g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.60+1220G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69240926 | |||||||
| chr12:69241099 | G | T | 1 | a0001c0001t0038g0195 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.60+1393G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241099 | |||||||
| chr12:69241105 | C | T | 1 | a0001c0001t0014g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.60+1399C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241105 | |||||||
| chr12:69241530 | G | A | 7 | a0001c0001t0014g0207 a0001c0001t0014g0209 a0001c0001t0019g0025 others(4): Show |
8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+1824G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241530 | |||||||
| chr12:69241925 | C | CA | 12 | a0001c0001t0002g0065 a0001c0001t0014g0027 a0001c0001t0014g0066 others(9): Show |
14 | HG01167.hp2 HG01175.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+2233dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69241925 | ||||||
| chr12:69241925 | CA | C | 37 | a0001c0001t0002g0201 a0001c0001t0003g0174 a0001c0001t0005g0005 others(34): Show |
48 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.60+2233delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69241925 | ||||||
| chr12:69241956 | T | C | 1 | a0001c0004t0013g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.60+2250T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241956 | |||||||
| chr12:69241957 | T | C | 2 | a0001c0001t0013g0046 a0001c0001t0021g0046 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.60+2251T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69241957 | |||||||
| chr12:69242085 | C | A | 2 | a0001c0002t0036g0016 a0001c0002t0071g0016 |
3 | HG02451.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60+2379C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242085 | |||||||
| chr12:69242093 | T | C | 1 | a0001c0002t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.60+2387T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242093 | |||||||
| chr12:69242203 | T | TA | 136 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(133): Show |
222 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.60+2507dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69242203 | ||||||
| chr12:69242213 | A | C | 1 | a0001c0001t0064g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.60+2507A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242213 | |||||||
| chr12:69242246 | T | C | 1 | a0001c0001t0003g0068 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.60+2540T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242246 | |||||||
| chr12:69242302 | T | C | 1 | a0001c0001t0002g0132 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.60+2596T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242302 | |||||||
| chr12:69242305 | G | A | 3 | a0001c0001t0007g0133 a0001c0001t0007g0134 a0001c0001t0007g0135 |
3 | HG02027.hp1 HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.60+2599G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242305 | |||||||
| chr12:69242340 | A | G | 1 | a0001c0001t0003g0131 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.60+2634A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242340 | |||||||
| chr12:69242343 | CT | C | 7 | a0001c0001t0002g0136 a0001c0001t0014g0207 a0001c0001t0014g0209 others(4): Show |
8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+2641delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69242343 | ||||||
| chr12:69242444 | G | A | 3 | a0001c0001t0023g0013 a0001c0001t0051g0137 a0001c0001t0070g0013 |
5 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+2738G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242444 | |||||||
| chr12:69242534 | G | T | 77 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0012 others(74): Show |
123 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.60+2828G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242534 | |||||||
| chr12:69242542 | G | T | 1 | a0001c0001t0034g0093 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.60+2836G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242542 | |||||||
| chr12:69242831 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.60+3125G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242831 | |||||||
| chr12:69242901 | G | T | 1 | a0001c0001t0031g0170 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.60+3195G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242901 | |||||||
| chr12:69242916 | C | T | 7 | a0001c0001t0014g0207 a0001c0001t0014g0209 a0001c0001t0019g0025 others(4): Show |
8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+3210C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69242916 | |||||||
| chr12:69243092 | C | CA | 7 | a0001c0001t0020g0140 a0001c0001t0020g0141 a0001c0001t0030g0138 others(4): Show |
7 | HG02723.hp2 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+3396dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69243092 | ||||||
| chr12:69243224 | C | A | 1 | a0001c0001t0066g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.60+3518C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243224 | |||||||
| chr12:69243237 | G | A | 2 | a0001c0001t0029g0178 a0001c0001t0029g0179 |
2 | HG00738.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.60+3531G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243237 | |||||||
| chr12:69243259 | T | A | 1 | a0001c0002t0001g0094 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.60+3553T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243259 | |||||||
| chr12:69243381 | C | T | 6 | a0001c0002t0001g0006 a0001c0002t0001g0018 a0001c0002t0001g0067 others(3): Show |
14 | HG01069.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+3675C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243381 | |||||||
| chr12:69243680 | A | G | 1 | a0001c0002t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.60+3974A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243680 | |||||||
| chr12:69243888 | C | T | 1 | a0001c0001t0009g0169 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.60+4182C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243888 | |||||||
| chr12:69243889 | G | A | 1 | a0001c0001t0010g0070 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.60+4183G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69243889 | |||||||
| chr12:69244007 | A | T | 11 | a0001c0002t0006g0010 a0001c0002t0006g0041 a0001c0002t0006g0126 others(8): Show |
14 | HG00673.hp1 NA18945.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+4301A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244007 | |||||||
| chr12:69244057 | A | G | 6 | a0001c0002t0001g0006 a0001c0002t0001g0018 a0001c0002t0001g0067 others(3): Show |
14 | HG01069.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.60+4351A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244057 | |||||||
| chr12:69244067 | T | C | 190 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(187): Show |
291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.60+4361T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244067 | |||||||
| chr12:69244121 | G | T | 1 | a0001c0001t0034g0093 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.60+4415G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244121 | |||||||
| chr12:69244302 | C | G | 23 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(20): Show |
34 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.60+4596C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244302 | |||||||
| chr12:69244396 | G | C | 1 | a0001c0001t0027g0051 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.60+4690G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244396 | |||||||
| chr12:69244459 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.60+4753A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244459 | |||||||
| chr12:69244518 | T | C | 139 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(136): Show |
227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.60+4812T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244518 | |||||||
| chr12:69244638 | C | T | 1 | a0001c0001t0055g0208 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.60+4932C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244638 | |||||||
| chr12:69244695 | CT | C | 140 | a0001c0001t0002g0136 a0001c0001t0003g0002 a0001c0001t0003g0026 others(137): Show |
228 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.60+5000delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69244695 | ||||||
| chr12:69244780 | G | C | 1 | a0001c0001t0063g0063 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.60+5074G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244780 | |||||||
| chr12:69244830 | T | C | 190 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(187): Show |
291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.60+5124T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69244830 | |||||||
| chr12:69245096 | TA | T | 52 | a0001c0001t0002g0021 a0001c0001t0002g0132 a0001c0001t0002g0166 others(49): Show |
67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.60+5408delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69245096 | ||||||
| chr12:69245096 | TAA | T | 88 | a0001c0001t0005g0190 a0001c0002t0001g0001 a0001c0002t0001g0003 others(85): Show |
148 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.60+5407_60+5408del others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69245096 | ||||||
| chr12:69245098 | A | T | 1 | a0001c0001t0018g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.60+5392A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245098 | |||||||
| chr12:69245149 | A | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.60+5443A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245149 | |||||||
| chr12:69245215 | T | C | 1 | a0001c0002t0001g0018 | 3 | HG02647.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.60+5509T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245215 | |||||||
| chr12:69245271 | G | A | 1 | a0001c0001t0031g0204 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.60+5565G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245271 | |||||||
| chr12:69245295 | C | T | 1 | a0001c0002t0001g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.60+5589C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245295 | |||||||
| chr12:69245365 | C | G | 23 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(20): Show |
34 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.60+5659C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245365 | |||||||
| chr12:69245427 | G | A | 190 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(187): Show |
291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.61-5702G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245427 | |||||||
| chr12:69245435 | A | G | 190 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(187): Show |
291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.61-5694A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245435 | |||||||
| chr12:69245458 | T | G | 139 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(136): Show |
227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.61-5671T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245458 | |||||||
| chr12:69245805 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.61-5324G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245805 | |||||||
| chr12:69245879 | A | G | 7 | a0001c0001t0014g0207 a0001c0001t0014g0209 a0001c0001t0019g0025 others(4): Show |
8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-5250A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245879 | |||||||
| chr12:69245899 | A | G | 23 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(20): Show |
34 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.61-5230A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69245899 | |||||||
| chr12:69246055 | C | A | 1 | a0001c0002t0081g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.61-5074C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246055 | |||||||
| chr12:69246165 | G | C | 1 | a0001c0001t0020g0180 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.61-4964G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246165 | |||||||
| chr12:69246264 | A | G | 1 | a0001c0001t0040g0087 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.61-4865A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246264 | |||||||
| chr12:69246321 | T | C | 1 | a0001c0001t0002g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61-4808T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246321 | |||||||
| chr12:69246526 | A | G | 1 | a0001c0001t0073g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61-4603A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246526 | |||||||
| chr12:69246704 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.61-4425C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246704 | |||||||
| chr12:69246721 | C | G | 41 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(38): Show |
66 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.61-4408C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246721 | |||||||
| chr12:69246800 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.61-4329T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246800 | |||||||
| chr12:69246816 | A | G | 1 | a0001c0001t0085g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61-4313A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246816 | |||||||
| chr12:69246876 | C | T | 1 | a0001c0001t0033g0148 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.61-4253C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69246876 | |||||||
| chr12:69247093 | A | G | 1 | a0001c0001t0058g0069 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.61-4036A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247093 | |||||||
| chr12:69247122 | G | GA | 138 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(135): Show |
226 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.61-4001dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247122 | ||||||
| chr12:69247134 | A | G | 7 | a0001c0001t0002g0008 a0001c0001t0007g0008 a0001c0001t0007g0133 others(4): Show |
11 | HG00597.hp1 HG00621.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-3995A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247134 | |||||||
| chr12:69247207 | A | G | 1 | a0001c0001t0073g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.61-3922A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247207 | |||||||
| chr12:69247336 | T | C | 1 | a0001c0001t0063g0063 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.61-3793T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247336 | |||||||
| chr12:69247369 | G | GT | 18 | a0001c0001t0002g0044 a0001c0001t0002g0065 a0001c0001t0002g0158 others(15): Show |
21 | HG00408.hp1 HG01175.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.61-3746dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247369 | ||||||
| chr12:69247369 | G | GTT | 8 | a0001c0001t0002g0015 a0001c0001t0002g0045 a0001c0001t0002g0132 others(5): Show |
10 | HG00735.hp2 HG02083.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-3747_61-3746dup others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247369 | ||||||
| chr12:69247369 | G | T | 2 | a0001c0001t0029g0178 a0001c0001t0029g0179 |
2 | HG00738.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61-3760G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247369 | |||||||
| chr12:69247369 | GT | G | 12 | a0001c0001t0002g0200 a0001c0001t0014g0207 a0001c0001t0014g0209 others(9): Show |
15 | HG00733.hp2 HG01070.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.61-3746delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247369 | ||||||
| chr12:69247449 | ACAG | A | 41 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(38): Show |
66 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.61-3676_61-3674del others(3): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247449 | ||||||
| chr12:69247479 | T | G | 1 | a0001c0002t0004g0035 | 2 | HG00438.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.61-3650T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247479 | |||||||
| chr12:69247513 | C | A | 2 | a0001c0001t0029g0178 a0001c0001t0029g0179 |
2 | HG00738.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.61-3616C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247513 | |||||||
| chr12:69247567 | G | A | 1 | a0001c0001t0045g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-3562G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247567 | |||||||
| chr12:69247594 | T | C | 4 | a0001c0001t0031g0204 a0001c0001t0064g0193 a0001c0004t0013g0173 others(1): Show |
4 | HG02486.hp1 HG02486.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-3535T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69247594 | |||||||
| chr12:69247796 | T | TAA | 3 | a0001c0001t0010g0029 a0001c0001t0010g0070 a0001c0001t0042g0084 |
4 | NA18988.hp1 NA19006.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-3330_61-3329dup others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69247796 | ||||||
| chr12:69248035 | C | T | 2 | a0001c0002t0004g0035 a0001c0002t0004g0124 |
3 | HG00438.hp1 HG02132.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.61-3094C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248035 | |||||||
| chr12:69248365 | G | T | 2 | a0001c0002t0001g0019 a0001c0002t0076g0019 |
3 | HG01106.hp1 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.61-2764G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248365 | |||||||
| chr12:69248505 | T | A | 2 | a0001c0001t0013g0046 a0001c0001t0021g0046 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.61-2624T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248505 | |||||||
| chr12:69248535 | C | T | 193 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(190): Show |
294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.61-2594C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248535 | |||||||
| chr12:69248653 | G | A | 1 | a0001c0001t0007g0133 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.61-2476G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248653 | |||||||
| chr12:69248860 | A | G | 1 | a0001c0001t0063g0063 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.61-2269A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248860 | |||||||
| chr12:69248865 | C | T | 1 | a0001c0001t0014g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.61-2264C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248865 | |||||||
| chr12:69248866 | G | A | 2 | a0001c0001t0019g0025 a0001c0001t0050g0025 |
3 | HG01167.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.61-2263G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248866 | |||||||
| chr12:69248903 | A | T | 189 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(186): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.61-2226A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248903 | |||||||
| chr12:69248964 | C | T | 2 | a0001c0001t0007g0135 a0001c0004t0013g0197 |
2 | HG02486.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.61-2165C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248964 | |||||||
| chr12:69248968 | C | T | 1 | a0001c0001t0064g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.61-2161C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69248968 | |||||||
| chr12:69249012 | C | T | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.61-2117C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249012 | |||||||
| chr12:69249013 | G | A | 1 | a0001c0001t0022g0157 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.61-2116G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249013 | |||||||
| chr12:69249021 | C | T | 7 | a0001c0001t0013g0046 a0001c0001t0013g0058 a0001c0001t0013g0182 others(4): Show |
7 | HG02055.hp1 HG02818.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-2108C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249021 | |||||||
| chr12:69249092 | CTACAAAA others(2): Show |
C | 7 | a0001c0001t0002g0166 a0001c0001t0009g0011 a0001c0001t0009g0049 others(4): Show |
10 | HG02056.hp2 NA18971.hp2 NA18979.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-2031_61-2023del others(9): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249092 | ||||||
| chr12:69249133 | G | A | 139 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(136): Show |
227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.61-1996G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249133 | |||||||
| chr12:69249151 | TC | T | 8 | a0001c0001t0005g0005 a0001c0001t0005g0187 a0001c0001t0005g0188 others(5): Show |
17 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-1977delC | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249151 | |||||||
| chr12:69249151 | TCG | T | 8 | a0001c0001t0005g0022 a0001c0001t0005g0023 a0001c0001t0005g0184 others(5): Show |
10 | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.61-1977_61-1976del others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249151 | |||||||
| chr12:69249151 | TCGGGGGG others(4): Show |
T | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.61-1977_61-1967del others(11): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249151 | |||||||
| chr12:69249152 | C | CGGG | 22 | a0001c0001t0002g0004 a0001c0001t0002g0020 a0001c0001t0002g0024 others(19): Show |
25 | HG00558.hp2 HG00639.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.61-1962_61-1960dup others(3): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGGG | 16 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(13): Show |
21 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.61-1963_61-1960dup others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGGGGGG others(3): Show |
2 | a0001c0001t0009g0155 a0001c0001t0020g0141 |
2 | HG02056.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.61-1969_61-1960dup others(10): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGGGGGG others(5): Show |
2 | a0001c0001t0044g0205 a0001c0001t0057g0177 |
2 | NA19043.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.61-1971_61-1960dup others(12): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(3): Show |
13 | a0001c0002t0001g0001 a0001c0002t0001g0036 a0001c0002t0001g0039 others(10): Show |
14 | HG00558.hp1 HG01891.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(10): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(4): Show |
10 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(7): Show |
11 | HG01168.hp1 HG01346.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(11): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(5): Show |
8 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0019 others(5): Show |
8 | HG00609.hp1 HG00673.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(12): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(6): Show |
18 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0019 others(15): Show |
18 | HG00408.hp1 HG01106.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(13): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(7): Show |
14 | a0001c0002t0001g0001 a0001c0002t0001g0037 a0001c0002t0001g0038 others(11): Show |
14 | HG00609.hp2 HG01258.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(14): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(8): Show |
6 | a0001c0002t0001g0003 a0001c0002t0001g0012 a0001c0002t0001g0039 others(3): Show |
6 | HG00735.hp1 HG01069.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(15): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(9): Show |
5 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0061 others(2): Show |
7 | HG01099.hp1 HG01175.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(16): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(10): Show |
8 | a0001c0002t0001g0003 a0001c0002t0001g0098 a0001c0002t0001g0103 others(5): Show |
8 | HG01071.hp2 HG02135.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(17): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(11): Show |
3 | a0001c0002t0001g0001 a0001c0002t0001g0012 a0001c0002t0048g0012 |
3 | HG01952.hp2 NA18954.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(18): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(12): Show |
1 | a0001c0002t0001g0012 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.61-1975_61-1974ins others(19): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(17): Show |
1 | a0001c0002t0001g0101 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61-1975_61-1974ins others(24): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(18): Show |
1 | a0001c0002t0025g0001 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.61-1975_61-1974ins others(25): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | CGGTGGGG others(28): Show |
1 | a0001c0002t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.61-1975_61-1974ins others(35): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249152 | ||||||
| chr12:69249152 | C | G | 6 | a0001c0001t0002g0153 a0001c0001t0005g0183 a0001c0001t0007g0134 others(3): Show |
6 | HG00733.hp1 HG00741.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-1977C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249152 | |||||||
| chr12:69249154 | G | GT | 6 | a0001c0002t0004g0001 a0001c0002t0004g0034 a0001c0002t0004g0035 others(3): Show |
11 | HG00597.hp2 HG00621.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-1975_61-1974ins others(1): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249154 | |||||||
| chr12:69249155 | G | T | 10 | a0001c0002t0001g0109 a0001c0002t0004g0001 a0001c0002t0004g0035 others(7): Show |
21 | HG00438.hp1 HG02027.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.61-1974G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249155 | |||||||
| chr12:69249156 | G | A | 3 | a0001c0001t0002g0044 a0001c0001t0002g0158 a0001c0001t0002g0167 |
4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1973G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249156 | |||||||
| chr12:69249157 | G | T | 1 | a0001c0002t0001g0001 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.61-1972G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249157 | |||||||
| chr12:69249161 | G | T | 2 | a0001c0001t0013g0046 a0001c0001t0021g0046 |
2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.61-1968G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249161 | |||||||
| chr12:69249163 | G | C | 2 | a0001c0001t0033g0147 a0001c0001t0033g0148 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61-1966G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249163 | |||||||
| chr12:69249163 | G | GGGGGGGG others(8): Show |
1 | a0001c0001t0002g0136 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.61-1960_61-1959ins others(15): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249163 | ||||||
| chr12:69249163 | G | T | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.61-1966G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249163 | |||||||
| chr12:69249167 | G | A | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.61-1962G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249167 | |||||||
| chr12:69249168 | G | C | 98 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(95): Show |
166 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.61-1961G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249168 | |||||||
| chr12:69249188 | G | A | 2 | a0001c0004t0013g0173 a0001c0004t0013g0197 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.61-1941G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249188 | |||||||
| chr12:69249255 | AG | A | 2 | a0001c0001t0011g0043 a0001c0001t0011g0165 |
3 | HG00639.hp2 HG00741.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.61-1873delG | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249255 | |||||||
| chr12:69249257 | C | T | 2 | a0001c0001t0011g0043 a0001c0001t0011g0165 |
3 | HG00639.hp2 HG00741.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.61-1872C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249257 | |||||||
| chr12:69249266 | G | A | 3 | a0001c0001t0003g0071 a0001c0004t0013g0173 a0001c0004t0013g0197 |
3 | HG02083.hp2 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.61-1863G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249266 | |||||||
| chr12:69249282 | TAAATAA | T | 13 | a0001c0001t0013g0058 a0001c0001t0020g0140 a0001c0001t0020g0141 others(10): Show |
13 | HG02572.hp2 HG02723.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-1842_61-1837del others(6): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249282 | ||||||
| chr12:69249287 | A | T | 17 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(14): Show |
28 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.61-1842A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249287 | |||||||
| chr12:69249293 | T | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0167 |
3 | HG02809.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.61-1836T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249293 | |||||||
| chr12:69249353 | A | G | 1 | a0001c0001t0022g0168 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.61-1776A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249353 | |||||||
| chr12:69249371 | A | G | 2 | a0001c0002t0035g0122 a0001c0002t0035g0123 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.61-1758A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249371 | |||||||
| chr12:69249377 | T | A | 1 | a0001c0001t0030g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.61-1752T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249377 | |||||||
| chr12:69249426 | T | TTC | 258 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(255): Show |
388 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(385): Show |
intron_variant | MODIFIER | c.61-1701_61-1700dup others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69249426 | ||||||
| chr12:69249495 | G | C | 4 | a0001c0001t0031g0170 a0001c0001t0031g0204 a0001c0001t0065g0156 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-1634G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249495 | |||||||
| chr12:69249541 | C | T | 139 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(136): Show |
227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.61-1588C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249541 | |||||||
| chr12:69249747 | G | A | 6 | a0001c0002t0012g0007 a0001c0002t0012g0088 a0001c0002t0036g0016 others(3): Show |
12 | HG01361.hp2 HG01884.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-1382G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249747 | |||||||
| chr12:69249809 | A | G | 1 | a0001c0002t0001g0121 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.61-1320A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69249809 | |||||||
| chr12:69250030 | A | G | 1 | a0001c0001t0027g0051 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61-1099A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250030 | |||||||
| chr12:69250099 | CATTT | C | 3 | a0001c0001t0077g0017 a0001c0001t0078g0017 a0001c0001t0079g0017 |
3 | HG00639.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.61-1026_61-1023del others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250099 | ||||||
| chr12:69250109 | G | A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0121 |
2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.61-1020G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250109 | |||||||
| chr12:69250171 | T | C | 1 | a0001c0001t0085g0085 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61-958T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250171 | |||||||
| chr12:69250205 | A | T | 6 | a0001c0001t0031g0170 a0001c0001t0031g0204 a0001c0001t0033g0147 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-924A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250205 | |||||||
| chr12:69250271 | G | A | 31 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(28): Show |
42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.61-858G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250271 | |||||||
| chr12:69250416 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61-713C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250416 | |||||||
| chr12:69250483 | G | A | 1 | a0001c0001t0003g0072 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.61-646G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250483 | |||||||
| chr12:69250520 | G | A | 4 | a0001c0002t0001g0012 a0001c0002t0001g0098 a0001c0002t0048g0012 others(1): Show |
6 | NA18947.hp1 NA18954.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-609G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250520 | |||||||
| chr12:69250561 | G | A | 1 | a0001c0001t0027g0051 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61-568G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250561 | |||||||
| chr12:69250590 | C | CA | 17 | a0001c0001t0002g0045 a0001c0001t0002g0054 a0001c0001t0002g0056 others(14): Show |
18 | HG00639.hp2 HG00741.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.61-522dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250590 | ||||||
| chr12:69250590 | CA | C | 27 | a0001c0001t0013g0046 a0001c0001t0013g0058 a0001c0001t0013g0182 others(24): Show |
28 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.61-522delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250590 | ||||||
| chr12:69250603 | A | G | 6 | a0001c0001t0014g0207 a0001c0001t0014g0209 a0001c0001t0019g0025 others(3): Show |
7 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.61-526A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250603 | |||||||
| chr12:69250608 | GAAAA | G | 86 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0006 others(83): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.61-516_61-513delAA others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250608 | ||||||
| chr12:69250612 | A | G | 4 | a0001c0002t0001g0038 a0001c0002t0001g0039 a0001c0002t0025g0038 others(1): Show |
5 | HG01433.hp2 HG01981.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-517A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250612 | |||||||
| chr12:69250655 | G | T | 1 | a0001c0001t0002g0201 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.61-474G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250655 | |||||||
| chr12:69250655 | GT | G | 189 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(186): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.61-465delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 69250655 | ||||||
| chr12:69250831 | G | A | 3 | a0001c0001t0002g0044 a0001c0001t0002g0158 a0001c0001t0002g0167 |
4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-298G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69250831 | |||||||
| chr12:69251023 | C | T | 1 | a0001c0001t0027g0051 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61-106C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 1/9 | chr12 | 69251023 | |||||||
| chr12:69251401 | A | C | 1 | a0001c0001t0052g0162 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.270+63A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251401 | |||||||
| chr12:69251449 | A | G | 2 | a0001c0001t0019g0025 a0001c0001t0050g0025 |
3 | HG01167.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.270+111A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251449 | |||||||
| chr12:69251455 | G | T | 40 | a0001c0002t0001g0003 a0001c0002t0001g0012 a0001c0002t0001g0019 others(37): Show |
54 | HG00408.hp2 HG00673.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.270+117G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251455 | |||||||
| chr12:69251459 | G | T | 1 | a0001c0001t0020g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.270+121G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251459 | |||||||
| chr12:69251605 | T | C | 9 | a0001c0001t0013g0046 a0001c0001t0013g0058 a0001c0001t0013g0182 others(6): Show |
9 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+267T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251605 | |||||||
| chr12:69251786 | T | C | 31 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(28): Show |
42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.270+448T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251786 | |||||||
| chr12:69251818 | C | T | 43 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(40): Show |
69 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.270+480C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251818 | |||||||
| chr12:69251960 | A | G | 1 | a0001c0004t0013g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.270+622A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69251960 | |||||||
| chr12:69252059 | C | CG | 3 | a0001c0002t0012g0007 a0001c0002t0012g0088 a0001c0002t0072g0007 |
7 | HG01361.hp2 HG01884.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+722dupG | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 69252059 | ||||||
| chr12:69252083 | C | T | 2 | a0001c0001t0032g0145 a0001c0001t0032g0146 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.270+745C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252083 | |||||||
| chr12:69252084 | A | G | 193 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(190): Show |
294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.270+746A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252084 | |||||||
| chr12:69252140 | T | A | 1 | a0001c0001t0064g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.270+802T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252140 | |||||||
| chr12:69252143 | T | C | 1 | a0001c0002t0001g0100 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.270+805T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252143 | |||||||
| chr12:69252230 | T | C | 193 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(190): Show |
294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.271-821T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252230 | |||||||
| chr12:69252253 | C | CAAAA | 185 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(182): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.271-795_271-794ins others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 69252253 | ||||||
| chr12:69252253 | C | CAAAAA | 8 | a0001c0001t0013g0046 a0001c0001t0013g0058 a0001c0001t0013g0182 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-795_271-794ins others(5): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 69252253 | ||||||
| chr12:69252377 | A | G | 7 | a0001c0001t0014g0207 a0001c0001t0014g0209 a0001c0001t0019g0025 others(4): Show |
8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-674A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252377 | |||||||
| chr12:69252537 | G | A | 1 | a0001c0001t0002g0199 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.271-514G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252537 | |||||||
| chr12:69252568 | T | C | 1 | a0001c0001t0027g0051 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.271-483T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252568 | |||||||
| chr12:69252631 | A | G | 2 | a0001c0001t0003g0026 a0001c0001t0040g0082 |
3 | NA18960.hp1 NA18963.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.271-420A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252631 | |||||||
| chr12:69252912 | C | G | 8 | a0001c0001t0013g0046 a0001c0001t0013g0058 a0001c0001t0013g0182 others(5): Show |
8 | HG02055.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-139C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 2/9 | chr12 | 69252912 | |||||||
| chr12:69253340 | C | G | 1 | a0001c0001t0063g0063 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.374+186C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253340 | |||||||
| chr12:69253362 | G | C | 3 | a0001c0001t0007g0133 a0001c0001t0007g0134 a0001c0001t0007g0135 |
3 | HG02027.hp1 HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.374+208G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253362 | |||||||
| chr12:69253461 | C | A | 3 | a0001c0001t0002g0014 a0001c0003t0002g0014 a0001c0003t0038g0014 |
4 | HG00558.hp2 NA18975.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.374+307C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253461 | |||||||
| chr12:69253498 | A | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.374+344A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253498 | |||||||
| chr12:69253575 | A | G | 2 | a0001c0001t0033g0147 a0001c0001t0033g0148 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.374+421A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253575 | |||||||
| chr12:69253710 | A | G | 1 | a0001c0002t0001g0109 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.374+556A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253710 | |||||||
| chr12:69253900 | T | C | 1 | a0001c0002t0001g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.374+746T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69253900 | |||||||
| chr12:69254176 | G | C | 1 | a0001c0001t0086g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.374+1022G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254176 | |||||||
| chr12:69254182 | C | T | 139 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(136): Show |
227 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.374+1028C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254182 | |||||||
| chr12:69254183 | T | TA | 82 | a0001c0001t0014g0207 a0001c0001t0014g0209 a0001c0001t0019g0025 others(79): Show |
129 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.374+1039dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 69254183 | ||||||
| chr12:69254183 | TA | T | 29 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(26): Show |
40 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.374+1039delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 69254183 | ||||||
| chr12:69254184 | A | T | 6 | a0001c0002t0001g0006 a0001c0002t0001g0018 a0001c0002t0001g0067 others(3): Show |
14 | HG01069.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.374+1030A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254184 | |||||||
| chr12:69254185 | A | T | 1 | a0001c0002t0001g0092 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.374+1031A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254185 | |||||||
| chr12:69254301 | A | C | 2 | a0001c0001t0029g0178 a0001c0001t0029g0179 |
2 | HG00738.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.374+1147A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254301 | |||||||
| chr12:69254466 | A | G | 31 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(28): Show |
42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.374+1312A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254466 | |||||||
| chr12:69254548 | C | T | 31 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(28): Show |
42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.374+1394C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254548 | |||||||
| chr12:69254574 | G | A | 1 | a0001c0001t0047g0186 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.374+1420G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254574 | |||||||
| chr12:69254631 | G | A | 2 | a0001c0001t0033g0147 a0001c0001t0033g0148 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.374+1477G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254631 | |||||||
| chr12:69254946 | A | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.375-1751A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69254946 | |||||||
| chr12:69255367 | A | T | 2 | a0001c0002t0036g0016 a0001c0002t0071g0016 |
3 | HG02451.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.375-1330A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255367 | |||||||
| chr12:69255432 | A | G | 6 | a0001c0002t0012g0007 a0001c0002t0012g0088 a0001c0002t0036g0016 others(3): Show |
12 | HG01361.hp2 HG01884.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.375-1265A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255432 | |||||||
| chr12:69255535 | A | G | 6 | a0001c0002t0012g0007 a0001c0002t0012g0088 a0001c0002t0036g0016 others(3): Show |
12 | HG01361.hp2 HG01884.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.375-1162A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255535 | |||||||
| chr12:69255606 | A | T | 1 | a0001c0001t0015g0081 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.375-1091A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255606 | |||||||
| chr12:69255661 | C | A | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.375-1036C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255661 | |||||||
| chr12:69255723 | G | C | 1 | a0001c0002t0006g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.375-974G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255723 | |||||||
| chr12:69255790 | G | GC | 3 | a0001c0002t0012g0007 a0001c0002t0012g0088 a0001c0002t0072g0007 |
7 | HG01361.hp2 HG01884.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.375-905dupC | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 69255790 | ||||||
| chr12:69255807 | G | A | 2 | a0001c0001t0013g0058 a0001c0001t0021g0059 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.375-890G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255807 | |||||||
| chr12:69255838 | C | T | 15 | a0001c0001t0020g0140 a0001c0001t0020g0141 a0001c0001t0030g0138 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.375-859C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255838 | |||||||
| chr12:69255870 | T | C | 1 | a0001c0002t0001g0096 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.375-827T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69255870 | |||||||
| chr12:69256122 | A | T | 1 | a0001c0001t0031g0170 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.375-575A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256122 | |||||||
| chr12:69256134 | A | G | 1 | a0001c0001t0028g0047 | 2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.375-563A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256134 | |||||||
| chr12:69256343 | A | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.375-354A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256343 | |||||||
| chr12:69256356 | C | T | 1 | a0001c0001t0008g0080 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.375-341C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256356 | |||||||
| chr12:69256370 | A | G | 1 | a0001c0001t0003g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.375-327A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 3/9 | chr12 | 69256370 | |||||||
| chr12:69257048 | T | C | 1 | a0001c0002t0004g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.520+206T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257048 | |||||||
| chr12:69257180 | A | G | 1 | a0001c0002t0069g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.520+338A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257180 | |||||||
| chr12:69257244 | A | G | 1 | a0001c0001t0004g0078 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.520+402A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257244 | |||||||
| chr12:69257301 | G | C | 2 | a0001c0001t0020g0140 a0001c0001t0020g0141 |
2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.521-431G>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257301 | |||||||
| chr12:69257396 | A | T | 5 | a0001c0001t0013g0046 a0001c0001t0013g0182 a0001c0001t0020g0180 others(2): Show |
5 | HG02055.hp1 HG02818.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.521-336A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257396 | |||||||
| chr12:69257397 | C | T | 4 | a0001c0001t0031g0170 a0001c0001t0031g0204 a0001c0001t0065g0156 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.521-335C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257397 | |||||||
| chr12:69257405 | G | A | 1 | a0001c0001t0027g0051 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.521-327G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257405 | |||||||
| chr12:69257413 | C | A | 2 | a0001c0001t0019g0050 a0001c0001t0049g0050 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.521-319C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257413 | |||||||
| chr12:69257416 | A | C | 15 | a0001c0001t0020g0140 a0001c0001t0020g0141 a0001c0001t0030g0138 others(12): Show |
15 | HG02109.hp2 HG02572.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.521-316A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 4/9 | chr12 | 69257416 | |||||||
| chr12:69257920 | A | G | 1 | a0001c0002t0001g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.694+15A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | chr12 | 69257920 | |||||||
| chr12:69258358 | T | C | 2 | a0001c0001t0065g0156 a0001c0001t0066g0143 |
2 | HG02109.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.695-232T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | chr12 | 69258358 | |||||||
| chr12:69258434 | T | C | 1 | a0001c0002t0001g0052 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.695-156T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | chr12 | 69258434 | |||||||
| chr12:69258435 | G | A | 1 | a0001c0002t0068g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.695-155G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | chr12 | 69258435 | |||||||
| chr12:69258556 | G | GT | 191 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(188): Show |
292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.695-25dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 69258556 | ||||||
| chr12:69259104 | T | C | 1 | a0001c0001t0043g0028 | 2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1199+10T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/9 | chr12 | 69259104 | |||||||
| chr12:69259292 | A | C | 1 | a0001c0001t0009g0169 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1200-136A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/9 | chr12 | 69259292 | |||||||
| chr12:69259366 | T | C | 140 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(137): Show |
228 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1200-62T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 6/9 | chr12 | 69259366 | |||||||
| chr12:69259600 | A | G | 7 | a0001c0001t0020g0140 a0001c0001t0020g0141 a0001c0001t0030g0138 others(4): Show |
7 | HG02723.hp2 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1315+57A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259600 | |||||||
| chr12:69259608 | T | C | 1 | a0001c0001t0051g0137 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1315+65T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259608 | |||||||
| chr12:69259732 | A | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0161 |
2 | NA18986.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1315+189A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259732 | |||||||
| chr12:69259749 | A | T | 1 | a0001c0002t0006g0130 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1315+206A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259749 | |||||||
| chr12:69259906 | A | G | 6 | a0001c0001t0020g0140 a0001c0001t0020g0141 a0001c0001t0030g0138 others(3): Show |
6 | HG02723.hp2 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316-138A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259906 | |||||||
| chr12:69259996 | T | G | 5 | a0001c0002t0001g0012 a0001c0002t0001g0098 a0001c0002t0001g0116 others(2): Show |
7 | NA18947.hp1 NA18954.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1316-48T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 7/9 | chr12 | 69259996 | |||||||
| chr12:69260287 | T | A | 1 | a0001c0001t0009g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1469+90T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260287 | |||||||
| chr12:69260319 | G | GT | 61 | a0001c0001t0002g0044 a0001c0001t0002g0154 a0001c0001t0002g0158 others(58): Show |
92 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1469+133dupT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69260319 | ||||||
| chr12:69260319 | G | GTT | 87 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0006 others(84): Show |
147 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1469+132_1469+133d others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69260319 | ||||||
| chr12:69260323 | T | G | 1 | a0001c0001t0028g0047 | 2 | HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1469+126T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260323 | |||||||
| chr12:69260335 | C | A | 1 | a0001c0001t0065g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1469+138C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260335 | |||||||
| chr12:69260336 | T | G | 1 | a0001c0001t0065g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1469+139T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260336 | |||||||
| chr12:69260407 | A | G | 91 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0006 others(88): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1469+210A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260407 | |||||||
| chr12:69260526 | T | C | 6 | a0001c0001t0014g0207 a0001c0001t0014g0209 a0001c0001t0019g0025 others(3): Show |
7 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469+329T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260526 | |||||||
| chr12:69260560 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1469+363G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260560 | |||||||
| chr12:69260607 | C | T | 1 | a0001c0001t0005g0187 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1469+410C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260607 | |||||||
| chr12:69260656 | G | A | 1 | a0001c0002t0001g0037 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1469+459G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69260656 | |||||||
| chr12:69261038 | T | C | 1 | a0001c0001t0003g0074 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1469+841T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261038 | |||||||
| chr12:69261179 | C | T | 6 | a0001c0001t0020g0140 a0001c0001t0020g0141 a0001c0001t0030g0138 others(3): Show |
6 | HG02723.hp2 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469+982C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261179 | |||||||
| chr12:69261186 | C | A | 1 | a0001c0001t0064g0193 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1469+989C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261186 | |||||||
| chr12:69261275 | CT | C | 2 | a0001c0002t0036g0016 a0001c0002t0071g0016 |
3 | HG02451.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1469+1083delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69261275 | ||||||
| chr12:69261336 | G | A | 2 | a0001c0001t0013g0182 a0001c0001t0021g0181 |
2 | HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1470-1037G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261336 | |||||||
| chr12:69261387 | A | G | 177 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(174): Show |
278 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.1470-986A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261387 | |||||||
| chr12:69261434 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1470-939G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261434 | |||||||
| chr12:69261500 | G | GGATGAAA others(62): Show |
2 | a0001c0004t0013g0173 a0001c0004t0013g0197 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1470-872_1470-804d others(71): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69261500 | ||||||
| chr12:69261596 | G | A | 1 | a0001c0002t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1470-777G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261596 | |||||||
| chr12:69261664 | T | G | 2 | a0001c0001t0011g0043 a0001c0001t0011g0165 |
3 | HG00639.hp2 HG00741.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1470-709T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261664 | |||||||
| chr12:69261852 | C | T | 2 | a0001c0001t0019g0050 a0001c0001t0049g0050 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1470-521C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69261852 | |||||||
| chr12:69262122 | T | TA | 138 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(135): Show |
226 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.1470-249dupA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 69262122 | ||||||
| chr12:69262320 | T | C | 1 | a0001c0001t0015g0075 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1470-53T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69262320 | |||||||
| chr12:69262322 | T | G | 2 | a0001c0002t0006g0041 a0001c0002t0006g0126 |
3 | NA18959.hp1 NA18964.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1470-51T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 8/9 | chr12 | 69262322 | |||||||
| chr12:69262985 | A | C | 8 | a0001c0001t0002g0015 a0001c0001t0002g0045 a0001c0001t0002g0132 others(5): Show |
10 | HG00735.hp2 HG02083.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.*3+423A>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69262985 | |||||||
| chr12:69263030 | A | G | 1 | a0001c0001t0002g0042 | 2 | HG01123.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.*3+468A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263030 | |||||||
| chr12:69263096 | AT | A | 190 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(187): Show |
291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.*3+545delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69263096 | ||||||
| chr12:69263098 | T | A | 41 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(38): Show |
67 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.*3+536T>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263098 | |||||||
| chr12:69263365 | G | A | 192 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(189): Show |
293 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.*3+803G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263365 | |||||||
| chr12:69263528 | T | C | 1 | a0001c0002t0001g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*3+966T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263528 | |||||||
| chr12:69263651 | G | A | 1 | a0001c0002t0006g0130 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.*3+1089G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263651 | |||||||
| chr12:69263659 | A | G | 1 | a0001c0001t0059g0064 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.*3+1097A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263659 | |||||||
| chr12:69263947 | C | T | 1 | a0001c0002t0001g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*3+1385C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69263947 | |||||||
| chr12:69264193 | G | A | 2 | a0001c0001t0030g0138 a0001c0001t0030g0139 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.*3+1631G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264193 | |||||||
| chr12:69264371 | A | G | 1 | a0001c0001t0005g0185 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*3+1809A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264371 | |||||||
| chr12:69264381 | T | C | 3 | a0001c0001t0023g0013 a0001c0001t0051g0137 a0001c0001t0070g0013 |
5 | HG00733.hp2 HG01070.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.*3+1819T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264381 | |||||||
| chr12:69264550 | T | C | 77 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0012 others(74): Show |
123 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.*3+1988T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264550 | |||||||
| chr12:69264890 | T | C | 1 | a0001c0001t0002g0024 | 3 | NA18942.hp1 NA18945.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.*3+2328T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264890 | |||||||
| chr12:69264955 | G | A | 1 | a0001c0001t0007g0163 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.*3+2393G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69264955 | |||||||
| chr12:69265090 | T | G | 1 | a0001c0002t0006g0128 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.*3+2528T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265090 | |||||||
| chr12:69265120 | C | G | 1 | a0001c0001t0002g0136 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.*3+2558C>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265120 | |||||||
| chr12:69265175 | C | A | 1 | a0001c0001t0020g0180 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*3+2613C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265175 | |||||||
| chr12:69265193 | A | T | 1 | a0001c0002t0001g0036 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.*3+2631A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265193 | |||||||
| chr12:69265234 | G | A | 1 | a0001c0001t0027g0051 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*3+2672G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265234 | |||||||
| chr12:69265519 | A | G | 77 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0012 others(74): Show |
123 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.*3+2957A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265519 | |||||||
| chr12:69265589 | A | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(39): Show |
68 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.*3+3027A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265589 | |||||||
| chr12:69265598 | CT | C | 132 | a0001c0001t0002g0158 a0001c0001t0003g0002 a0001c0001t0003g0026 others(129): Show |
214 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.*3+3057delT | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69265598 | ||||||
| chr12:69265598 | CTT | C | 51 | a0001c0001t0003g0031 a0001c0001t0003g0086 a0001c0001t0003g0174 others(48): Show |
64 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.*3+3056_*3+3057del others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69265598 | ||||||
| chr12:69265598 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0007g0164 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.*3+3048_*3+3057del others(10): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69265598 | ||||||
| chr12:69265657 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.*3+3095C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265657 | |||||||
| chr12:69265832 | C | A | 1 | a0001c0005t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.*3+3270C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265832 | |||||||
| chr12:69265896 | G | A | 1 | a0001c0001t0005g0184 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.*3+3334G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265896 | |||||||
| chr12:69265898 | G | A | 31 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(28): Show |
42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.*3+3336G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69265898 | |||||||
| chr12:69266026 | T | TG | 5 | a0001c0001t0031g0170 a0001c0001t0031g0204 a0001c0001t0033g0148 others(2): Show |
5 | HG02109.hp2 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.*3+3465dupG | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69266026 | ||||||
| chr12:69266027 | GA | G | 47 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(44): Show |
74 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.*4-3470delA | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69266027 | ||||||
| chr12:69266027 | GAAAA | G | 94 | a0001c0001t0023g0013 a0001c0001t0051g0137 a0001c0001t0070g0013 others(91): Show |
156 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.*4-3473_*4-3470del others(4): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69266027 | ||||||
| chr12:69266032 | A | G | 1 | a0001c0002t0009g0095 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*3+3470A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266032 | |||||||
| chr12:69266064 | C | A | 1 | a0001c0002t0001g0018 | 3 | HG02647.hp2 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.*4-3448C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266064 | |||||||
| chr12:69266140 | C | A | 7 | a0001c0001t0014g0207 a0001c0001t0014g0209 a0001c0001t0019g0025 others(4): Show |
8 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.*4-3372C>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266140 | |||||||
| chr12:69266200 | T | TCTGAGGT others(20): Show |
1 | a0001c0001t0014g0207 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*4-3308_*4-3282dup others(27): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69266200 | ||||||
| chr12:69266358 | T | C | 1 | a0001c0001t0060g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.*4-3154T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266358 | |||||||
| chr12:69266604 | C | T | 1 | a0001c0001t0022g0168 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.*4-2908C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266604 | |||||||
| chr12:69266765 | T | G | 1 | a0001c0001t0005g0183 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.*4-2747T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266765 | |||||||
| chr12:69266923 | T | C | 17 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(14): Show |
28 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.*4-2589T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266923 | |||||||
| chr12:69266951 | T | G | 2 | a0001c0001t0033g0147 a0001c0001t0033g0148 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.*4-2561T>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69266951 | |||||||
| chr12:69267036 | A | G | 2 | a0001c0001t0013g0058 a0001c0001t0021g0059 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*4-2476A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267036 | |||||||
| chr12:69267099 | G | T | 1 | a0001c0002t0001g0113 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*4-2413G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267099 | |||||||
| chr12:69267351 | A | G | 138 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(135): Show |
226 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.*4-2161A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267351 | |||||||
| chr12:69267404 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.*4-2108T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267404 | |||||||
| chr12:69267647 | C | T | 2 | a0001c0001t0019g0025 a0001c0001t0050g0025 |
3 | HG01167.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.*4-1865C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267647 | |||||||
| chr12:69267789 | A | G | 1 | a0001c0002t0001g0037 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.*4-1723A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267789 | |||||||
| chr12:69267810 | T | C | 1 | a0001c0001t0053g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*4-1702T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267810 | |||||||
| chr12:69267933 | G | A | 1 | a0001c0001t0032g0145 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.*4-1579G>A | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69267933 | |||||||
| chr12:69268038 | G | T | 1 | a0001c0001t0013g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*4-1474G>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69268038 | |||||||
| chr12:69268107 | T | C | 4 | a0001c0001t0019g0025 a0001c0001t0019g0050 a0001c0001t0049g0050 others(1): Show |
5 | HG01167.hp2 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.*4-1405T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69268107 | |||||||
| chr12:69268476 | ACT | A | 41 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(38): Show |
67 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.*4-1033_*4-1032del others(2): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69268476 | ||||||
| chr12:69268581 | CCTTCTGC others(3): Show |
C | 1 | a0001c0002t0001g0116 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.*4-927_*4-918delCT others(8): Show |
CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 69268581 | ||||||
| chr12:69268714 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.*4-798A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69268714 | |||||||
| chr12:69269074 | T | C | 2 | a0001c0002t0036g0016 a0001c0002t0071g0016 |
3 | HG02451.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*4-438T>C | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269074 | |||||||
| chr12:69269149 | A | T | 192 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0030 others(189): Show |
293 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.*4-363A>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269149 | |||||||
| chr12:69269267 | C | T | 31 | a0001c0001t0005g0005 a0001c0001t0005g0022 a0001c0001t0005g0023 others(28): Show |
42 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.*4-245C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269267 | |||||||
| chr12:69269350 | A | G | 1 | a0001c0002t0001g0112 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*4-162A>G | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269350 | |||||||
| chr12:69269351 | C | T | 2 | a0001c0002t0001g0094 a0001c0002t0001g0121 |
2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.*4-161C>T | CPSF6 | ENSG00000111605.18 | transcript | ENST00000435070.7 | protein_coding | 9/9 | chr12 | 69269351 |