Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9125 |
| ensemblid | ENSG00000144580.15 |
| hgncid | 10445 |
| symbol | CNOT9 |
| name | CCR4-NOT transcription complex subunit 9 |
| refseq_nuc | NM_005444.3 |
| refseq_prot | NP_005435.1 |
| ensembl_nuc | ENST00000273064.11 |
| ensembl_prot | ENSP00000273064.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 218568839 |
| end | 218597080 |
| strand | + |
| ver | v1.2 |
| region | chr2:218568839-218597080 |
| region5000 | chr2:218563839-218602080 |
| regionname0 | CNOT9_chr2_218568839_218597080 |
| regionname5000 | CNOT9_chr2_218563839_218602080 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 897 | 322 | 88 | 42 | 136 | 12 | 42 | CNOT9_chr2_218563839_218602080 | CNOT9 | ATGCA others(892): Show |
chr2 | 218563839 | 218602080 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3817 | 55 | 7 | 15 | 17 | 5 | 11 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3812): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0002 | 0/1 | 3824 | 54 | 3 | 5 | 34 | 2 | 9 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3819): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0003 | 0/0 | 3825 | 46 | 4 | 10 | 19 | 2 | 11 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3820): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0004 | 0/0 | 3820 | 36 | 3 | 0 | 31 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3815): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0005 | 0/0 | 3826 | 14 | 3 | 3 | 5 | 1 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3821): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0006 | 0/0 | 3803 | 12 | 12 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3798): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0007 | 0/0 | 3818 | 9 | 2 | 2 | 4 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3813): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0008 | 0/0 | 3827 | 8 | 0 | 2 | 3 | 1 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3822): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0009 | 0/0 | 3820 | 6 | 6 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3815): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0010 | 0/0 | 3821 | 6 | 1 | 0 | 5 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3816): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0011 | 1/0 | 3820 | 6 | 1 | 2 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3815): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0012 | 0/0 | 3824 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3819): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0013 | 0/0 | 3821 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3816): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0014 | 0/0 | 3817 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3812): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0015 | 0/0 | 3822 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3817): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0016 | 0/0 | 3823 | 3 | 1 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3818): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0017 | 0/0 | 3817 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3812): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0018 | 0/0 | 3823 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3818): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0019 | 0/0 | 3816 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3811): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0020 | 0/0 | 3819 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3814): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0021 | 0/0 | 3825 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3820): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0022 | 0/0 | 3830 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3825): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0023 | 0/0 | 3821 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3816): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0024 | 0/0 | 3824 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3819): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0025 | 0/0 | 3824 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3819): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0026 | 0/0 | 3803 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3798): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0027 | 0/0 | 3820 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3815): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0028 | 0/0 | 3824 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3819): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0029 | 0/0 | 3826 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3821): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0030 | 0/0 | 3818 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3813): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0031 | 0/0 | 3824 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3819): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0032 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3820): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0033 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3820): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0034 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3820): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0035 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3820): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0036 | 0/0 | 3828 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3823): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0037 | 0/0 | 3826 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3821): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0038 | 0/0 | 3820 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3815): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0039 | 0/0 | 3827 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3822): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0040 | 0/0 | 3831 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3826): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0041 | 0/0 | 3831 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3826): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0042 | 0/0 | 3822 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3817): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0043 | 0/0 | 3819 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3814): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0044 | 0/0 | 3820 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3815): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0045 | 0/0 | 3824 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3819): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0046 | 0/0 | 3818 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3813): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0047 | 0/0 | 3819 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3814): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0048 | 0/0 | 3820 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3815): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0049 | 0/0 | 3823 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3818): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0050 | 0/0 | 3817 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3812): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0051 | 0/0 | 3805 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3800): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0052 | 0/0 | 3818 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3813): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0053 | 0/0 | 3819 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3814): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0054 | 0/0 | 3826 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3821): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0055 | 0/0 | 3824 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3819): Show |
chr2 | 218563839 | 218602080 |
| a0001c0001t0056 | 0/0 | 3817 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | GAGCC others(3812): Show |
chr2 | 218563839 | 218602080 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 0 | 8 | 9 | 2 | 9 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0002 | 0/0 | 11 | 0 | 2 | 8 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0002 | 0/0 | 8 | 0 | 3 | 4 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0004 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0007 | 0/0 | 5 | 3 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0006g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0006g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0008g0002 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0010g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0010g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0011g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0011g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0011g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0012g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0013g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0013g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0013g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0013g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0014g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0014g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0015g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0015g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0016g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0016g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0016g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0017g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0018g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0018g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0019g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0019g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0020g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0020g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0021g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0022g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0022g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0023g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0024g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0024g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0025g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0026g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0027g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0028g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0029g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0030g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0031g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0032g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0033g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0034g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0035g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0036g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0037g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0038g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0039g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0040g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0041g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0042g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0043g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0044g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0045g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0046g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0047g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0048g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0049g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0050g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0051g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0052g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0053g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0054g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0055g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| a0001c0001t0056g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0056 | g0107 | EUR | GBR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0064 | EUR | GBR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0051 | EUR | FIN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | FIN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00673 | hp1 | a0001 | c0001 | t0016 | g0078 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00673 | hp2 | a0001 | c0001 | t0016 | g0059 | EAS | CHS | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01070 | hp2 | a0001 | c0001 | t0011 | g0015 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01081 | hp1 | a0001 | c0001 | t0011 | g0001 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01081 | hp2 | a0001 | c0001 | t0045 | g0088 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01109 | hp1 | a0001 | c0001 | t0042 | g0162 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01884 | hp2 | a0001 | c0001 | t0040 | g0018 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01975 | hp1 | a0001 | c0001 | t0024 | g0103 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02015 | hp1 | a0001 | c0001 | t0035 | g0057 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02015 | hp2 | a0001 | c0001 | t0021 | g0012 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0063 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02055 | hp1 | a0001 | c0001 | t0041 | g0155 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02071 | hp2 | a0001 | c0001 | t0021 | g0012 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02074 | hp2 | a0001 | c0001 | t0010 | g0171 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0113 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | KHV | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02145 | hp2 | a0001 | c0001 | t0052 | g0030 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02155 | hp1 | a0001 | c0001 | t0029 | g0002 | EAS | CDX | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | CDX | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0033 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02257 | hp2 | a0001 | c0001 | t0044 | g0154 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0149 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0188 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02451 | hp2 | a0001 | c0001 | t0043 | g0163 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02572 | hp1 | a0001 | c0001 | t0022 | g0018 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0009 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02622 | hp1 | a0001 | c0001 | t0030 | g0009 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0142 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02630 | hp2 | a0001 | c0001 | t0053 | g0133 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0151 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0008 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0125 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0090 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02818 | hp1 | a0001 | c0001 | t0027 | g0018 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02886 | hp1 | a0001 | c0001 | t0023 | g0031 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0008 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02896 | hp2 | a0001 | c0001 | t0018 | g0126 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0129 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0130 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0005 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0159 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02976 | hp2 | a0001 | c0001 | t0046 | g0178 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03041 | hp2 | a0001 | c0001 | t0038 | g0150 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03098 | hp1 | a0001 | c0001 | t0024 | g0128 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0136 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0148 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03195 | hp1 | a0001 | c0001 | t0054 | g0105 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03195 | hp2 | a0001 | c0001 | t0019 | g0144 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03209 | hp1 | a0001 | c0001 | t0019 | g0143 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03239 | hp2 | a0001 | c0001 | t0036 | g0100 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03453 | hp1 | a0001 | c0001 | t0023 | g0031 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03453 | hp2 | a0001 | c0001 | t0022 | g0161 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0127 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03516 | hp2 | a0001 | c0001 | t0016 | g0140 | AFR | ESN | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0032 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0179 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03579 | hp2 | a0001 | c0001 | t0020 | g0009 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0026 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03654 | hp2 | a0001 | c0001 | t0047 | g0006 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0026 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03688 | hp2 | a0001 | c0001 | t0049 | g0180 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0002 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG04184 | hp2 | a0001 | c0001 | t0007 | g0029 | SAS | BEB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG04199 | hp2 | a0001 | c0001 | t0008 | g0002 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG04228 | hp1 | a0001 | c0001 | t0050 | g0119 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | YRI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | YRI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | CHB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18959 | hp1 | a0001 | c0001 | t0025 | g0098 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18963 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18964 | hp2 | a0001 | c0001 | t0037 | g0020 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18967 | hp2 | a0001 | c0001 | t0008 | g0096 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18968 | hp2 | a0001 | c0001 | t0033 | g0047 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18971 | hp2 | a0001 | c0001 | t0031 | g0074 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18977 | hp1 | a0001 | c0001 | t0028 | g0077 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18978 | hp1 | a0001 | c0001 | t0051 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18981 | hp2 | a0001 | c0001 | t0039 | g0012 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18984 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19002 | hp2 | a0001 | c0001 | t0034 | g0020 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19011 | hp2 | a0001 | c0001 | t0010 | g0182 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19012 | hp1 | a0001 | c0001 | t0010 | g0177 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0065 | AFR | LWK | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19056 | hp1 | a0001 | c0001 | t0048 | g0184 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19056 | hp2 | a0001 | c0001 | t0032 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19077 | hp1 | a0001 | c0001 | t0008 | g0060 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19078 | hp2 | a0001 | c0001 | t0007 | g0109 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19081 | hp2 | a0001 | c0001 | t0010 | g0166 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19089 | hp2 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0118 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19240 | hp1 | a0001 | c0001 | t0015 | g0138 | AFR | YRI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | YRI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0131 | AFR | ASW | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20129 | hp2 | a0001 | c0001 | t0015 | g0137 | AFR | ASW | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0085 | EUR | TSI | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0186 | SAS | GIH | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0030 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0139 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02109 | hp2 | a0001 | c0001 | t0017 | g0005 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02486 | hp2 | a0001 | c0001 | t0014 | g0152 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02559 | hp1 | a0001 | c0001 | t0026 | g0153 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03471 | hp1 | a0001 | c0001 | t0017 | g0005 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG03471 | hp2 | a0001 | c0001 | t0055 | g0104 | AFR | MSL | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG06807 | hp1 | a0001 | c0001 | t0014 | g0009 | AFR | USA | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0033 | AFR | USA | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | USA | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0032 | AFR | USA | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | LWK | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0069 | AFR | LWK | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0052 | REF | REF | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0011 | g0132 | REF | REF | CNOT9_chr2_218563839_218602080 | CNOT9 | chr2 | 218563839 | 218602080 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218568874 | G | A | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(38): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
5_prime_UTR_variant | MODIFIER | c.-81G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/8 | 81 | chr2 | 218568874 | ||||||
| chr2:218594723 | C | A | 1 | a0001c0001t0025 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 447 | chr2 | 218594723 | ||||||
| chr2:218594741 | G | C | 1 | a0001c0001t0050 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 465 | chr2 | 218594741 | ||||||
| chr2:218594982 | A | G | 7 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0012 others(4): Show |
51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*706A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 706 | chr2 | 218594982 | ||||||
| chr2:218595214 | A | G | 1 | a0001c0001t0045 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*938A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 938 | chr2 | 218595214 | ||||||
| chr2:218595216 | A | T | 1 | a0001c0001t0013 | 5 | HG02897.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*940A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 940 | chr2 | 218595216 | ||||||
| chr2:218595310 | C | T | 2 | a0001c0001t0043 a0001c0001t0044 |
2 | HG02257.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1034C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1034 | chr2 | 218595310 | ||||||
| chr2:218595330 | A | C | 1 | a0001c0001t0056 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1054A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1054 | chr2 | 218595330 | ||||||
| chr2:218595336 | G | T | 1 | a0001c0001t0042 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1060G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1060 | chr2 | 218595336 | ||||||
| chr2:218595404 | C | CTT | 4 | a0001c0001t0015 a0001c0001t0019 a0001c0001t0054 others(1): Show |
7 | HG03195.hp1 HG03195.hp2 HG03209.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1155_*1156dupTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | C | CTTT | 2 | a0001c0001t0014 a0001c0001t0016 |
7 | HG00673.hp1 HG00673.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1154_*1156dupTTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | C | CTTTT | 7 | a0001c0001t0002 a0001c0001t0025 a0001c0001t0028 others(4): Show |
59 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1153_*1156dupTTTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | C | CTTTTT | 7 | a0001c0001t0003 a0001c0001t0020 a0001c0001t0021 others(4): Show |
54 | HG00438.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1152_*1156dupTTTT others(1): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | C | CTTTTTT | 4 | a0001c0001t0005 a0001c0001t0036 a0001c0001t0037 others(1): Show |
17 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1151_*1156dupTTTT others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | C | CTTTTTTT | 2 | a0001c0001t0008 a0001c0001t0039 |
9 | HG00280.hp2 HG01256.hp2 HG01258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1150_*1156dupTTTT others(3): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0022 | 2 | HG02572.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1147_*1156dupTTTT others(6): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0040 a0001c0001t0041 |
2 | HG01884.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1146_*1156dupTTTT others(7): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1157 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | CT | C | 8 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0018 others(5): Show |
50 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1156delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1156 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | CTT | C | 3 | a0001c0001t0007 a0001c0001t0046 a0001c0001t0052 |
11 | HG00741.hp1 HG01123.hp1 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1155_*1156delTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1155 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | CTTT | C | 6 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0017 others(3): Show |
66 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1154_*1156delTTT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1154 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0026 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1146_*1156delTTTT others(7): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1146 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595404 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0006 | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1144_*1156delTTTT others(9): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1144 | INFO_REALIGN_3_PRIME | chr2 | 218595404 | |||||
| chr2:218595469 | GCCGCTAA others(5): Show |
G | 1 | a0001c0001t0051 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1194_*1205delCCGC others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1194 | chr2 | 218595469 | ||||||
| chr2:218595680 | C | T | 1 | a0001c0001t0048 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1404C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1404 | chr2 | 218595680 | ||||||
| chr2:218595701 | C | T | 1 | a0001c0001t0035 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1425C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1425 | chr2 | 218595701 | ||||||
| chr2:218595912 | C | G | 2 | a0001c0001t0017 a0001c0001t0052 |
4 | HG02109.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1636C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1636 | chr2 | 218595912 | ||||||
| chr2:218596098 | G | T | 3 | a0001c0001t0021 a0001c0001t0031 a0001c0001t0039 |
4 | HG02015.hp2 HG02071.hp2 NA18971.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1822G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1822 | chr2 | 218596098 | ||||||
| chr2:218596201 | T | A | 2 | a0001c0001t0028 a0001c0001t0032 |
2 | NA18977.hp1 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1925T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 1925 | chr2 | 218596201 | ||||||
| chr2:218596357 | C | T | 3 | a0001c0001t0022 a0001c0001t0027 a0001c0001t0041 |
4 | HG02055.hp1 HG02572.hp1 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2081C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2081 | chr2 | 218596357 | ||||||
| chr2:218596538 | A | AAC | 7 | a0001c0001t0013 a0001c0001t0023 a0001c0001t0029 others(4): Show |
12 | HG01109.hp1 HG02155.hp1 HG02886.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2284_*2285dupCA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2286 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | |||||
| chr2:218596538 | A | AACAC | 3 | a0001c0001t0018 a0001c0001t0024 a0001c0001t0054 |
6 | HG01975.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2282_*2285dupCACA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2286 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | |||||
| chr2:218596538 | A | AACACAC | 1 | a0001c0001t0012 | 5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2280_*2285dupCACA others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2286 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | |||||
| chr2:218596538 | AACAC | A | 1 | a0001c0001t0006 | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2282_*2285delCACA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2282 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | |||||
| chr2:218596538 | AACACAC | A | 6 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0020 others(3): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2280_*2285delCACA others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2280 | INFO_REALIGN_3_PRIME | chr2 | 218596538 | |||||
| chr2:218596614 | A | G | 1 | a0001c0001t0026 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2338A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2338 | chr2 | 218596614 | ||||||
| chr2:218596736 | C | G | 2 | a0001c0001t0034 a0001c0001t0037 |
2 | NA18964.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2460C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2460 | chr2 | 218596736 | ||||||
| chr2:218596805 | T | G | 1 | a0001c0001t0033 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2529T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2529 | chr2 | 218596805 | ||||||
| chr2:218597036 | A | AG | 5 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0012 others(2): Show |
49 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2765dupG | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 8/8 | 2766 | INFO_REALIGN_3_PRIME | chr2 | 218597036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218569065 | C | G | 1 | a0001c0001t0011g0188 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.24+87C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569065 | |||||||
| chr2:218569073 | T | G | 1 | a0001c0001t0003g0037 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.24+95T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569073 | |||||||
| chr2:218569165 | C | A | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.24+187C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569165 | |||||||
| chr2:218569322 | A | G | 30 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(27): Show |
46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+344A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569322 | |||||||
| chr2:218569341 | C | T | 1 | a0001c0001t0003g0101 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.24+363C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569341 | |||||||
| chr2:218569413 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.24+435T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569413 | |||||||
| chr2:218569471 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(162): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.24+493A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569471 | |||||||
| chr2:218569485 | C | T | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.24+507C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569485 | |||||||
| chr2:218569537 | T | C | 3 | a0001c0001t0024g0103 a0001c0001t0054g0105 a0001c0001t0055g0104 |
3 | HG01975.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.24+559T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569537 | |||||||
| chr2:218569889 | T | C | 3 | a0001c0001t0024g0103 a0001c0001t0054g0105 a0001c0001t0055g0104 |
3 | HG01975.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.24+911T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218569889 | |||||||
| chr2:218570094 | A | G | 3 | a0001c0001t0024g0103 a0001c0001t0054g0105 a0001c0001t0055g0104 |
3 | HG01975.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.24+1116A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218570094 | |||||||
| chr2:218570262 | T | C | 4 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(1): Show |
4 | HG00642.hp2 HG00741.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+1284T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218570262 | |||||||
| chr2:218570565 | G | A | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.24+1587G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218570565 | |||||||
| chr2:218570730 | C | T | 1 | a0001c0001t0036g0100 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.24+1752C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218570730 | |||||||
| chr2:218571119 | C | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(209): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.24+2141C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571119 | |||||||
| chr2:218571203 | T | G | 1 | a0001c0001t0003g0042 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.24+2225T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571203 | |||||||
| chr2:218571278 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(211): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.24+2300C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571278 | |||||||
| chr2:218571574 | C | CT | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(82): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.24+2610dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571574 | ||||||
| chr2:218571574 | C | CTT | 7 | a0001c0001t0002g0025 a0001c0001t0002g0097 a0001c0001t0002g0099 others(4): Show |
9 | HG01261.hp2 HG03490.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.24+2609_24+2610dup others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571574 | ||||||
| chr2:218571574 | CT | C | 4 | a0001c0001t0010g0166 a0001c0001t0012g0008 a0001c0001t0012g0136 others(1): Show |
7 | HG01975.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+2610delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571574 | ||||||
| chr2:218571586 | T | C | 6 | a0001c0001t0009g0033 a0001c0001t0009g0139 a0001c0001t0015g0033 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.24+2608T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571586 | |||||||
| chr2:218571729 | G | A | 30 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(27): Show |
46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.24+2751G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571729 | |||||||
| chr2:218571738 | A | AT | 93 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(90): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.24+2778dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571738 | ||||||
| chr2:218571738 | A | ATT | 49 | a0001c0001t0002g0024 a0001c0001t0002g0089 a0001c0001t0002g0093 others(46): Show |
57 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.24+2777_24+2778dup others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571738 | ||||||
| chr2:218571738 | AT | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(32): Show |
74 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.24+2778delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218571738 | ||||||
| chr2:218571739 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.24+2761T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571739 | |||||||
| chr2:218571816 | C | T | 2 | a0001c0001t0003g0164 a0001c0001t0005g0165 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.24+2838C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218571816 | |||||||
| chr2:218572159 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.24+3181A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572159 | |||||||
| chr2:218572194 | G | A | 8 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0141 others(5): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+3216G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572194 | |||||||
| chr2:218572227 | G | A | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.24+3249G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572227 | |||||||
| chr2:218572249 | A | T | 125 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(122): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.24+3271A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572249 | |||||||
| chr2:218572295 | T | C | 8 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0141 others(5): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+3317T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572295 | |||||||
| chr2:218572520 | A | G | 1 | a0001c0001t0004g0187 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.24+3542A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572520 | |||||||
| chr2:218572592 | C | T | 12 | a0001c0001t0013g0032 a0001c0001t0013g0129 a0001c0001t0013g0130 others(9): Show |
14 | HG01975.hp1 HG02723.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.24+3614C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572592 | |||||||
| chr2:218572753 | T | C | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.24+3775T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572753 | |||||||
| chr2:218572873 | G | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(162): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.24+3895G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572873 | |||||||
| chr2:218572945 | G | C | 2 | a0001c0001t0006g0016 a0001c0001t0006g0141 |
4 | HG02723.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+3967G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218572945 | |||||||
| chr2:218573115 | C | T | 1 | a0001c0001t0012g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.24+4137C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573115 | |||||||
| chr2:218573223 | C | T | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+4245C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573223 | |||||||
| chr2:218573224 | A | C | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.24+4246A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573224 | |||||||
| chr2:218573258 | T | C | 1 | a0001c0001t0023g0031 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.24+4280T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573258 | |||||||
| chr2:218573297 | A | G | 12 | a0001c0001t0013g0032 a0001c0001t0013g0129 a0001c0001t0013g0130 others(9): Show |
14 | HG01975.hp1 HG02723.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.24+4319A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573297 | |||||||
| chr2:218573318 | TA | T | 157 | a0001c0001t0001g0015 a0001c0001t0001g0121 a0001c0001t0001g0122 others(154): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.24+4360delA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218573318 | ||||||
| chr2:218573318 | TAAAAAAA others(1): Show |
T | 8 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0141 others(5): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.24+4353_24+4360del others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218573318 | ||||||
| chr2:218573438 | A | G | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+4460A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573438 | |||||||
| chr2:218573445 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.24+4467G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573445 | |||||||
| chr2:218573543 | A | G | 1 | a0001c0001t0002g0022 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.24+4565A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573543 | |||||||
| chr2:218573627 | TTTTC | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0050 a0001c0001t0003g0019 others(1): Show |
4 | HG00280.hp2 HG01255.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+4653_24+4656del others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218573627 | ||||||
| chr2:218573636 | C | T | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.24+4658C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573636 | |||||||
| chr2:218573722 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.24+4744A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573722 | |||||||
| chr2:218573767 | A | G | 1 | a0001c0001t0004g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.24+4789A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573767 | |||||||
| chr2:218573826 | G | A | 1 | a0001c0001t0041g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.24+4848G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573826 | |||||||
| chr2:218573939 | A | G | 1 | a0001c0001t0006g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.24+4961A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573939 | |||||||
| chr2:218573940 | A | G | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.24+4962A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218573940 | |||||||
| chr2:218574073 | G | A | 1 | a0001c0001t0056g0107 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.24+5095G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574073 | |||||||
| chr2:218574081 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.24+5103C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574081 | |||||||
| chr2:218574116 | A | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(209): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.24+5138A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574116 | |||||||
| chr2:218574592 | G | A | 5 | a0001c0001t0006g0017 a0001c0001t0006g0145 a0001c0001t0006g0146 others(2): Show |
7 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+5614G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574592 | |||||||
| chr2:218574630 | A | G | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.24+5652A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574630 | |||||||
| chr2:218574814 | T | G | 1 | a0001c0001t0014g0142 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25-5747T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574814 | |||||||
| chr2:218574915 | G | A | 1 | a0001c0001t0006g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.25-5646G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574915 | |||||||
| chr2:218574973 | C | A | 2 | a0001c0001t0015g0137 a0001c0001t0015g0138 |
2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.25-5588C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218574973 | |||||||
| chr2:218575123 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.25-5438A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575123 | |||||||
| chr2:218575387 | C | CT | 36 | a0001c0001t0001g0120 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
55 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(52): Show |
intron_variant | MODIFIER | c.25-5157dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218575387 | ||||||
| chr2:218575424 | A | AGCTCAGG others(33): Show |
2 | a0001c0001t0002g0087 a0001c0001t0005g0053 |
2 | HG00323.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.25-5135_25-5096dup others(40): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218575424 | ||||||
| chr2:218575446 | C | T | 15 | a0001c0001t0003g0034 a0001c0001t0003g0157 a0001c0001t0003g0158 others(12): Show |
15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.25-5115C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575446 | |||||||
| chr2:218575513 | C | T | 8 | a0001c0001t0009g0033 a0001c0001t0009g0139 a0001c0001t0015g0033 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.25-5048C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575513 | |||||||
| chr2:218575568 | A | G | 2 | a0001c0001t0006g0016 a0001c0001t0006g0141 |
4 | HG02723.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-4993A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575568 | |||||||
| chr2:218575627 | A | G | 8 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0141 others(5): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.25-4934A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575627 | |||||||
| chr2:218575697 | C | T | 3 | a0001c0001t0004g0183 a0001c0001t0004g0185 a0001c0001t0048g0184 |
3 | NA19009.hp2 NA19056.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.25-4864C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575697 | |||||||
| chr2:218575705 | A | G | 30 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(27): Show |
46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-4856A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575705 | |||||||
| chr2:218575727 | G | A | 9 | a0001c0001t0003g0034 a0001c0001t0003g0157 a0001c0001t0003g0158 others(6): Show |
9 | HG02145.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-4834G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575727 | |||||||
| chr2:218575810 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(209): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.25-4751A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575810 | |||||||
| chr2:218575843 | G | A | 5 | a0001c0001t0022g0018 a0001c0001t0022g0161 a0001c0001t0027g0018 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-4718G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575843 | |||||||
| chr2:218575868 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0007g0109 |
2 | NA18977.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.25-4693T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575868 | |||||||
| chr2:218575920 | A | C | 11 | a0001c0001t0004g0010 a0001c0001t0004g0011 a0001c0001t0004g0035 others(8): Show |
19 | HG02135.hp2 HG02165.hp2 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.25-4641A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218575920 | |||||||
| chr2:218576184 | G | T | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.25-4377G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576184 | |||||||
| chr2:218576442 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.25-4119G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576442 | |||||||
| chr2:218576457 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.25-4104G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576457 | |||||||
| chr2:218576704 | A | G | 1 | a0001c0001t0050g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.25-3857A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576704 | |||||||
| chr2:218576705 | T | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(162): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.25-3856T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576705 | |||||||
| chr2:218576880 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(162): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.25-3681C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576880 | |||||||
| chr2:218576966 | C | CA | 149 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(146): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.25-3580dupA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218576966 | ||||||
| chr2:218576970 | A | AC | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.25-3591_25-3590ins others(1): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218576970 | |||||||
| chr2:218577694 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.25-2867A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577694 | |||||||
| chr2:218577702 | C | T | 32 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(29): Show |
51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.25-2859C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577702 | |||||||
| chr2:218577776 | A | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(32): Show |
74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.25-2785A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577776 | |||||||
| chr2:218577795 | A | C | 1 | a0001c0001t0009g0139 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.25-2766A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577795 | |||||||
| chr2:218577917 | G | A | 1 | a0001c0001t0038g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.25-2644G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218577917 | |||||||
| chr2:218578056 | G | C | 2 | a0001c0001t0007g0134 a0001c0001t0007g0135 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.25-2505G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578056 | |||||||
| chr2:218578278 | A | C | 165 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(162): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.25-2283A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578278 | |||||||
| chr2:218578359 | C | A | 2 | a0001c0001t0003g0164 a0001c0001t0005g0165 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.25-2202C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578359 | |||||||
| chr2:218578406 | A | G | 18 | a0001c0001t0009g0033 a0001c0001t0009g0139 a0001c0001t0014g0009 others(15): Show |
19 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.25-2155A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578406 | |||||||
| chr2:218578514 | A | G | 1 | a0001c0001t0007g0118 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.25-2047A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578514 | |||||||
| chr2:218578994 | A | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(31): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.25-1567A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218578994 | |||||||
| chr2:218579179 | A | G | 1 | a0001c0001t0010g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25-1382A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579179 | |||||||
| chr2:218579337 | A | G | 1 | a0001c0001t0049g0180 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.25-1224A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579337 | |||||||
| chr2:218579388 | T | C | 2 | a0001c0001t0043g0163 a0001c0001t0044g0154 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.25-1173T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579388 | |||||||
| chr2:218579392 | G | A | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.25-1169G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579392 | |||||||
| chr2:218579455 | A | T | 30 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(27): Show |
46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-1106A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579455 | |||||||
| chr2:218579509 | C | T | 1 | a0001c0001t0003g0079 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.25-1052C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579509 | |||||||
| chr2:218579520 | A | G | 1 | a0001c0001t0024g0128 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.25-1041A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579520 | |||||||
| chr2:218579609 | C | G | 32 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(29): Show |
51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.25-952C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579609 | |||||||
| chr2:218579631 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.25-930C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579631 | |||||||
| chr2:218579663 | T | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0097 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.25-898T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579663 | |||||||
| chr2:218579818 | A | G | 3 | a0001c0001t0014g0152 a0001c0001t0016g0078 a0001c0001t0042g0162 |
3 | HG00673.hp1 HG01109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.25-743A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579818 | |||||||
| chr2:218579871 | T | G | 30 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(27): Show |
46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.25-690T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579871 | |||||||
| chr2:218579922 | G | A | 1 | a0001c0001t0035g0057 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.25-639G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218579922 | |||||||
| chr2:218579982 | C | CT | 42 | a0001c0001t0001g0117 a0001c0001t0002g0013 a0001c0001t0002g0048 others(39): Show |
58 | HG00558.hp2 HG00621.hp1 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.25-562dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 218579982 | ||||||
| chr2:218580158 | G | A | 1 | a0001c0001t0042g0162 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.25-403G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218580158 | |||||||
| chr2:218580333 | A | G | 2 | a0001c0001t0007g0134 a0001c0001t0007g0135 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.25-228A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218580333 | |||||||
| chr2:218580402 | T | G | 1 | a0001c0001t0049g0180 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.25-159T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218580402 | |||||||
| chr2:218580442 | T | C | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.25-119T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 1/7 | chr2 | 218580442 | |||||||
| chr2:218581099 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.204+359G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581099 | |||||||
| chr2:218581129 | A | G | 5 | a0001c0001t0009g0033 a0001c0001t0015g0033 a0001c0001t0015g0137 others(2): Show |
5 | HG02257.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+389A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581129 | |||||||
| chr2:218581137 | GAA | G | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.204+399_204+400del others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218581137 | ||||||
| chr2:218581159 | T | G | 1 | a0001c0001t0002g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.204+419T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581159 | |||||||
| chr2:218581170 | C | CT | 8 | a0001c0001t0002g0080 a0001c0001t0006g0016 a0001c0001t0006g0017 others(5): Show |
12 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+446dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218581170 | ||||||
| chr2:218581170 | CT | C | 31 | a0001c0001t0003g0164 a0001c0001t0004g0006 a0001c0001t0004g0007 others(28): Show |
50 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(47): Show |
intron_variant | MODIFIER | c.204+446delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218581170 | ||||||
| chr2:218581171 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.204+431T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581171 | |||||||
| chr2:218581175 | T | C | 1 | a0001c0001t0004g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.204+435T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581175 | |||||||
| chr2:218581191 | C | T | 1 | a0001c0001t0006g0149 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.204+451C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581191 | |||||||
| chr2:218581192 | G | A | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+452G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581192 | |||||||
| chr2:218581402 | C | T | 1 | a0001c0001t0049g0180 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.204+662C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581402 | |||||||
| chr2:218581418 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.204+678C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581418 | |||||||
| chr2:218581734 | C | T | 4 | a0001c0001t0002g0013 a0001c0001t0002g0093 a0001c0001t0003g0013 others(1): Show |
4 | HG02083.hp2 NA18995.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+994C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581734 | |||||||
| chr2:218581754 | G | A | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.204+1014G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581754 | |||||||
| chr2:218581778 | A | G | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+1038A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581778 | |||||||
| chr2:218581987 | T | C | 8 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0141 others(5): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-984T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218581987 | |||||||
| chr2:218582090 | GA | G | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.205-873delA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218582090 | ||||||
| chr2:218582105 | T | C | 1 | a0001c0001t0045g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.205-866T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582105 | |||||||
| chr2:218582242 | C | T | 2 | a0001c0001t0005g0160 a0001c0001t0010g0179 |
2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.205-729C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582242 | |||||||
| chr2:218582400 | A | G | 8 | a0001c0001t0009g0033 a0001c0001t0009g0139 a0001c0001t0015g0033 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-571A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582400 | |||||||
| chr2:218582456 | C | T | 3 | a0001c0001t0003g0034 a0001c0001t0005g0034 a0001c0001t0009g0159 |
3 | HG02280.hp2 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.205-515C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582456 | |||||||
| chr2:218582487 | G | C | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-484G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582487 | |||||||
| chr2:218582488 | A | T | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-483A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582488 | |||||||
| chr2:218582490 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-481A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582490 | |||||||
| chr2:218582492 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-479C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582492 | |||||||
| chr2:218582494 | T | A | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-477T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582494 | |||||||
| chr2:218582496 | C | A | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-475C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582496 | |||||||
| chr2:218582498 | G | T | 1 | a0001c0001t0002g0058 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.205-473G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582498 | |||||||
| chr2:218582590 | T | G | 1 | a0001c0001t0050g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.205-381T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582590 | |||||||
| chr2:218582665 | G | A | 32 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(29): Show |
51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.205-306G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582665 | |||||||
| chr2:218582685 | G | A | 30 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(27): Show |
46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.205-286G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | chr2 | 218582685 | |||||||
| chr2:218582689 | C | CA | 33 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(30): Show |
52 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.205-271dupA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218582689 | ||||||
| chr2:218582889 | CT | C | 53 | a0001c0001t0001g0110 a0001c0001t0001g0121 a0001c0001t0003g0034 others(50): Show |
62 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.205-69delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 218582889 | ||||||
| chr2:218583189 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(211): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.320+103A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583189 | |||||||
| chr2:218583219 | G | C | 1 | a0001c0001t0004g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.320+133G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583219 | |||||||
| chr2:218583219 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0004g0181 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.320+135_320+158del others(24): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583219 | ||||||
| chr2:218583219 | GTGTGTGT others(27): Show |
G | 1 | a0001c0001t0010g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.320+135_320+168del others(34): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583219 | ||||||
| chr2:218583221 | GTGTGTGT others(13): Show |
G | 1 | a0001c0001t0004g0187 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.320+137_320+156del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583221 | ||||||
| chr2:218583221 | GTGTGTGT others(15): Show |
G | 6 | a0001c0001t0004g0011 a0001c0001t0004g0035 a0001c0001t0004g0167 others(3): Show |
7 | HG02074.hp2 HG03654.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+137_320+158del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583221 | ||||||
| chr2:218583221 | GTGTGTGT others(17): Show |
G | 13 | a0001c0001t0004g0006 a0001c0001t0004g0010 a0001c0001t0004g0035 others(10): Show |
18 | HG00558.hp2 HG00621.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.320+137_320+160del others(24): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583221 | ||||||
| chr2:218583221 | GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0004g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.320+137_320+164del others(28): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583221 | ||||||
| chr2:218583223 | GTGTGTGT others(11): Show |
G | 4 | a0001c0001t0004g0175 a0001c0001t0010g0007 a0001c0001t0010g0166 others(1): Show |
4 | NA18968.hp1 NA19012.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.320+139_320+156del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583223 | ||||||
| chr2:218583223 | GTGTGTGT others(13): Show |
G | 4 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0169 others(1): Show |
7 | HG02083.hp1 NA18939.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+139_320+158del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583223 | ||||||
| chr2:218583223 | GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0004g0011 | 2 | NA18612.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.320+139_320+160del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583223 | ||||||
| chr2:218583225 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0005g0160 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.320+141_320+152del others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | ||||||
| chr2:218583225 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0015 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.320+141_320+154del others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | ||||||
| chr2:218583225 | GTGTGTGT others(9): Show |
G | 2 | a0001c0001t0003g0034 a0001c0001t0009g0156 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.320+141_320+156del others(16): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | ||||||
| chr2:218583225 | GTGTGTGT others(11): Show |
G | 3 | a0001c0001t0003g0158 a0001c0001t0005g0034 a0001c0001t0009g0159 |
3 | HG02280.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.320+141_320+158del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | ||||||
| chr2:218583225 | GTGTGTGT others(13): Show |
G | 1 | a0001c0001t0003g0157 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.320+141_320+160del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | ||||||
| chr2:218583225 | GTGTGTGT others(21): Show |
G | 4 | a0001c0001t0002g0002 a0001c0001t0003g0085 a0001c0001t0005g0027 others(1): Show |
5 | HG00733.hp2 HG00735.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.320+141_320+168del others(28): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | ||||||
| chr2:218583225 | GTGTGTGT others(23): Show |
G | 1 | a0001c0001t0012g0008 | 4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.320+141_320+170del others(30): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583225 | ||||||
| chr2:218583227 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.320+143_320+156del others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | ||||||
| chr2:218583227 | GTGTGTGT others(9): Show |
G | 2 | a0001c0001t0001g0001 a0001c0001t0011g0001 |
2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.320+143_320+158del others(16): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | ||||||
| chr2:218583227 | GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0041g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.320+143_320+160del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | ||||||
| chr2:218583227 | GTGTGTGT others(13): Show |
G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0115 |
2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.320+143_320+162del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | ||||||
| chr2:218583227 | GTGTGTGT others(15): Show |
G | 6 | a0001c0001t0003g0164 a0001c0001t0005g0165 a0001c0001t0012g0136 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.320+143_320+164del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | ||||||
| chr2:218583227 | GTGTGTGT others(17): Show |
G | 1 | a0001c0001t0003g0002 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.320+143_320+166del others(24): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | ||||||
| chr2:218583227 | GTGTGTGT others(19): Show |
G | 5 | a0001c0001t0002g0002 a0001c0001t0002g0044 a0001c0001t0002g0049 others(2): Show |
5 | HG00639.hp2 HG02155.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+143_320+168del others(26): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | ||||||
| chr2:218583227 | GTGTGTGT others(21): Show |
G | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(60): Show |
85 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.320+143_320+170del others(28): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | ||||||
| chr2:218583227 | GTGTGTGT others(25): Show |
G | 1 | a0001c0001t0002g0071 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.320+143_320+174del others(32): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583227 | ||||||
| chr2:218583229 | GTGTGTCT others(3): Show |
G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0108 a0001c0001t0001g0110 others(2): Show |
7 | NA18950.hp2 NA18953.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.320+145_320+154del others(10): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | ||||||
| chr2:218583229 | GTGTGTCT others(5): Show |
G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(5): Show |
9 | HG00280.hp1 HG00639.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.320+145_320+156del others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | ||||||
| chr2:218583229 | GTGTGTCT others(7): Show |
G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0117 others(3): Show |
16 | HG00558.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.320+145_320+158del others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | ||||||
| chr2:218583229 | GTGTGTCT others(9): Show |
G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0122 others(3): Show |
12 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.320+145_320+160del others(16): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | ||||||
| chr2:218583229 | GTGTGTCT others(11): Show |
G | 2 | a0001c0001t0001g0014 a0001c0001t0042g0162 |
2 | HG01109.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.320+145_320+162del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | ||||||
| chr2:218583229 | GTGTGTCT others(13): Show |
G | 2 | a0001c0001t0050g0119 a0001c0001t0056g0107 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.320+145_320+164del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | ||||||
| chr2:218583229 | GTGTGTCT others(15): Show |
G | 1 | a0001c0001t0001g0001 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.320+145_320+166del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | ||||||
| chr2:218583229 | GTGTGTCT others(19): Show |
G | 40 | a0001c0001t0002g0002 a0001c0001t0002g0046 a0001c0001t0002g0056 others(37): Show |
46 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.320+145_320+170del others(26): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | ||||||
| chr2:218583229 | GTGTGTCT others(21): Show |
G | 1 | a0001c0001t0009g0139 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.320+145_320+172del others(28): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583229 | ||||||
| chr2:218583231 | GTGTCTCT others(3): Show |
G | 1 | a0001c0001t0007g0135 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.320+147_320+156del others(10): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | ||||||
| chr2:218583231 | GTGTCTCT others(5): Show |
G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0112 |
2 | NA19076.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.320+147_320+158del others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | ||||||
| chr2:218583231 | GTGTCTCT others(11): Show |
G | 2 | a0001c0001t0001g0014 a0001c0001t0022g0161 |
2 | HG03453.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.320+147_320+164del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | ||||||
| chr2:218583231 | GTGTCTCT others(17): Show |
G | 4 | a0001c0001t0002g0004 a0001c0001t0003g0004 a0001c0001t0003g0021 others(1): Show |
5 | HG02155.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+147_320+170del others(24): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | ||||||
| chr2:218583231 | GTGTCTCT others(27): Show |
G | 8 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0141 others(5): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.320+147_320+180del others(34): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583231 | ||||||
| chr2:218583233 | GTC | G | 2 | a0001c0001t0001g0005 a0001c0001t0052g0030 |
3 | HG02145.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.320+200_320+201del others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | ||||||
| chr2:218583233 | GTCTC | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0123 a0001c0001t0017g0005 |
6 | HG02109.hp2 HG02486.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.320+198_320+201del others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | ||||||
| chr2:218583233 | GTCTCTCT others(1): Show |
G | 3 | a0001c0001t0001g0116 a0001c0001t0013g0130 a0001c0001t0053g0133 |
3 | HG02572.hp2 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.320+194_320+201del others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | ||||||
| chr2:218583233 | GTCTCTCT others(3): Show |
G | 3 | a0001c0001t0004g0007 a0001c0001t0013g0131 a0001c0001t0024g0103 |
5 | HG01975.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+192_320+201del others(10): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | ||||||
| chr2:218583233 | GTCTCTCT others(5): Show |
G | 4 | a0001c0001t0013g0032 a0001c0001t0013g0129 a0001c0001t0023g0031 others(1): Show |
6 | HG02886.hp1 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.320+190_320+201del others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | ||||||
| chr2:218583233 | GTCTCTCT others(7): Show |
G | 3 | a0001c0001t0018g0126 a0001c0001t0024g0128 a0001c0001t0055g0104 |
3 | HG02896.hp2 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.320+188_320+201del others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | ||||||
| chr2:218583233 | GTCTCTCT others(11): Show |
G | 1 | a0001c0001t0018g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.320+184_320+201del others(18): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | ||||||
| chr2:218583233 | GTCTCTCT others(13): Show |
G | 1 | a0001c0001t0001g0014 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.320+182_320+201del others(20): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | ||||||
| chr2:218583233 | GTCTCTCT others(15): Show |
G | 2 | a0001c0001t0002g0075 a0001c0001t0016g0140 |
2 | HG03516.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.320+180_320+201del others(22): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583233 | ||||||
| chr2:218583235 | C | G | 1 | a0001c0001t0018g0127 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.320+149C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583235 | |||||||
| chr2:218583237 | C | G | 3 | a0001c0001t0001g0005 a0001c0001t0018g0127 a0001c0001t0052g0030 |
4 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.320+151C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583237 | |||||||
| chr2:218583239 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0123 a0001c0001t0017g0005 others(2): Show |
10 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.320+153C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583239 | |||||||
| chr2:218583241 | C | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0123 a0001c0001t0011g0188 others(4): Show |
12 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.320+155C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583241 | |||||||
| chr2:218583243 | C | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0123 others(7): Show |
15 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.320+157C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583243 | |||||||
| chr2:218583245 | C | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0123 others(7): Show |
15 | HG01975.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.320+159C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583245 | |||||||
| chr2:218583247 | C | G | 10 | a0001c0001t0001g0116 a0001c0001t0011g0188 a0001c0001t0013g0032 others(7): Show |
12 | HG01975.hp1 HG02451.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.320+161C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583247 | |||||||
| chr2:218583249 | C | G | 11 | a0001c0001t0001g0116 a0001c0001t0011g0188 a0001c0001t0013g0032 others(8): Show |
13 | HG01975.hp1 HG02451.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.320+163C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583249 | |||||||
| chr2:218583251 | C | G | 8 | a0001c0001t0011g0188 a0001c0001t0013g0131 a0001c0001t0018g0126 others(5): Show |
9 | HG01975.hp1 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.320+165C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583251 | |||||||
| chr2:218583253 | C | G | 5 | a0001c0001t0018g0125 a0001c0001t0018g0126 a0001c0001t0024g0103 others(2): Show |
5 | HG01975.hp1 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.320+167C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583253 | |||||||
| chr2:218583255 | C | G | 3 | a0001c0001t0018g0125 a0001c0001t0018g0126 a0001c0001t0024g0128 |
3 | HG02723.hp1 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.320+169C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583255 | |||||||
| chr2:218583257 | C | G | 4 | a0001c0001t0002g0075 a0001c0001t0018g0125 a0001c0001t0018g0126 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.320+171C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583257 | |||||||
| chr2:218583265 | C | T | 1 | a0001c0001t0013g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.320+179C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583265 | |||||||
| chr2:218583286 | TC | T | 3 | a0001c0001t0001g0117 a0001c0001t0004g0176 a0001c0001t0010g0177 |
3 | HG01175.hp1 NA19012.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.320+202delC | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 218583286 | ||||||
| chr2:218583842 | G | A | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.320+756G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218583842 | |||||||
| chr2:218584139 | G | T | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.321-473G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218584139 | |||||||
| chr2:218584294 | G | A | 3 | a0001c0001t0004g0170 a0001c0001t0004g0176 a0001c0001t0010g0171 |
3 | HG02074.hp2 NA18981.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.321-318G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218584294 | |||||||
| chr2:218584320 | G | T | 9 | a0001c0001t0003g0034 a0001c0001t0003g0157 a0001c0001t0003g0158 others(6): Show |
9 | HG02145.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.321-292G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218584320 | |||||||
| chr2:218584370 | C | G | 2 | a0001c0001t0007g0134 a0001c0001t0007g0135 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.321-242C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 3/7 | chr2 | 218584370 | |||||||
| chr2:218584761 | C | A | 8 | a0001c0001t0009g0033 a0001c0001t0009g0139 a0001c0001t0015g0033 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+40C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218584761 | |||||||
| chr2:218585020 | G | A | 1 | a0001c0001t0018g0127 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.430+299G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585020 | |||||||
| chr2:218585059 | C | T | 1 | a0001c0001t0003g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.430+338C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585059 | |||||||
| chr2:218585166 | C | G | 1 | a0001c0001t0009g0139 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.430+445C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585166 | |||||||
| chr2:218585236 | GTCTTACT | G | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.430+519_430+525del others(7): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218585236 | ||||||
| chr2:218585366 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(209): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.430+645C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585366 | |||||||
| chr2:218585574 | C | CA | 162 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(159): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.430+865dupA | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218585574 | ||||||
| chr2:218585641 | T | TTA | 179 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0123 others(176): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.430+921_430+922ins others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218585641 | ||||||
| chr2:218585642 | T | TTTA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(25): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.430+923_430+924ins others(3): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218585642 | ||||||
| chr2:218585643 | T | A | 2 | a0001c0001t0007g0134 a0001c0001t0007g0135 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.430+922T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585643 | |||||||
| chr2:218585645 | T | A | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+924T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585645 | |||||||
| chr2:218585646 | T | A | 130 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(127): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.430+925T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585646 | |||||||
| chr2:218585647 | T | A | 1 | a0001c0001t0002g0073 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.430+926T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585647 | |||||||
| chr2:218585651 | T | A | 2 | a0001c0001t0003g0081 a0001c0001t0004g0170 |
2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.430+930T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585651 | |||||||
| chr2:218585663 | A | G | 1 | a0001c0001t0006g0147 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.430+942A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585663 | |||||||
| chr2:218585824 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.430+1103G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585824 | |||||||
| chr2:218585873 | C | T | 30 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(27): Show |
46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.430+1152C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585873 | |||||||
| chr2:218585892 | T | G | 2 | a0001c0001t0043g0163 a0001c0001t0044g0154 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.430+1171T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218585892 | |||||||
| chr2:218586164 | A | G | 5 | a0001c0001t0018g0125 a0001c0001t0018g0126 a0001c0001t0018g0127 others(2): Show |
6 | HG02723.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-1422A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586164 | |||||||
| chr2:218586292 | T | G | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.431-1294T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586292 | |||||||
| chr2:218586313 | A | G | 2 | a0001c0001t0019g0143 a0001c0001t0019g0144 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.431-1273A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586313 | |||||||
| chr2:218586339 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.431-1247G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586339 | |||||||
| chr2:218586488 | C | CT | 23 | a0001c0001t0001g0029 a0001c0001t0002g0087 a0001c0001t0003g0021 others(20): Show |
24 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.431-1082dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218586488 | ||||||
| chr2:218586650 | G | A | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-936G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586650 | |||||||
| chr2:218586687 | C | T | 7 | a0001c0001t0002g0003 a0001c0001t0002g0024 a0001c0001t0002g0072 others(4): Show |
14 | HG01070.hp1 HG02071.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.431-899C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218586687 | |||||||
| chr2:218587051 | T | C | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.431-535T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218587051 | |||||||
| chr2:218587191 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(209): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.431-395A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218587191 | |||||||
| chr2:218587311 | C | T | 1 | a0001c0001t0018g0127 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.431-275C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | chr2 | 218587311 | |||||||
| chr2:218587427 | CT | C | 18 | a0001c0001t0003g0034 a0001c0001t0003g0042 a0001c0001t0003g0062 others(15): Show |
18 | HG01109.hp1 HG01884.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.431-148delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 218587427 | ||||||
| chr2:218587774 | T | C | 6 | a0001c0001t0009g0033 a0001c0001t0009g0139 a0001c0001t0015g0033 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+79T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218587774 | |||||||
| chr2:218588053 | C | A | 1 | a0001c0001t0054g0105 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.540+358C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588053 | |||||||
| chr2:218588202 | T | G | 1 | a0001c0001t0001g0014 | 3 | NA19055.hp2 NA19074.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.540+507T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588202 | |||||||
| chr2:218588287 | C | CTTTTTT | 29 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(26): Show |
45 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(42): Show |
intron_variant | MODIFIER | c.540+602_540+607dup others(6): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588287 | ||||||
| chr2:218588374 | C | T | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.540+679C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588374 | |||||||
| chr2:218588407 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.540+712G>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588407 | |||||||
| chr2:218588415 | A | G | 15 | a0001c0001t0003g0034 a0001c0001t0003g0157 a0001c0001t0003g0158 others(12): Show |
15 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.540+720A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588415 | |||||||
| chr2:218588434 | A | G | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.540+739A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588434 | |||||||
| chr2:218588512 | C | A | 9 | a0001c0001t0013g0032 a0001c0001t0013g0129 a0001c0001t0013g0130 others(6): Show |
11 | HG02723.hp1 HG02886.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.540+817C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588512 | |||||||
| chr2:218588513 | C | T | 165 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(162): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.540+818C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588513 | |||||||
| chr2:218588588 | C | CT | 10 | a0001c0001t0007g0135 a0001c0001t0009g0033 a0001c0001t0014g0142 others(7): Show |
10 | HG02257.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+919dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | C | CTTT | 8 | a0001c0001t0002g0089 a0001c0001t0003g0038 a0001c0001t0005g0064 others(5): Show |
11 | HG00099.hp2 HG02717.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.540+917_540+919dup others(3): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | C | CTTTT | 59 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0013 others(56): Show |
91 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.540+916_540+919dup others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | C | CTTTTT | 33 | a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0070 others(30): Show |
44 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.540+915_540+919dup others(5): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | C | CTTTTTT | 7 | a0001c0001t0002g0024 a0001c0001t0006g0141 a0001c0001t0006g0146 others(4): Show |
8 | HG02257.hp2 HG02451.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.540+914_540+919dup others(6): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0004g0169 a0001c0001t0013g0129 |
2 | HG02083.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.540+909_540+919dup others(11): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0004g0172 a0001c0001t0004g0173 a0001c0001t0018g0126 others(1): Show |
4 | HG00558.hp2 HG02896.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+908_540+919dup others(12): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | C | CTTTTTTT others(6): Show |
17 | a0001c0001t0004g0006 a0001c0001t0004g0010 a0001c0001t0004g0167 others(14): Show |
25 | HG00621.hp1 HG02165.hp2 HG02723.hp1 others(22): Show |
intron_variant | MODIFIER | c.540+907_540+919dup others(13): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | C | CTTTTTTT others(7): Show |
12 | a0001c0001t0004g0007 a0001c0001t0004g0011 a0001c0001t0004g0035 others(9): Show |
20 | HG02027.hp2 HG02074.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.540+906_540+919dup others(14): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0004g0036 a0001c0001t0004g0181 a0001c0001t0004g0185 |
4 | HG02135.hp2 NA18952.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.540+905_540+919dup others(15): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | CTT | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(28): Show |
69 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.540+918_540+919del others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588588 | CTTTT | C | 14 | a0001c0001t0003g0034 a0001c0001t0003g0157 a0001c0001t0003g0158 others(11): Show |
14 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+916_540+919del others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588588 | ||||||
| chr2:218588604 | T | G | 1 | a0001c0001t0041g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.540+909T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588604 | |||||||
| chr2:218588633 | C | T | 32 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(29): Show |
51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.540+938C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218588633 | |||||||
| chr2:218588733 | A | AT | 86 | a0001c0001t0001g0114 a0001c0001t0002g0002 a0001c0001t0002g0003 others(83): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.540+1051dupT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588733 | ||||||
| chr2:218588733 | A | ATT | 5 | a0001c0001t0002g0025 a0001c0001t0002g0094 a0001c0001t0003g0027 others(2): Show |
6 | HG02698.hp2 NA18950.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+1050_540+1051d others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218588733 | ||||||
| chr2:218589156 | T | C | 32 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(29): Show |
51 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(48): Show |
intron_variant | MODIFIER | c.540+1461T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589156 | |||||||
| chr2:218589387 | C | T | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+1692C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589387 | |||||||
| chr2:218589565 | G | A | 1 | a0001c0001t0011g0188 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.540+1870G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589565 | |||||||
| chr2:218589688 | G | GTAGCCAC others(10): Show |
1 | a0001c0001t0031g0074 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.540+1994_540+1995i others(19): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218589688 | ||||||
| chr2:218589763 | C | G | 1 | a0001c0001t0002g0022 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.540+2068C>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589763 | |||||||
| chr2:218589806 | T | C | 30 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(27): Show |
46 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(43): Show |
intron_variant | MODIFIER | c.540+2111T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589806 | |||||||
| chr2:218589946 | A | G | 1 | a0001c0001t0026g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.540+2251A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589946 | |||||||
| chr2:218589947 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.540+2252C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218589947 | |||||||
| chr2:218590051 | T | A | 1 | a0001c0001t0005g0160 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.541-2253T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590051 | |||||||
| chr2:218590054 | GT | G | 130 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(127): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.541-2239delT | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590054 | ||||||
| chr2:218590060 | T | G | 6 | a0001c0001t0009g0033 a0001c0001t0009g0139 a0001c0001t0015g0033 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-2244T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590060 | |||||||
| chr2:218590063 | T | G | 15 | a0001c0001t0001g0114 a0001c0001t0002g0022 a0001c0001t0002g0066 others(12): Show |
16 | HG01258.hp1 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.541-2241T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590063 | |||||||
| chr2:218590063 | T | TTG | 31 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(28): Show |
50 | HG00558.hp2 HG00621.hp1 HG02027.hp2 others(47): Show |
intron_variant | MODIFIER | c.541-2240_541-2239i others(4): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590063 | ||||||
| chr2:218590078 | T | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(162): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.541-2226T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590078 | |||||||
| chr2:218590234 | A | T | 1 | a0001c0001t0009g0065 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541-2070A>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590234 | |||||||
| chr2:218590448 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(209): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.541-1856G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590448 | |||||||
| chr2:218590664 | T | C | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-1640T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590664 | |||||||
| chr2:218590797 | C | CTTG | 5 | a0001c0001t0004g0173 a0001c0001t0012g0008 a0001c0001t0012g0136 others(2): Show |
8 | HG00558.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-1483_541-1481d others(5): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590797 | ||||||
| chr2:218590797 | C | CTTGTTG | 29 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0010 others(26): Show |
45 | HG00621.hp1 HG02027.hp2 HG02074.hp2 others(42): Show |
intron_variant | MODIFIER | c.541-1486_541-1481d others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590797 | ||||||
| chr2:218590797 | CTTG | C | 107 | a0001c0001t0001g0122 a0001c0001t0002g0002 a0001c0001t0002g0003 others(104): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.541-1483_541-1481d others(5): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590797 | ||||||
| chr2:218590797 | CTTGTTG | C | 8 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0141 others(5): Show |
12 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.541-1486_541-1481d others(8): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 218590797 | ||||||
| chr2:218590811 | T | C | 1 | a0001c0001t0022g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.541-1493T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590811 | |||||||
| chr2:218590865 | G | A | 1 | a0001c0001t0004g0174 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.541-1439G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218590865 | |||||||
| chr2:218591052 | G | A | 10 | a0001c0001t0014g0009 a0001c0001t0014g0142 a0001c0001t0014g0152 others(7): Show |
11 | HG02486.hp2 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-1252G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591052 | |||||||
| chr2:218591166 | A | G | 1 | a0001c0001t0002g0071 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.541-1138A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591166 | |||||||
| chr2:218591244 | G | T | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.541-1060G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591244 | |||||||
| chr2:218591252 | A | G | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-1052A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591252 | |||||||
| chr2:218591549 | C | A | 1 | a0001c0001t0007g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.541-755C>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591549 | |||||||
| chr2:218591613 | G | A | 2 | a0001c0001t0002g0056 a0001c0001t0002g0097 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.541-691G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591613 | |||||||
| chr2:218591618 | C | T | 1 | a0001c0001t0048g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.541-686C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591618 | |||||||
| chr2:218591694 | A | G | 165 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(162): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.541-610A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218591694 | |||||||
| chr2:218592006 | C | T | 6 | a0001c0001t0009g0033 a0001c0001t0009g0139 a0001c0001t0015g0033 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-298C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592006 | |||||||
| chr2:218592014 | A | G | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.541-290A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592014 | |||||||
| chr2:218592047 | C | T | 1 | a0001c0001t0048g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.541-257C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592047 | |||||||
| chr2:218592082 | C | T | 2 | a0001c0001t0002g0068 a0001c0001t0002g0070 |
2 | HG00438.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.541-222C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592082 | |||||||
| chr2:218592122 | G | A | 3 | a0001c0001t0014g0142 a0001c0001t0019g0143 a0001c0001t0019g0144 |
3 | HG02630.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.541-182G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592122 | |||||||
| chr2:218592141 | A | G | 2 | a0001c0001t0012g0008 a0001c0001t0012g0136 |
5 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-163A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592141 | |||||||
| chr2:218592186 | A | C | 1 | a0001c0001t0003g0067 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.541-118A>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592186 | |||||||
| chr2:218592226 | T | G | 1 | a0001c0001t0003g0085 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.541-78T>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 5/7 | chr2 | 218592226 | |||||||
| chr2:218592471 | A | G | 1 | a0001c0001t0005g0026 | 2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.639+69A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 6/7 | chr2 | 218592471 | |||||||
| chr2:218592535 | A | G | 1 | a0001c0001t0003g0021 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.640-81A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 6/7 | chr2 | 218592535 | |||||||
| chr2:218592946 | G | A | 1 | a0001c0001t0035g0057 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.731+239G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218592946 | |||||||
| chr2:218593008 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(31): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.731+301C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593008 | |||||||
| chr2:218593018 | G | A | 165 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(162): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.731+311G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593018 | |||||||
| chr2:218593152 | TTC | T | 5 | a0001c0001t0022g0018 a0001c0001t0022g0161 a0001c0001t0027g0018 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.731+447_731+448del others(2): Show |
CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 218593152 | ||||||
| chr2:218593472 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.732-636A>G | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593472 | |||||||
| chr2:218593631 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0003g0019 |
2 | HG01255.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.732-477C>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593631 | |||||||
| chr2:218593775 | T | A | 4 | a0001c0001t0018g0125 a0001c0001t0018g0126 a0001c0001t0018g0127 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.732-333T>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593775 | |||||||
| chr2:218593899 | G | A | 1 | a0001c0001t0008g0060 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.732-209G>A | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593899 | |||||||
| chr2:218593933 | T | C | 133 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(130): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.732-175T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593933 | |||||||
| chr2:218593981 | G | T | 2 | a0001c0001t0003g0164 a0001c0001t0005g0165 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.732-127G>T | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218593981 | |||||||
| chr2:218594084 | T | C | 2 | a0001c0001t0003g0164 a0001c0001t0005g0165 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.732-24T>C | CNOT9 | ENSG00000144580.15 | transcript | ENST00000273064.11 | protein_coding | 7/7 | chr2 | 218594084 |