Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10669 |
| ensemblid | ENSG00000138028.17 |
| hgncid | 16962 |
| symbol | CGREF1 |
| name | cell growth regulator with EF-hand domain 1 |
| refseq_nuc | NM_006569.6 |
| refseq_prot | NP_006560.3 |
| ensembl_nuc | ENST00000402394.6 |
| ensembl_prot | ENSP00000385452.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 27100594 |
| end | 27119128 |
| strand | - |
| ver | v1.2 |
| region | chr2:27100594-27119128 |
| region5000 | chr2:27095594-27124128 |
| regionname0 | CGREF1_chr2_27100594_27119128 |
| regionname5000 | CGREF1_chr2_27095594_27124128 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 301 | 329 | 80 | 76 | 119 | 18 | 35 | 87 | CGREF1_chr2_27095594_27124128 | CGREF1 | MLPLT others(296): Show |
chr2 | 27095594 | 27124128 |
| a0002 | 1/0 | 318 | 14 | 12 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | MLPLT others(313): Show |
chr2 | 27095594 | 27124128 |
| a0003 | 0/0 | 301 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | CGREF1_chr2_27095594_27124128 | CGREF1 | MLPLT others(296): Show |
chr2 | 27095594 | 27124128 |
| a0004 | 0/0 | 301 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | MLPLT others(296): Show |
chr2 | 27095594 | 27124128 |
| a0005 | 0/0 | 301 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | MLPLT others(296): Show |
chr2 | 27095594 | 27124128 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 903 | 167 | 22 | 36 | 73 | 11 | 24 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 | ||
| a0001c0002 | 0/0 | 903 | 146 | 50 | 39 | 40 | 7 | 10 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 | ||
| a0001c0004 | 0/0 | 903 | 12 | 7 | 1 | 4 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 | ||
| a0001c0008 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 | ||
| a0001c0009 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 | ||
| a0001c0011 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 | ||
| a0001c0012 | 0/0 | 903 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 | ||
| a0002c0003 | 1/0 | 954 | 12 | 10 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(949): Show |
chr2 | 27095594 | 27124128 | ||
| a0002c0007 | 0/0 | 954 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(949): Show |
chr2 | 27095594 | 27124128 | ||
| a0003c0005 | 0/0 | 903 | 6 | 0 | 0 | 6 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 | ||
| a0004c0006 | 0/0 | 903 | 2 | 0 | 1 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 | ||
| a0005c0010 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ATGTT others(898): Show |
chr2 | 27095594 | 27124128 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1881 | 158 | 22 | 32 | 70 | 10 | 23 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0001t0002 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0001c0001t0006 | 0/0 | 1881 | 3 | 0 | 1 | 0 | 1 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0001t0010 | 0/0 | 1881 | 2 | 0 | 2 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0001t0011 | 0/0 | 1881 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0001t0012 | 0/0 | 1881 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0001t0014 | 0/0 | 1881 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0002t0001 | 0/0 | 1881 | 19 | 14 | 5 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0002t0002 | 0/0 | 1880 | 110 | 24 | 30 | 40 | 7 | 9 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0001c0002t0004 | 0/0 | 1880 | 5 | 4 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0001c0002t0005 | 0/0 | 1880 | 5 | 3 | 2 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0001c0002t0007 | 0/0 | 1881 | 3 | 3 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0002t0008 | 0/0 | 1881 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0002t0013 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0001c0002t0017 | 0/0 | 1880 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0001c0004t0001 | 0/0 | 1881 | 10 | 6 | 1 | 3 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0004t0015 | 0/0 | 1881 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0004t0016 | 0/0 | 1881 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0008t0001 | 0/0 | 1881 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0001c0009t0002 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0001c0011t0002 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0001c0012t0002 | 0/0 | 1880 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0002c0003t0002 | 0/0 | 1931 | 2 | 1 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1926): Show |
chr2 | 27095594 | 27124128 |
| a0002c0003t0003 | 1/0 | 1931 | 7 | 6 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1926): Show |
chr2 | 27095594 | 27124128 |
| a0002c0003t0009 | 0/0 | 1931 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1926): Show |
chr2 | 27095594 | 27124128 |
| a0002c0003t0018 | 0/0 | 1931 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1926): Show |
chr2 | 27095594 | 27124128 |
| a0002c0007t0002 | 0/0 | 1931 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1926): Show |
chr2 | 27095594 | 27124128 |
| a0003c0005t0001 | 0/0 | 1881 | 6 | 0 | 0 | 6 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1876): Show |
chr2 | 27095594 | 27124128 |
| a0004c0006t0002 | 0/0 | 1880 | 2 | 0 | 1 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| a0005c0010t0002 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | ACACA others(1875): Show |
chr2 | 27095594 | 27124128 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0010g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0011g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0001t0014g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0001 | 0/0 | 14 | 0 | 4 | 10 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0002 | 0/0 | 7 | 3 | 2 | 0 | 1 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0004 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0004g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0005g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0005g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0007g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0008g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0013g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0002t0017g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0004t0016g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0009t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0011t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0001c0012t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0003g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0003t0018g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0007t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0002c0007t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0003c0005t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0003c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0003c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0003c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0003c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0003c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0004c0006t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0004c0006t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| a0005c0010t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | GBR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0045 | EUR | GBR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | GBR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0052 | EUR | FIN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | FIN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0042 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00673 | hp2 | a0001 | c0001 | t0011 | g0030 | EAS | CHS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00733 | hp2 | a0001 | c0002 | t0005 | g0014 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00738 | hp1 | a0001 | c0002 | t0004 | g0021 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00738 | hp2 | a0004 | c0006 | t0002 | g0098 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0070 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0049 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01109 | hp2 | a0002 | c0003 | t0002 | g0120 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01167 | hp1 | a0001 | c0002 | t0005 | g0014 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0210 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0284 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0050 | AMR | PUR | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01256 | hp2 | a0001 | c0001 | t0010 | g0205 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01257 | hp2 | a0001 | c0001 | t0010 | g0168 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01346 | hp2 | a0001 | c0001 | t0014 | g0197 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01358 | hp2 | a0001 | c0002 | t0013 | g0092 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0011 | EUR | IBS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | IBS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0273 | EUR | IBS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0011 | EUR | IBS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01884 | hp1 | a0001 | c0011 | t0002 | g0117 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0029 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0121 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0069 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0104 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02015 | hp2 | a0001 | c0009 | t0002 | g0084 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0097 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CDX | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CDX | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02257 | hp1 | a0001 | c0004 | t0016 | g0292 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0078 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0073 | AMR | PEL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02451 | hp1 | a0001 | c0002 | t0005 | g0013 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02615 | hp2 | a0002 | c0003 | t0009 | g0088 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0076 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02738 | hp1 | a0001 | c0002 | t0017 | g0294 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02895 | hp1 | a0002 | c0003 | t0003 | g0025 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0094 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02897 | hp2 | a0002 | c0003 | t0003 | g0236 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0118 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0029 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02965 | hp2 | a0002 | c0003 | t0003 | g0025 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0119 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02976 | hp2 | a0002 | c0003 | t0018 | g0295 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03041 | hp1 | a0002 | c0003 | t0003 | g0170 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0293 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03130 | hp1 | a0001 | c0002 | t0007 | g0010 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0075 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03195 | hp1 | a0001 | c0002 | t0008 | g0015 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0040 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0013 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0116 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0063 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | ESN | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03540 | hp2 | a0002 | c0007 | t0002 | g0095 | AFR | GWD | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0190 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03669 | hp1 | a0001 | c0012 | t0002 | g0086 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | BEB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0044 | SAS | BEB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0254 | SAS | BEB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0099 | SAS | STU | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | STU | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18522 | hp1 | a0002 | c0003 | t0003 | g0208 | AFR | YRI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | YRI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18906 | hp1 | a0001 | c0002 | t0005 | g0043 | AFR | YRI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18906 | hp2 | a0001 | c0002 | t0007 | g0010 | AFR | YRI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18949 | hp1 | a0001 | c0008 | t0001 | g0182 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18960 | hp1 | a0003 | c0005 | t0001 | g0163 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18967 | hp2 | a0005 | c0010 | t0002 | g0074 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18968 | hp1 | a0001 | c0004 | t0001 | g0226 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18978 | hp1 | a0003 | c0005 | t0001 | g0135 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18980 | hp1 | a0003 | c0005 | t0001 | g0166 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18982 | hp2 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18985 | hp1 | a0001 | c0004 | t0001 | g0221 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19001 | hp2 | a0003 | c0005 | t0001 | g0139 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0068 | AFR | LWK | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | LWK | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | LWK | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0087 | AFR | LWK | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19065 | hp1 | a0001 | c0001 | t0012 | g0031 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19085 | hp2 | a0003 | c0005 | t0001 | g0192 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19086 | hp1 | a0003 | c0005 | t0001 | g0173 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA19240 | hp2 | a0001 | c0002 | t0008 | g0015 | AFR | YRI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | ASW | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20129 | hp2 | a0002 | c0003 | t0003 | g0195 | AFR | ASW | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0056 | EUR | TSI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20905 | hp1 | a0004 | c0006 | t0002 | g0066 | SAS | GIH | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | GIH | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0072 | AFR | ACB | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0021 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | MSL | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | USA | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| HG06807 | hp2 | a0001 | c0002 | t0007 | g0039 | AFR | USA | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA18955 | hp2 | a0001 | c0004 | t0015 | g0261 | EAS | JPT | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20300 | hp1 | a0002 | c0007 | t0002 | g0079 | AFR | USA | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA20300 | hp2 | a0002 | c0003 | t0009 | g0082 | AFR | USA | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | LWK | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0083 | AFR | LWK | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0200 | REF | REF | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0003 | g0179 | REF | REF | CGREF1_chr2_27095594_27124128 | CGREF1 | chr2 | 27095594 | 27124128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27101372 | C | T | 1 | a0001 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.859G>A | p.Glu287Lys | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 1153/1931 | 859/957 | 287/318 | chr2 | 27101372 | |||
| chr2:27101385 | GGCCTCTG others(44): Show |
G | 4 | a0001 a0003 a0004 others(1): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
disruptive_inframe_deletion | MODERATE | c.795_845delTGAAGGAG others(43): Show |
p.Glu266_Ala282del | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 1139/1931 | 795/957 | 265/318 | chr2 | 27101385 | |||
| chr2:27101710 | T | C | 1 | a0003 | 6 | NA18960.hp1 NA18978.hp1 NA18980.hp1 others(3): Show |
missense_variant | MODERATE | c.521A>G | p.Lys174Arg | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 815/1931 | 521/957 | 174/318 | chr2 | 27101710 | |||
| chr2:27101768 | G | C | 1 | a0005 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.463C>G | p.Pro155Ala | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 757/1931 | 463/957 | 155/318 | chr2 | 27101768 | |||
| chr2:27101801 | C | T | 1 | a0004 | 2 | HG00738.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.430G>A | p.Gly144Arg | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 724/1931 | 430/957 | 144/318 | chr2 | 27101801 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27101523 | A | G | 1 | a0002c0007 | 2 | HG03540.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.708T>C | p.Pro236Pro | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 1002/1931 | 708/957 | 236/318 | chr2 | 27101523 | |||
| chr2:27101856 | G | C | 4 | a0001c0001 a0001c0004 a0001c0008 others(1): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
synonymous_variant | LOW | c.375C>G | p.Thr125Thr | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 669/1931 | 375/957 | 125/318 | chr2 | 27101856 | |||
| chr2:27101862 | G | A | 1 | a0001c0011 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.369C>T | p.Leu123Leu | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 663/1931 | 369/957 | 123/318 | chr2 | 27101862 | |||
| chr2:27101874 | C | T | 1 | a0001c0009 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.357G>A | p.Val119Val | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 651/1931 | 357/957 | 119/318 | chr2 | 27101874 | |||
| chr2:27101883 | G | T | 3 | a0001c0001 a0001c0008 a0003c0005 |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
synonymous_variant | LOW | c.348C>A | p.Ile116Ile | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 642/1931 | 348/957 | 116/318 | chr2 | 27101883 | |||
| chr2:27102193 | G | A | 1 | a0001c0012 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.246C>T | p.Asp82Asp | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 5/6 | 540/1931 | 246/957 | 82/318 | chr2 | 27102193 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27100600 | A | C | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(26): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*674T>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 674 | chr2 | 27100600 | ||||||
| chr2:27100690 | A | G | 1 | a0001c0002t0013 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*584T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 584 | chr2 | 27100690 | ||||||
| chr2:27100750 | T | A | 1 | a0001c0001t0014 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*524A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 524 | chr2 | 27100750 | ||||||
| chr2:27100758 | G | A | 2 | a0001c0002t0004 a0001c0004t0015 |
6 | HG00738.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*516C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 516 | chr2 | 27100758 | ||||||
| chr2:27100759 | T | G | 1 | a0001c0002t0007 | 3 | HG03130.hp1 HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*515A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 515 | chr2 | 27100759 | ||||||
| chr2:27100784 | G | A | 1 | a0001c0004t0016 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 490 | chr2 | 27100784 | ||||||
| chr2:27100871 | G | A | 1 | a0001c0002t0005 | 5 | HG00733.hp2 HG01167.hp1 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*403C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 403 | chr2 | 27100871 | ||||||
| chr2:27100893 | A | G | 1 | a0002c0003t0009 | 2 | HG02615.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*381T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 381 | chr2 | 27100893 | ||||||
| chr2:27101068 | G | GC | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(11): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*205dupG | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 205 | chr2 | 27101068 | ||||||
| chr2:27101095 | T | G | 1 | a0001c0001t0010 | 2 | HG01256.hp2 HG01257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*179A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 179 | chr2 | 27101095 | ||||||
| chr2:27101125 | C | T | 1 | a0001c0002t0004 | 5 | HG00738.hp1 HG02922.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*149G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 149 | chr2 | 27101125 | ||||||
| chr2:27101168 | G | A | 13 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0011 others(10): Show |
205 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*106C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 106 | chr2 | 27101168 | ||||||
| chr2:27101169 | C | T | 1 | a0001c0002t0008 | 2 | HG03195.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 6/6 | 105 | chr2 | 27101169 | ||||||
| chr2:27118886 | G | A | 1 | a0001c0002t0017 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/6 | 14520 | chr2 | 27118886 | ||||||
| chr2:27118906 | C | T | 1 | a0001c0001t0012 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/6 | 14540 | chr2 | 27118906 | ||||||
| chr2:27119090 | G | A | 1 | a0002c0003t0018 | 1 | HG02976.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-256C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/6 | chr2 | 27119090 | |||||||
| chr2:27119097 | C | T | 1 | a0001c0001t0011 | 1 | HG00673.hp2 | 5_prime_UTR_variant | MODIFIER | c.-263G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/6 | 14731 | chr2 | 27119097 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27102048 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.342+49T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 5/5 | chr2 | 27102048 | |||||||
| chr2:27102256 | C | T | 3 | a0001c0001t0001g0243 a0001c0002t0001g0126 a0001c0002t0002g0111 |
3 | HG01109.hp1 NA18522.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.218-35G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 4/5 | chr2 | 27102256 | |||||||
| chr2:27102273 | G | A | 2 | a0001c0001t0010g0168 a0001c0001t0010g0205 |
2 | HG01256.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.218-52C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 4/5 | chr2 | 27102273 | |||||||
| chr2:27102672 | T | C | 1 | a0001c0002t0002g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.81-81A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27102672 | |||||||
| chr2:27102857 | G | A | 1 | a0002c0003t0003g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81-266C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27102857 | |||||||
| chr2:27102969 | T | A | 108 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0060 others(105): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.81-378A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27102969 | |||||||
| chr2:27102976 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.81-385G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27102976 | |||||||
| chr2:27103199 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.81-608C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103199 | |||||||
| chr2:27103259 | C | T | 15 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0122 others(12): Show |
17 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.81-668G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103259 | |||||||
| chr2:27103367 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.81-776C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103367 | |||||||
| chr2:27103380 | C | CT | 166 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(163): Show |
179 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.81-790dupA | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103380 | |||||||
| chr2:27103380 | C | CTT | 107 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0060 others(104): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.81-791_81-790dupAA | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103380 | |||||||
| chr2:27103423 | A | G | 2 | a0001c0002t0002g0076 a0001c0002t0002g0083 |
2 | HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.81-832T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103423 | |||||||
| chr2:27103458 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0251 |
2 | HG01109.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.80+829G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103458 | |||||||
| chr2:27103506 | G | C | 1 | a0001c0002t0002g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80+781C>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103506 | |||||||
| chr2:27103518 | A | G | 2 | a0001c0004t0001g0293 a0001c0004t0016g0292 |
2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.80+769T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103518 | |||||||
| chr2:27103720 | C | A | 1 | a0001c0002t0001g0129 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.80+567G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103720 | |||||||
| chr2:27103737 | C | T | 5 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0001g0286 others(2): Show |
6 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+550G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103737 | |||||||
| chr2:27103852 | G | A | 1 | a0001c0011t0002g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80+435C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103852 | |||||||
| chr2:27103875 | C | T | 1 | a0001c0002t0008g0015 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80+412G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103875 | |||||||
| chr2:27103876 | G | A | 15 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0122 others(12): Show |
17 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.80+411C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103876 | |||||||
| chr2:27103907 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.80+380G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103907 | |||||||
| chr2:27103961 | C | T | 1 | a0001c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.80+326G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103961 | |||||||
| chr2:27103985 | GAACA | G | 6 | a0001c0001t0001g0054 a0001c0002t0002g0051 a0001c0002t0002g0052 others(3): Show |
6 | HG00280.hp2 HG00735.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.80+298_80+301delTG others(2): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27103985 | |||||||
| chr2:27104054 | C | T | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.80+233G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 2/5 | chr2 | 27104054 | |||||||
| chr2:27104404 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0223 a0001c0001t0001g0248 |
3 | HG01516.hp1 HG01517.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-11-27G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104404 | |||||||
| chr2:27104501 | T | C | 2 | a0001c0002t0002g0045 a0001c0002t0002g0046 |
2 | HG00140.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-11-124A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104501 | |||||||
| chr2:27104580 | G | A | 1 | a0002c0003t0002g0121 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11-203C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104580 | |||||||
| chr2:27104580 | G | C | 1 | a0001c0002t0007g0010 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11-203C>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104580 | |||||||
| chr2:27104603 | G | A | 1 | a0001c0002t0002g0047 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-11-226C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104603 | |||||||
| chr2:27104675 | G | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0180 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-11-298C>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104675 | |||||||
| chr2:27104776 | G | A | 2 | a0001c0002t0001g0089 a0001c0002t0001g0090 |
2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-11-399C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104776 | |||||||
| chr2:27104840 | T | G | 2 | a0001c0002t0002g0045 a0001c0002t0002g0046 |
2 | HG00140.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-11-463A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104840 | |||||||
| chr2:27104881 | G | A | 1 | a0001c0002t0002g0048 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-11-504C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104881 | |||||||
| chr2:27104889 | G | A | 4 | a0001c0002t0002g0059 a0001c0002t0002g0061 a0001c0002t0002g0062 others(1): Show |
4 | HG01074.hp2 HG02622.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-512C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27104889 | |||||||
| chr2:27105238 | C | T | 281 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-11-861G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27105238 | |||||||
| chr2:27105423 | C | T | 2 | a0002c0003t0009g0082 a0002c0003t0009g0088 |
2 | HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-11-1046G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27105423 | |||||||
| chr2:27105461 | T | A | 2 | a0001c0002t0002g0075 a0001c0002t0002g0096 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-11-1084A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27105461 | |||||||
| chr2:27105550 | T | TTTTTC | 278 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(275): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-11-1178_-11-1174d others(7): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27105550 | |||||||
| chr2:27105685 | T | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
168 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-11-1308A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27105685 | |||||||
| chr2:27105815 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-11-1438C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27105815 | |||||||
| chr2:27106095 | G | A | 2 | a0001c0002t0007g0010 a0001c0002t0007g0039 |
3 | HG03130.hp1 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-11-1718C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27106095 | |||||||
| chr2:27106411 | C | CCTGATAT others(7): Show |
1 | a0001c0002t0002g0067 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-11-2048_-11-2035d others(16): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27106411 | |||||||
| chr2:27106522 | A | C | 2 | a0001c0004t0001g0293 a0001c0004t0016g0292 |
2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11-2145T>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27106522 | |||||||
| chr2:27106575 | C | T | 4 | a0001c0002t0002g0059 a0001c0002t0002g0061 a0001c0002t0002g0062 others(1): Show |
4 | HG01074.hp2 HG02622.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-2198G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27106575 | |||||||
| chr2:27106608 | A | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(275): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-11-2231T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27106608 | |||||||
| chr2:27106655 | G | A | 3 | a0001c0002t0007g0010 a0001c0002t0007g0039 a0001c0004t0001g0040 |
4 | HG03130.hp1 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-2278C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27106655 | |||||||
| chr2:27106704 | C | T | 4 | a0001c0001t0001g0154 a0001c0001t0001g0160 a0001c0001t0001g0176 others(1): Show |
4 | HG03017.hp1 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-2327G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27106704 | |||||||
| chr2:27106800 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-11-2423A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27106800 | |||||||
| chr2:27107250 | A | ATTTGTTT others(3): Show |
1 | a0001c0002t0001g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-11-2874_-11-2873i others(12): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107250 | |||||||
| chr2:27107250 | A | ATTTGTTT others(8): Show |
13 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0122 others(10): Show |
15 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11-2874_-11-2873i others(17): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107250 | |||||||
| chr2:27107254 | T | G | 15 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0122 others(12): Show |
17 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-2877A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107254 | |||||||
| chr2:27107254 | T | TTTTTG | 86 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0002g0186 others(83): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-11-2882_-11-2878d others(7): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107254 | |||||||
| chr2:27107254 | T | TTTTTGTT others(3): Show |
180 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.-11-2887_-11-2878d others(12): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107254 | |||||||
| chr2:27107288 | T | C | 1 | a0001c0002t0002g0113 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-11-2911A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107288 | |||||||
| chr2:27107347 | C | T | 2 | a0002c0007t0002g0079 a0002c0007t0002g0095 |
2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-11-2970G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107347 | |||||||
| chr2:27107412 | G | A | 3 | a0001c0002t0002g0073 a0001c0004t0001g0293 a0001c0004t0016g0292 |
3 | HG02257.hp1 HG02300.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-11-3035C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107412 | |||||||
| chr2:27107485 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0175 a0001c0001t0001g0184 |
3 | NA18966.hp2 NA18968.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-11-3108G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107485 | |||||||
| chr2:27107578 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11-3201C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107578 | |||||||
| chr2:27107617 | G | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0203 a0001c0001t0001g0237 |
3 | HG01070.hp2 HG01071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-11-3240C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107617 | |||||||
| chr2:27107636 | T | A | 1 | a0001c0002t0007g0010 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11-3259A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107636 | |||||||
| chr2:27107637 | A | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0138 |
2 | HG02071.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-11-3260T>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107637 | |||||||
| chr2:27107663 | G | A | 1 | a0001c0002t0002g0047 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-11-3286C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107663 | |||||||
| chr2:27107933 | C | CA | 159 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(156): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.-11-3557dupT | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107933 | |||||||
| chr2:27107947 | A | AG | 5 | a0001c0001t0001g0153 a0003c0005t0001g0139 a0003c0005t0001g0163 others(2): Show |
5 | NA18944.hp2 NA18960.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-3571_-11-3570i others(3): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107947 | |||||||
| chr2:27107947 | A | G | 3 | a0001c0004t0001g0040 a0001c0004t0001g0069 a0001c0004t0001g0072 |
3 | HG01891.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-11-3570T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107947 | |||||||
| chr2:27107967 | T | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0159 a0001c0002t0002g0094 |
4 | HG02897.hp1 NA18982.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-3590A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27107967 | |||||||
| chr2:27108084 | G | A | 1 | a0001c0002t0002g0044 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-11-3707C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27108084 | |||||||
| chr2:27108234 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-11-3857C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27108234 | |||||||
| chr2:27108276 | T | A | 1 | a0001c0002t0002g0103 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-11-3899A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27108276 | |||||||
| chr2:27108395 | T | C | 1 | a0001c0002t0001g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11-4018A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27108395 | |||||||
| chr2:27108659 | T | C | 15 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0122 others(12): Show |
17 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-4282A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27108659 | |||||||
| chr2:27108688 | T | A | 1 | a0001c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11-4311A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27108688 | |||||||
| chr2:27108697 | T | TCAA | 277 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(274): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-11-4323_-11-4321d others(5): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27108697 | |||||||
| chr2:27108781 | C | A | 1 | a0001c0002t0008g0015 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-11-4404G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27108781 | |||||||
| chr2:27109113 | T | A | 1 | a0001c0001t0002g0186 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-11-4736A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109113 | |||||||
| chr2:27109126 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-11-4749A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109126 | |||||||
| chr2:27109298 | A | G | 280 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(277): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-11-4921T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109298 | |||||||
| chr2:27109371 | T | TA | 170 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(167): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-11-4995dupT | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109371 | |||||||
| chr2:27109371 | TA | T | 8 | a0001c0002t0002g0049 a0001c0002t0002g0059 a0001c0002t0002g0061 others(5): Show |
9 | HG01074.hp1 HG01074.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11-4995delT | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109371 | |||||||
| chr2:27109386 | AG | A | 22 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0017 others(19): Show |
43 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11-5010delC | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109386 | |||||||
| chr2:27109417 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-11-5040T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109417 | |||||||
| chr2:27109443 | A | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0239 |
2 | HG02109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-11-5066T>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109443 | |||||||
| chr2:27109491 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-11-5114C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109491 | |||||||
| chr2:27109567 | G | A | 281 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-11-5190C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109567 | |||||||
| chr2:27109640 | C | A | 4 | a0001c0002t0002g0003 a0001c0002t0002g0037 a0001c0002t0002g0067 others(1): Show |
9 | HG02083.hp1 HG02155.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11-5263G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109640 | |||||||
| chr2:27109675 | T | C | 1 | a0001c0002t0004g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11-5298A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109675 | |||||||
| chr2:27109885 | C | CA | 11 | a0001c0001t0001g0154 a0001c0001t0001g0204 a0001c0001t0001g0243 others(8): Show |
11 | HG01109.hp1 HG01168.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-5509dupT | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109885 | |||||||
| chr2:27109885 | C | CAA | 111 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0024 others(108): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.-11-5510_-11-5509d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109885 | |||||||
| chr2:27109885 | C | CAAA | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0027 others(44): Show |
52 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-11-5511_-11-5509d others(5): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109885 | |||||||
| chr2:27109885 | C | CAAAA | 8 | a0001c0001t0001g0141 a0001c0001t0001g0162 a0001c0001t0001g0174 others(5): Show |
8 | HG01074.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11-5512_-11-5509d others(6): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109885 | |||||||
| chr2:27109885 | CA | C | 81 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0002t0001g0090 others(78): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-11-5509delT | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109885 | |||||||
| chr2:27109885 | CAA | C | 6 | a0001c0002t0002g0020 a0001c0002t0004g0116 a0001c0002t0004g0119 others(3): Show |
9 | HG00733.hp2 HG01167.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11-5510_-11-5509d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109885 | |||||||
| chr2:27109901 | A | G | 76 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0002t0002g0001 others(73): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-11-5524T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27109901 | |||||||
| chr2:27110037 | A | G | 1 | a0001c0002t0002g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-5660T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110037 | |||||||
| chr2:27110245 | T | A | 15 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0122 others(12): Show |
17 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-5868A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110245 | |||||||
| chr2:27110246 | A | T | 2 | a0001c0001t0001g0151 a0001c0002t0002g0190 |
2 | HG02572.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-11-5869T>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110246 | |||||||
| chr2:27110313 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-5936C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110313 | |||||||
| chr2:27110406 | TAC | T | 279 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-11-6031_-11-6030d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110406 | |||||||
| chr2:27110577 | A | AAT | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0028 others(94): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.-11-6202_-11-6201d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110577 | |||||||
| chr2:27110577 | A | AATAT | 70 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(67): Show |
77 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.-11-6204_-11-6201d others(6): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110577 | |||||||
| chr2:27110638 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0267 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-11-6261A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110638 | |||||||
| chr2:27110685 | T | C | 1 | a0001c0002t0002g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-11-6308A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110685 | |||||||
| chr2:27110691 | C | T | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG00140.hp2 HG01433.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-6314G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110691 | |||||||
| chr2:27110774 | G | C | 1 | a0001c0002t0001g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-11-6397C>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110774 | |||||||
| chr2:27110836 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-11-6459C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110836 | |||||||
| chr2:27110892 | C | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0172 a0001c0001t0001g0201 others(6): Show |
11 | HG00558.hp2 HG00621.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11-6515G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110892 | |||||||
| chr2:27110904 | T | C | 280 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(277): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-11-6527A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27110904 | |||||||
| chr2:27111058 | A | G | 1 | a0001c0002t0002g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11-6681T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111058 | |||||||
| chr2:27111086 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-11-6709C>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111086 | |||||||
| chr2:27111097 | A | G | 280 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(277): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-11-6720T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111097 | |||||||
| chr2:27111100 | G | A | 2 | a0001c0002t0002g0018 a0001c0002t0002g0106 |
3 | HG00438.hp2 NA18988.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-11-6723C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111100 | |||||||
| chr2:27111471 | G | A | 166 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(163): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-11-7094C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111471 | |||||||
| chr2:27111472 | G | A | 1 | a0001c0002t0008g0015 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-11-7095C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111472 | |||||||
| chr2:27111549 | C | T | 3 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0043 |
5 | HG00733.hp2 HG01167.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-7172G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111549 | |||||||
| chr2:27111733 | GGGCCGGC others(6): Show |
G | 2 | a0001c0004t0001g0293 a0001c0004t0016g0292 |
2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-12+7100_-12+7112d others(15): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111733 | |||||||
| chr2:27111748 | G | A | 1 | a0001c0002t0007g0010 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-12+7098C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111748 | |||||||
| chr2:27111756 | C | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-12+7090G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111756 | |||||||
| chr2:27111768 | GGCCCCCG others(1): Show |
G | 5 | a0001c0001t0001g0141 a0001c0001t0001g0152 a0001c0001t0001g0156 others(2): Show |
5 | HG02647.hp1 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+7070_-12+7077d others(10): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111768 | |||||||
| chr2:27111803 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12+7043C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111803 | |||||||
| chr2:27111937 | G | T | 12 | a0001c0001t0001g0282 a0001c0002t0001g0089 a0001c0002t0001g0090 others(9): Show |
12 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12+6909C>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111937 | |||||||
| chr2:27111953 | C | A | 1 | a0001c0002t0001g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-12+6893G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111953 | |||||||
| chr2:27111956 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-12+6890C>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111956 | |||||||
| chr2:27111983 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-12+6863G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27111983 | |||||||
| chr2:27112029 | G | A | 3 | a0001c0002t0005g0013 a0001c0002t0005g0014 a0001c0002t0005g0043 |
5 | HG00733.hp2 HG01167.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+6817C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27112029 | |||||||
| chr2:27112032 | G | T | 80 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0291 others(77): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.-12+6814C>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27112032 | |||||||
| chr2:27112102 | C | T | 1 | a0001c0002t0002g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-12+6744G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27112102 | |||||||
| chr2:27112139 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-12+6707A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27112139 | |||||||
| chr2:27112205 | G | A | 1 | a0001c0002t0002g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-12+6641C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27112205 | |||||||
| chr2:27112669 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-12+6177T>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27112669 | |||||||
| chr2:27112718 | T | C | 76 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0291 others(73): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-12+6128A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27112718 | |||||||
| chr2:27112912 | G | A | 1 | a0001c0002t0002g0107 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-12+5934C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27112912 | |||||||
| chr2:27113109 | CAG | C | 22 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0122 others(19): Show |
27 | HG00639.hp1 HG00733.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.-12+5735_-12+5736d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113109 | |||||||
| chr2:27113269 | C | T | 1 | a0001c0004t0001g0293 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12+5577G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113269 | |||||||
| chr2:27113389 | A | G | 6 | a0001c0002t0002g0020 a0001c0002t0002g0068 a0001c0002t0004g0021 others(3): Show |
8 | HG00738.hp1 HG02922.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+5457T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113389 | |||||||
| chr2:27113418 | C | G | 1 | a0001c0001t0002g0186 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-12+5428G>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113418 | |||||||
| chr2:27113474 | T | G | 1 | a0001c0001t0001g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-12+5372A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113474 | |||||||
| chr2:27113508 | T | C | 102 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0291 others(99): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-12+5338A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113508 | |||||||
| chr2:27113539 | A | G | 1 | a0001c0002t0002g0102 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-12+5307T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113539 | |||||||
| chr2:27113564 | A | C | 92 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0291 others(89): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.-12+5282T>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113564 | |||||||
| chr2:27113635 | C | T | 29 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0291 others(26): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.-12+5211G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113635 | |||||||
| chr2:27113671 | GGTTCTCC others(48): Show |
G | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+5120_-12+5174d others(57): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113671 | |||||||
| chr2:27113797 | G | T | 1 | a0001c0002t0002g0044 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-12+5049C>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113797 | |||||||
| chr2:27113836 | C | A | 1 | a0001c0001t0001g0281 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-12+5010G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113836 | |||||||
| chr2:27113854 | C | T | 4 | a0001c0002t0002g0059 a0001c0002t0002g0061 a0001c0002t0002g0062 others(1): Show |
4 | HG01074.hp2 HG02622.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+4992G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113854 | |||||||
| chr2:27113902 | G | A | 1 | a0001c0001t0014g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-12+4944C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113902 | |||||||
| chr2:27113959 | C | A | 137 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0060 others(134): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.-12+4887G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113959 | |||||||
| chr2:27113975 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-12+4871G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113975 | |||||||
| chr2:27113977 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-12+4869A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113977 | |||||||
| chr2:27113990 | C | CT | 57 | a0001c0001t0001g0034 a0001c0001t0001g0140 a0001c0001t0001g0145 others(54): Show |
62 | HG00438.hp2 HG00621.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.-12+4855dupA | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113990 | |||||||
| chr2:27113990 | CT | C | 37 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0141 others(34): Show |
41 | HG00280.hp2 HG00639.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.-12+4855delA | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27113990 | |||||||
| chr2:27114006 | T | A | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+4840A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114006 | |||||||
| chr2:27114039 | G | T | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+4807C>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114039 | |||||||
| chr2:27114104 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-12+4742G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114104 | |||||||
| chr2:27114289 | G | A | 2 | a0002c0007t0002g0079 a0002c0007t0002g0095 |
2 | HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-12+4557C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114289 | |||||||
| chr2:27114391 | A | C | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+4455T>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114391 | |||||||
| chr2:27114392 | T | A | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+4454A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114392 | |||||||
| chr2:27114393 | C | T | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+4453G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114393 | |||||||
| chr2:27114456 | T | C | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+4390A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114456 | |||||||
| chr2:27114583 | C | A | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+4263G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114583 | |||||||
| chr2:27114649 | A | C | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+4197T>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114649 | |||||||
| chr2:27114770 | AG | A | 4 | a0001c0002t0002g0045 a0001c0002t0002g0056 a0001c0002t0002g0057 others(1): Show |
4 | HG00140.hp1 HG00642.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+4075delC | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114770 | |||||||
| chr2:27114821 | C | A | 5 | a0001c0002t0001g0122 a0001c0002t0001g0127 a0001c0002t0001g0129 others(2): Show |
5 | HG01106.hp2 HG01346.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+4025G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114821 | |||||||
| chr2:27114904 | T | G | 23 | a0001c0001t0001g0028 a0001c0001t0001g0276 a0001c0001t0001g0277 others(20): Show |
28 | HG00140.hp2 HG00733.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-12+3942A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114904 | |||||||
| chr2:27114904 | T | TTG | 7 | a0001c0001t0001g0184 a0001c0001t0001g0202 a0001c0001t0001g0229 others(4): Show |
7 | HG03688.hp2 NA18966.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12+3940_-12+3941d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114904 | |||||||
| chr2:27114987 | G | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0203 a0001c0001t0001g0237 |
3 | HG01070.hp2 HG01071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-12+3859C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27114987 | |||||||
| chr2:27115119 | T | G | 2 | a0001c0004t0001g0293 a0001c0004t0016g0292 |
2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-12+3727A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115119 | |||||||
| chr2:27115163 | A | AG | 8 | a0001c0001t0001g0028 a0001c0001t0001g0276 a0001c0001t0001g0277 others(5): Show |
9 | HG00140.hp2 HG01361.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+3682dupC | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115163 | |||||||
| chr2:27115237 | C | A | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+3609G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115237 | |||||||
| chr2:27115379 | T | C | 1 | a0002c0003t0018g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-12+3467A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115379 | |||||||
| chr2:27115415 | C | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0232 |
2 | NA19070.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-12+3431G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115415 | |||||||
| chr2:27115422 | T | C | 21 | a0001c0001t0001g0028 a0001c0001t0001g0276 a0001c0001t0001g0277 others(18): Show |
25 | HG00140.hp2 HG00733.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-12+3424A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115422 | |||||||
| chr2:27115424 | A | C | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+3422T>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115424 | |||||||
| chr2:27115471 | G | T | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+3375C>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115471 | |||||||
| chr2:27115714 | C | T | 7 | a0001c0002t0002g0059 a0001c0002t0002g0061 a0001c0002t0002g0062 others(4): Show |
9 | HG00733.hp2 HG01074.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+3132G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115714 | |||||||
| chr2:27115859 | A | C | 2 | a0001c0002t0002g0080 a0001c0002t0002g0081 |
2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-12+2987T>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27115859 | |||||||
| chr2:27116037 | AC | A | 101 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0291 others(98): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-12+2808delG | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116037 | |||||||
| chr2:27116098 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | NA18963.hp2 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-12+2748G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116098 | |||||||
| chr2:27116177 | A | C | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+2669T>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116177 | |||||||
| chr2:27116223 | C | A | 1 | a0001c0001t0001g0134 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-12+2623G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116223 | |||||||
| chr2:27116223 | C | CA | 98 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0164 others(95): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-12+2622dupT | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116223 | |||||||
| chr2:27116223 | C | CAA | 16 | a0001c0001t0001g0032 a0001c0002t0002g0016 a0001c0002t0002g0019 others(13): Show |
18 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12+2621_-12+2622d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116223 | |||||||
| chr2:27116223 | CA | C | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0002t0002g0059 others(4): Show |
7 | HG01074.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+2622delT | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116223 | |||||||
| chr2:27116240 | A | C | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+2606T>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116240 | |||||||
| chr2:27116241 | C | A | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+2605G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116241 | |||||||
| chr2:27116248 | C | T | 93 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0291 others(90): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-12+2598G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116248 | |||||||
| chr2:27116290 | G | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0245 a0001c0001t0001g0258 |
3 | HG01099.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-12+2556C>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116290 | |||||||
| chr2:27116363 | C | A | 1 | a0001c0002t0002g0073 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-12+2483G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116363 | |||||||
| chr2:27116398 | G | A | 2 | a0001c0002t0002g0011 a0001c0002t0002g0042 |
3 | HG00639.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-12+2448C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116398 | |||||||
| chr2:27116526 | A | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0276 a0001c0001t0001g0277 others(14): Show |
21 | HG00140.hp2 HG00733.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12+2320T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116526 | |||||||
| chr2:27116540 | A | G | 6 | a0001c0002t0002g0076 a0001c0002t0002g0077 a0001c0002t0004g0021 others(3): Show |
7 | HG00738.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+2306T>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116540 | |||||||
| chr2:27116574 | AT | A | 23 | a0001c0001t0001g0028 a0001c0001t0001g0276 a0001c0001t0001g0277 others(20): Show |
27 | HG00140.hp2 HG00733.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-12+2271delA | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116574 | |||||||
| chr2:27116673 | G | A | 3 | a0002c0003t0002g0120 a0002c0003t0002g0121 a0002c0003t0018g0295 |
3 | HG01109.hp2 HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-12+2173C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116673 | |||||||
| chr2:27116871 | T | TCTCTCTC others(6): Show |
1 | a0001c0001t0001g0267 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-12+1974_-12+1975i others(15): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTC | 8 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0184 others(5): Show |
9 | HG01071.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12+1973_-12+1974d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCCCTCT others(29): Show |
1 | a0005c0010t0002g0074 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-12+1974_-12+1975i others(38): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTC | 6 | a0001c0001t0001g0026 a0001c0001t0001g0143 a0001c0001t0001g0187 others(3): Show |
7 | HG00609.hp1 HG01081.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12+1971_-12+1974d others(6): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTC | 8 | a0001c0001t0001g0144 a0001c0001t0001g0191 a0001c0001t0001g0193 others(5): Show |
8 | HG00099.hp2 HG02738.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12+1969_-12+1974d others(8): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(1): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0196 a0001c0001t0001g0263 others(1): Show |
5 | HG01346.hp2 HG02698.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+1967_-12+1974d others(10): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(3): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03540.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-12+1965_-12+1974d others(12): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(5): Show |
1 | a0001c0001t0001g0145 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-12+1963_-12+1974d others(14): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(7): Show |
3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG00558.hp2 HG03654.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-12+1961_-12+1974d others(16): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(11): Show |
2 | a0001c0001t0001g0204 a0001c0001t0010g0205 |
2 | HG01256.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-12+1957_-12+1974d others(20): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(13): Show |
1 | a0001c0004t0016g0292 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-12+1955_-12+1974d others(22): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(15): Show |
4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0002c0003t0003g0208 others(1): Show |
4 | HG00738.hp2 HG01169.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+1953_-12+1974d others(24): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(17): Show |
3 | a0001c0001t0001g0209 a0001c0001t0001g0272 a0001c0001t0006g0210 |
3 | HG01175.hp2 HG01261.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-12+1951_-12+1974d others(26): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(19): Show |
1 | a0001c0002t0002g0101 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-12+1974_-12+1975i others(28): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(27): Show |
1 | a0001c0002t0002g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-12+1974_-12+1975i others(36): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(19): Show |
3 | a0001c0001t0001g0212 a0001c0001t0001g0268 a0001c0004t0001g0211 |
3 | HG00323.hp2 NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-12+1949_-12+1974d others(28): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(21): Show |
3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0006g0273 |
3 | HG00735.hp1 HG01516.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-12+1947_-12+1974d others(30): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(23): Show |
4 | a0001c0001t0001g0216 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG00323.hp1 HG00621.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+1945_-12+1974d others(32): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(25): Show |
3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0002t0017g0294 |
3 | HG02738.hp1 NA18979.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-12+1943_-12+1974d others(34): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(27): Show |
4 | a0001c0001t0001g0146 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG00673.hp1 HG01175.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+1941_-12+1974d others(36): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(29): Show |
5 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG01516.hp1 HG02080.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1939_-12+1974d others(38): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(31): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0227 a0001c0004t0001g0226 |
3 | HG04184.hp2 NA18968.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-12+1937_-12+1974d others(40): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(33): Show |
1 | a0001c0001t0001g0009 | 3 | NA19007.hp2 NA19064.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-12+1935_-12+1974d others(42): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(37): Show |
2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG00544.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-12+1931_-12+1974d others(46): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(41): Show |
2 | a0001c0001t0001g0230 a0001c0001t0011g0030 |
2 | HG00673.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-12+1927_-12+1974d others(50): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(43): Show |
2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | NA18999.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-12+1925_-12+1974d others(52): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(45): Show |
1 | a0001c0001t0001g0233 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-12+1923_-12+1974d others(54): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | T | TTCTCTCT others(103): Show |
1 | a0001c0004t0001g0293 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12+1974_-12+1975i others(112): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTC | T | 12 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0167 others(9): Show |
12 | HG00621.hp2 HG01257.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+1973_-12+1974d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTC | T | 18 | a0001c0001t0001g0036 a0001c0001t0001g0134 a0001c0001t0001g0137 others(15): Show |
18 | HG01258.hp2 HG01346.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12+1971_-12+1974d others(6): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTCTC | T | 14 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0155 others(11): Show |
14 | HG00639.hp1 HG01123.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12+1969_-12+1974d others(8): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTCTCT others(1): Show |
T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0153 a0001c0001t0001g0154 others(5): Show |
10 | HG00735.hp2 HG01884.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+1967_-12+1974d others(10): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTCTCT others(3): Show |
T | 10 | a0001c0001t0001g0152 a0001c0001t0001g0282 a0001c0002t0001g0122 others(7): Show |
13 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12+1965_-12+1974d others(12): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTCTCT others(5): Show |
T | 9 | a0001c0001t0001g0291 a0001c0002t0001g0022 a0001c0002t0002g0012 others(6): Show |
11 | HG01074.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+1963_-12+1974d others(14): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTCTCT others(7): Show |
T | 10 | a0001c0001t0001g0151 a0001c0002t0002g0011 a0001c0002t0002g0044 others(7): Show |
13 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12+1961_-12+1974d others(16): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTCTCT others(9): Show |
T | 4 | a0001c0002t0002g0041 a0001c0002t0002g0042 a0001c0002t0005g0013 others(1): Show |
5 | HG00639.hp2 HG01358.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1959_-12+1974d others(18): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTCTCT others(11): Show |
T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0136 a0001c0001t0001g0150 others(6): Show |
10 | HG00140.hp2 HG01433.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+1957_-12+1974d others(20): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTCTCT others(15): Show |
T | 1 | a0001c0001t0001g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-12+1953_-12+1974d others(24): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116871 | TTCTCTCT others(17): Show |
T | 2 | a0002c0003t0002g0121 a0002c0003t0018g0295 |
2 | HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-12+1951_-12+1974d others(26): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116871 | |||||||
| chr2:27116872 | T | TCTCTCTC others(17): Show |
1 | a0001c0002t0002g0002 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-12+1973_-12+1974i others(26): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116872 | |||||||
| chr2:27116874 | T | C | 1 | a0001c0002t0002g0003 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-12+1972A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116874 | |||||||
| chr2:27116892 | T | TCTCTCTC others(12): Show |
1 | a0001c0001t0001g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-12+1935_-12+1953d others(21): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116892 | |||||||
| chr2:27116900 | TCTCTCTC others(16): Show |
T | 1 | a0002c0003t0002g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-12+1923_-12+1945d others(25): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116900 | |||||||
| chr2:27116910 | T | TCTCTCTC others(38): Show |
1 | a0001c0001t0001g0172 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-12+1935_-12+1936i others(47): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116910 | |||||||
| chr2:27116912 | TCTCTCTC others(4): Show |
T | 2 | a0001c0002t0002g0002 a0001c0002t0002g0055 |
2 | HG00597.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-12+1923_-12+1933d others(13): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116912 | |||||||
| chr2:27116913 | CTCTCTCT others(6): Show |
C | 1 | a0001c0002t0002g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12+1920_-12+1932d others(15): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116913 | |||||||
| chr2:27116916 | TCTCTCTC | T | 3 | a0001c0001t0001g0054 a0001c0002t0004g0021 a0001c0002t0004g0119 |
4 | HG00738.hp1 HG01192.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+1923_-12+1929d others(9): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116916 | |||||||
| chr2:27116919 | CTCTCT | C | 3 | a0001c0001t0001g0008 a0001c0002t0001g0133 a0003c0005t0001g0173 |
3 | HG01106.hp2 HG02071.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-12+1922_-12+1926d others(7): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116919 | |||||||
| chr2:27116921 | C | T | 2 | a0001c0002t0002g0075 a0001c0002t0002g0096 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-12+1925G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116921 | |||||||
| chr2:27116923 | C | CTCACTTC others(20): Show |
1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(29): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(4): Show |
1 | a0001c0002t0002g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(13): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(6): Show |
1 | a0001c0002t0002g0001 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(15): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(10): Show |
2 | a0001c0002t0002g0001 a0001c0002t0002g0103 |
2 | HG01106.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(19): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(12): Show |
1 | a0002c0007t0002g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(21): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(14): Show |
3 | a0001c0002t0002g0003 a0001c0002t0002g0016 a0001c0002t0002g0109 |
3 | HG02148.hp1 HG03516.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(23): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(16): Show |
4 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0081 others(1): Show |
4 | HG02897.hp1 HG03239.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(25): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(18): Show |
4 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0076 others(1): Show |
4 | HG02083.hp1 HG02145.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(27): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(22): Show |
3 | a0001c0002t0002g0102 a0001c0002t0002g0106 a0001c0002t0002g0111 |
3 | HG00597.hp1 NA18956.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(31): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(24): Show |
1 | a0001c0002t0002g0004 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(33): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(26): Show |
5 | a0001c0002t0002g0002 a0001c0002t0002g0077 a0001c0002t0002g0085 others(2): Show |
5 | HG01928.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(35): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(28): Show |
2 | a0001c0002t0002g0001 a0001c0002t0013g0092 |
2 | HG01358.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(37): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(30): Show |
2 | a0001c0002t0002g0078 a0001c0002t0002g0087 |
2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(39): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(32): Show |
1 | a0001c0002t0002g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(41): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(34): Show |
1 | a0001c0002t0002g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(43): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(33): Show |
1 | a0001c0002t0002g0073 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(42): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(31): Show |
1 | a0001c0002t0002g0113 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(40): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(29): Show |
1 | a0001c0002t0002g0067 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(38): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(27): Show |
3 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0002c0003t0009g0082 |
3 | HG02886.hp1 NA18944.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(36): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(25): Show |
5 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0091 others(2): Show |
5 | HG00099.hp1 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(34): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(23): Show |
5 | a0001c0002t0002g0001 a0001c0002t0002g0017 a0001c0002t0002g0057 others(2): Show |
6 | HG00642.hp2 HG00741.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(32): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(21): Show |
2 | a0001c0002t0002g0016 a0001c0009t0002g0084 |
2 | HG02015.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(30): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(19): Show |
6 | a0001c0002t0002g0038 a0001c0002t0002g0070 a0001c0002t0002g0083 others(3): Show |
6 | HG00741.hp1 HG01891.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(28): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(17): Show |
8 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
11 | HG00438.hp2 HG00544.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(26): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(15): Show |
3 | a0001c0002t0002g0001 a0001c0002t0002g0019 a0001c0002t0002g0071 |
3 | HG03017.hp2 NA19065.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(24): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(13): Show |
2 | a0001c0002t0002g0002 a0001c0002t0002g0018 |
2 | NA19068.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(22): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(11): Show |
1 | a0001c0002t0002g0110 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(20): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(9): Show |
1 | a0001c0002t0002g0001 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(18): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(7): Show |
1 | a0001c0002t0002g0001 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(16): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(5): Show |
2 | a0001c0002t0002g0002 a0001c0002t0002g0003 |
2 | HG02155.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-12+1922_-12+1923i others(14): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | CTCTCTCT others(3): Show |
1 | a0001c0002t0002g0112 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-12+1922_-12+1923i others(12): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116923 | C | T | 60 | a0001c0001t0001g0028 a0001c0001t0001g0276 a0001c0001t0001g0277 others(57): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-12+1923G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116923 | |||||||
| chr2:27116924 | T | TC | 6 | a0001c0001t0001g0032 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
6 | HG01070.hp2 HG01255.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(3): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(2): Show |
3 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 |
3 | HG02895.hp2 HG03704.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(11): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(6): Show |
1 | a0001c0001t0001g0241 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-12+1921_-12+1922i others(15): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(8): Show |
1 | a0001c0001t0001g0242 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-12+1921_-12+1922i others(17): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(14): Show |
2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG01109.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(23): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(16): Show |
3 | a0001c0001t0001g0245 a0001c0002t0002g0114 a0004c0006t0002g0066 |
3 | HG01168.hp2 HG01993.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(25): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(18): Show |
1 | a0001c0001t0001g0246 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-12+1921_-12+1922i others(27): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(20): Show |
3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG03239.hp2 NA18955.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(29): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(22): Show |
4 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG03490.hp1 HG03490.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(31): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(24): Show |
1 | a0001c0001t0006g0254 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-12+1921_-12+1922i others(33): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(26): Show |
2 | a0001c0001t0001g0255 a0001c0002t0002g0115 |
2 | NA18950.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(35): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(28): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG01070.hp1 HG01517.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(37): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(30): Show |
2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG00280.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(39): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(32): Show |
3 | a0001c0001t0001g0149 a0001c0001t0001g0260 a0001c0001t0001g0266 |
3 | HG02155.hp1 HG04228.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-12+1921_-12+1922i others(41): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116924 | T | TCTCTCTC others(34): Show |
1 | a0001c0004t0015g0261 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-12+1921_-12+1922i others(43): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116924 | |||||||
| chr2:27116925 | T | C | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG00323.hp1 HG01123.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+1921A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116925 | |||||||
| chr2:27116926 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG01258.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-12+1920A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116926 | |||||||
| chr2:27116928 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-12+1918A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116928 | |||||||
| chr2:27116960 | T | G | 23 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0017 others(20): Show |
44 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-12+1886A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116960 | |||||||
| chr2:27116974 | G | A | 8 | a0001c0001t0001g0268 a0001c0002t0002g0020 a0001c0002t0002g0068 others(5): Show |
10 | HG00738.hp1 HG01884.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+1872C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27116974 | |||||||
| chr2:27117192 | T | A | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+1654A>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117192 | |||||||
| chr2:27117209 | C | A | 15 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0122 others(12): Show |
17 | HG00639.hp1 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12+1637G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117209 | |||||||
| chr2:27117532 | G | C | 1 | a0001c0001t0001g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-12+1314C>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117532 | |||||||
| chr2:27117639 | G | A | 3 | a0001c0002t0007g0010 a0001c0002t0007g0039 a0001c0004t0001g0040 |
4 | HG03130.hp1 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+1207C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117639 | |||||||
| chr2:27117705 | A | AT | 22 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
22 | HG00621.hp2 HG01074.hp2 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12+1140dupA | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117705 | |||||||
| chr2:27117705 | A | ATT | 12 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0134 others(9): Show |
15 | HG00733.hp2 HG01167.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-12+1139_-12+1140d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117705 | |||||||
| chr2:27117705 | A | ATTT | 30 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0276 others(27): Show |
35 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.-12+1138_-12+1140d others(5): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117705 | |||||||
| chr2:27117705 | AT | A | 15 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(12): Show |
15 | HG00741.hp1 HG01071.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+1140delA | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117705 | |||||||
| chr2:27117705 | ATT | A | 72 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0089 others(69): Show |
108 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-12+1139_-12+1140d others(4): Show |
CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117705 | |||||||
| chr2:27117729 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-12+1117C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117729 | |||||||
| chr2:27117951 | T | C | 131 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0060 others(128): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-12+895A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27117951 | |||||||
| chr2:27118148 | C | T | 1 | a0001c0002t0002g0038 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-12+698G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118148 | |||||||
| chr2:27118171 | T | C | 18 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0122 others(15): Show |
20 | HG00639.hp1 HG01106.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12+675A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118171 | |||||||
| chr2:27118195 | A | T | 122 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0291 others(119): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-12+651T>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118195 | |||||||
| chr2:27118197 | C | A | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+649G>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118197 | |||||||
| chr2:27118213 | A | T | 1 | a0001c0002t0002g0037 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-12+633T>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118213 | |||||||
| chr2:27118233 | T | G | 1 | a0001c0001t0001g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-12+613A>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118233 | |||||||
| chr2:27118277 | C | G | 1 | a0002c0003t0018g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-12+569G>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118277 | |||||||
| chr2:27118336 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | NA18941.hp2 NA18963.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+510G>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118336 | |||||||
| chr2:27118455 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA18951.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-12+391C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118455 | |||||||
| chr2:27118469 | G | A | 1 | a0001c0002t0001g0290 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-12+377C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118469 | |||||||
| chr2:27118521 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-12+325C>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118521 | |||||||
| chr2:27118784 | C | G | 1 | a0001c0001t0001g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-12+62G>C | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118784 | |||||||
| chr2:27118787 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-12+59A>G | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118787 | |||||||
| chr2:27118788 | G | T | 1 | a0001c0001t0001g0032 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-12+58C>A | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118788 | |||||||
| chr2:27118829 | G | A | 2 | a0001c0004t0001g0293 a0001c0004t0016g0292 |
2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-12+17C>T | CGREF1 | ENSG00000138028.17 | transcript | ENST00000402394.6 | protein_coding | 1/5 | chr2 | 27118829 |