Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1408 |
| ensemblid | ENSG00000121671.12 |
| hgncid | 2385 |
| symbol | CRY2 |
| name | cryptochrome circadian regulator 2 |
| refseq_nuc | NM_021117.5 |
| refseq_prot | NP_066940.3 |
| ensembl_nuc | ENST00000616080.2 |
| ensembl_prot | ENSP00000484684.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 45847475 |
| end | 45883244 |
| strand | + |
| ver | v1.2 |
| region | chr11:45847475-45883244 |
| region5000 | chr11:45842475-45888244 |
| regionname0 | CRY2_chr11_45847475_45883244 |
| regionname5000 | CRY2_chr11_45842475_45888244 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1779 | 360 | 88 | 65 | 147 | 16 | 42 | CRY2_chr11_45842475_45888244 | CRY2 | ATGGC others(1774): Show |
chr11 | 45842475 | 45888244 | ||
| a0001c0002 | 0/0 | 1779 | 4 | 4 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | ATGGC others(1774): Show |
chr11 | 45842475 | 45888244 | ||
| a0001c0003 | 0/0 | 1779 | 3 | 2 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | ATGGC others(1774): Show |
chr11 | 45842475 | 45888244 | ||
| a0001c0004 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | ATGGC others(1774): Show |
chr11 | 45842475 | 45888244 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4131 | 92 | 12 | 26 | 39 | 6 | 9 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0002 | 1/0 | 4131 | 76 | 9 | 10 | 50 | 0 | 6 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0003 | 0/0 | 4133 | 50 | 20 | 11 | 14 | 2 | 3 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4128): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0004 | 0/1 | 4133 | 47 | 0 | 7 | 31 | 3 | 5 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4128): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0005 | 0/0 | 4133 | 12 | 12 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4128): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0006 | 0/0 | 4133 | 12 | 2 | 5 | 0 | 4 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4128): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0007 | 0/0 | 4131 | 11 | 11 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0008 | 0/0 | 4131 | 9 | 3 | 4 | 1 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0009 | 0/0 | 4131 | 8 | 0 | 0 | 1 | 0 | 7 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0010 | 0/0 | 4131 | 8 | 8 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0011 | 0/0 | 4131 | 6 | 0 | 0 | 2 | 1 | 3 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0012 | 0/0 | 4135 | 5 | 0 | 2 | 3 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4130): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0013 | 0/0 | 4135 | 2 | 0 | 0 | 2 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4130): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0014 | 0/0 | 4131 | 2 | 0 | 0 | 0 | 0 | 2 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0015 | 0/0 | 4133 | 2 | 0 | 0 | 0 | 0 | 2 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4128): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0016 | 0/0 | 4131 | 2 | 2 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0017 | 0/0 | 4135 | 2 | 2 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4130): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0018 | 0/0 | 4133 | 2 | 2 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4128): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0019 | 0/0 | 4131 | 2 | 0 | 0 | 2 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0020 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0021 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4139): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0022 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0023 | 0/0 | 4131 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0024 | 0/0 | 4131 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0025 | 0/0 | 4135 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4130): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0026 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0027 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0028 | 0/0 | 4131 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0001t0029 | 0/0 | 4131 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0002t0002 | 0/0 | 4131 | 3 | 3 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| a0001c0002t0003 | 0/0 | 4133 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4128): Show |
chr11 | 45842475 | 45888244 |
| a0001c0003t0003 | 0/0 | 4133 | 2 | 1 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4128): Show |
chr11 | 45842475 | 45888244 |
| a0001c0003t0013 | 0/0 | 4135 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4130): Show |
chr11 | 45842475 | 45888244 |
| a0001c0004t0002 | 0/0 | 4131 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | AGCAG others(4126): Show |
chr11 | 45842475 | 45888244 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 36 | 2 | 10 | 17 | 4 | 3 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0002 | 0/0 | 14 | 0 | 1 | 10 | 0 | 3 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0005 | 1/0 | 6 | 3 | 2 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0018 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0008 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0005g0004 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0006g0010 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0006g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0007g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0007g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0008g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0009g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0009g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0009g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0010g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0010g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0010g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0011g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0011g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0011g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0012g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0012g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0012g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0012g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0013g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0014g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0015g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0015g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0016g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0017g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0018g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0018g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0019g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0019g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0020g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0021g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0022g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0023g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0024g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0025g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0026g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0027g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0028g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0001t0029g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0003t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0003t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0003t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| a0001c0004t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | GBR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00140 | hp1 | a0001 | c0001 | t0011 | g0037 | EUR | GBR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0015 | EUR | FIN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0086 | EUR | FIN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0075 | EUR | FIN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0010 | EUR | FIN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0105 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0214 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0055 | AMR | PUR | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0145 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0015 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0143 | EUR | IBS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0010 | EUR | IBS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01891 | hp1 | a0001 | c0001 | t0021 | g0079 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0175 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0182 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02083 | hp2 | a0001 | c0001 | t0029 | g0126 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0177 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02148 | hp2 | a0001 | c0001 | t0012 | g0190 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CDX | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | CDX | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0135 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02293 | hp1 | a0001 | c0001 | t0012 | g0191 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0140 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02602 | hp2 | a0001 | c0001 | t0009 | g0064 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0015 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02698 | hp1 | a0001 | c0001 | t0011 | g0037 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0104 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0012 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02809 | hp1 | a0001 | c0001 | t0026 | g0139 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02818 | hp1 | a0001 | c0001 | t0022 | g0176 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0129 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0149 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0142 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0152 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0106 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02922 | hp2 | a0001 | c0003 | t0003 | g0024 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02965 | hp1 | a0001 | c0001 | t0018 | g0060 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0098 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0147 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03017 | hp2 | a0001 | c0001 | t0009 | g0178 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03041 | hp1 | a0001 | c0001 | t0017 | g0099 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0141 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0016 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03139 | hp1 | a0001 | c0001 | t0027 | g0036 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0150 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03453 | hp2 | a0001 | c0003 | t0013 | g0024 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03491 | hp1 | a0001 | c0001 | t0015 | g0072 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03492 | hp2 | a0001 | c0001 | t0015 | g0082 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0146 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0016 | AFR | ESN | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03654 | hp1 | a0001 | c0001 | t0028 | g0066 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03654 | hp2 | a0001 | c0001 | t0023 | g0001 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03669 | hp1 | a0001 | c0001 | t0024 | g0001 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03669 | hp2 | a0001 | c0001 | t0009 | g0025 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | STU | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03704 | hp2 | a0001 | c0001 | t0014 | g0002 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03834 | hp1 | a0001 | c0001 | t0009 | g0025 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03942 | hp1 | a0001 | c0001 | t0009 | g0065 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0026 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | BEB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG04199 | hp1 | a0001 | c0001 | t0014 | g0002 | SAS | STU | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG04199 | hp2 | a0001 | c0001 | t0011 | g0133 | SAS | STU | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG04204 | hp2 | a0001 | c0001 | t0009 | g0063 | SAS | STU | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | STU | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0151 | AFR | YRI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | YRI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0130 | AFR | YRI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18957 | hp1 | a0001 | c0001 | t0025 | g0172 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18960 | hp2 | a0001 | c0001 | t0012 | g0022 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18964 | hp1 | a0001 | c0001 | t0013 | g0041 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18967 | hp2 | a0001 | c0001 | t0019 | g0034 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18973 | hp1 | a0001 | c0001 | t0019 | g0115 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18978 | hp1 | a0001 | c0001 | t0012 | g0185 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18978 | hp2 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18980 | hp1 | a0001 | c0001 | t0009 | g0026 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18984 | hp1 | a0001 | c0001 | t0012 | g0022 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18985 | hp2 | a0001 | c0004 | t0002 | g0110 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18995 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | LWK | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | LWK | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19066 | hp1 | a0001 | c0001 | t0013 | g0041 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | YRI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0016 | AFR | ASW | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | TSI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0074 | EUR | TSI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0148 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02559 | hp1 | a0001 | c0001 | t0018 | g0059 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0061 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | MSL | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | USA | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | USA | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | USA | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | USA | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | LWK | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0073 | REF | REF | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0005 | REF | REF | CRY2_chr11_45842475_45888244 | CRY2 | chr11 | 45842475 | 45888244 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45860977 | C | T | 1 | a0001c0003 | 3 | HG01243.hp2 HG02922.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.597C>T | p.Ala199Ala | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 4/12 | 613/4131 | 597/1782 | 199/593 | chr11 | 45860977 | |||
| chr11:45867677 | C | T | 1 | a0001c0002 | 4 | HG02258.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.807C>T | p.Gly269Gly | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/12 | 823/4131 | 807/1782 | 269/593 | chr11 | 45867677 | |||
| chr11:45872171 | C | G | 1 | a0001c0004 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.1722C>G | p.Leu574Leu | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/12 | 1738/4131 | 1722/1782 | 574/593 | chr11 | 45872171 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45880932 | G | A | 1 | a0001c0001t0014 | 2 | HG03704.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*21G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 8701 | chr11 | 45880932 | ||||||
| chr11:45881513 | C | T | 1 | a0001c0001t0010 | 8 | HG02486.hp2 HG02886.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*602C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9282 | chr11 | 45881513 | ||||||
| chr11:45881594 | C | G | 1 | a0001c0001t0029 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*683C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9363 | chr11 | 45881594 | ||||||
| chr11:45881601 | G | A | 1 | a0001c0001t0020 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*690G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9370 | chr11 | 45881601 | ||||||
| chr11:45881643 | A | G | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(1): Show |
43 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*732A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9412 | chr11 | 45881643 | ||||||
| chr11:45881705 | C | G | 2 | a0001c0001t0009 a0001c0001t0028 |
9 | HG02602.hp2 HG03017.hp2 HG03654.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*794C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9474 | chr11 | 45881705 | ||||||
| chr11:45881751 | T | TGAAGGGG others(4): Show |
1 | a0001c0001t0021 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842_*852dupAAGGGG others(5): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9533 | INFO_REALIGN_3_PRIME | chr11 | 45881751 | |||||
| chr11:45881782 | A | C | 1 | a0001c0001t0027 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*871A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9551 | chr11 | 45881782 | ||||||
| chr11:45881809 | G | A | 1 | a0001c0001t0015 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*898G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9578 | chr11 | 45881809 | ||||||
| chr11:45881989 | C | G | 1 | a0001c0001t0019 | 2 | NA18967.hp2 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1078C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9758 | chr11 | 45881989 | ||||||
| chr11:45882043 | A | G | 1 | a0001c0001t0026 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1132A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9812 | chr11 | 45882043 | ||||||
| chr11:45882062 | A | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(12): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*1151A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9831 | chr11 | 45882062 | ||||||
| chr11:45882076 | C | T | 1 | a0001c0001t0025 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1165C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 9845 | chr11 | 45882076 | ||||||
| chr11:45882263 | A | AGT | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(6): Show |
128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1368_*1369dupTG | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10050 | INFO_REALIGN_3_PRIME | chr11 | 45882263 | |||||
| chr11:45882263 | A | AGTGT | 4 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0025 others(1): Show |
6 | HG02970.hp1 HG03041.hp1 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1366_*1369dupTGTG | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10050 | INFO_REALIGN_3_PRIME | chr11 | 45882263 | |||||
| chr11:45882345 | C | T | 1 | a0001c0001t0024 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1434C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10114 | chr11 | 45882345 | ||||||
| chr11:45882370 | G | GCCTC | 1 | a0001c0001t0012 | 5 | HG02148.hp2 HG02293.hp1 NA18960.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1462_*1463insCCCT | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10143 | INFO_REALIGN_3_PRIME | chr11 | 45882370 | |||||
| chr11:45882616 | A | G | 1 | a0001c0001t0023 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1705A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10385 | chr11 | 45882616 | ||||||
| chr11:45882626 | G | A | 1 | a0001c0001t0003 | 5 | HG01261.hp1 HG01496.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1715G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10395 | chr11 | 45882626 | ||||||
| chr11:45882869 | C | A | 1 | a0001c0001t0018 | 2 | HG02559.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1958C>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10638 | chr11 | 45882869 | ||||||
| chr11:45882923 | A | G | 2 | a0001c0001t0016 a0001c0001t0022 |
3 | HG01891.hp2 HG02145.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2012A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10692 | chr11 | 45882923 | ||||||
| chr11:45882926 | T | C | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(19): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*2015T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10695 | chr11 | 45882926 | ||||||
| chr11:45882971 | C | T | 1 | a0001c0001t0028 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2060C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10740 | chr11 | 45882971 | ||||||
| chr11:45883064 | G | C | 1 | a0001c0001t0022 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2153G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 12/12 | 10833 | chr11 | 45883064 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45847824 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.215+119G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45847824 | |||||||
| chr11:45847894 | G | A | 8 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(5): Show |
8 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.215+189G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45847894 | |||||||
| chr11:45848067 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.215+362C>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848067 | |||||||
| chr11:45848107 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.215+402G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848107 | |||||||
| chr11:45848330 | T | G | 11 | a0001c0001t0005g0004 a0001c0001t0005g0061 a0001c0001t0005g0062 others(8): Show |
22 | HG02559.hp1 HG02559.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.215+625T>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848330 | |||||||
| chr11:45848388 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.215+683C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848388 | |||||||
| chr11:45848391 | G | A | 3 | a0001c0001t0002g0013 a0001c0001t0002g0067 a0001c0001t0002g0068 |
5 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.215+686G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848391 | |||||||
| chr11:45848626 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(50): Show |
100 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.215+921A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848626 | |||||||
| chr11:45848633 | A | G | 3 | a0001c0001t0016g0175 a0001c0001t0016g0177 a0001c0001t0022g0176 |
3 | HG01891.hp2 HG02145.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.215+928A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848633 | |||||||
| chr11:45848755 | G | A | 5 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(2): Show |
5 | HG01261.hp1 HG01496.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+1050G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848755 | |||||||
| chr11:45848861 | G | A | 1 | a0001c0001t0009g0178 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.215+1156G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848861 | |||||||
| chr11:45848992 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215+1287T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45848992 | |||||||
| chr11:45849076 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.215+1371C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849076 | |||||||
| chr11:45849192 | T | C | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.215+1487T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849192 | |||||||
| chr11:45849261 | G | A | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.215+1556G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849261 | |||||||
| chr11:45849520 | A | T | 32 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(29): Show |
49 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.215+1815A>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849520 | |||||||
| chr11:45849617 | A | G | 1 | a0001c0001t0004g0032 | 2 | HG02738.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.215+1912A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849617 | |||||||
| chr11:45849622 | A | AT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(63): Show |
113 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.215+1932dupT | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 45849622 | ||||||
| chr11:45849622 | A | ATT | 30 | a0001c0001t0001g0169 a0001c0001t0003g0011 a0001c0001t0003g0018 others(27): Show |
46 | HG00099.hp2 HG00733.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.215+1931_215+1932d others(4): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 45849622 | ||||||
| chr11:45849622 | AT | A | 9 | a0001c0001t0002g0067 a0001c0001t0002g0100 a0001c0001t0002g0101 others(6): Show |
9 | HG01069.hp1 HG01168.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+1932delT | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 45849622 | ||||||
| chr11:45849644 | G | A | 43 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0013 others(40): Show |
72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.215+1939G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849644 | |||||||
| chr11:45849681 | C | T | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.215+1976C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849681 | |||||||
| chr11:45849703 | C | G | 14 | a0001c0001t0006g0147 a0001c0001t0007g0007 a0001c0001t0007g0017 others(11): Show |
23 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.215+1998C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849703 | |||||||
| chr11:45849797 | A | G | 6 | a0001c0001t0006g0010 a0001c0001t0006g0015 a0001c0001t0006g0105 others(3): Show |
11 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.215+2092A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849797 | |||||||
| chr11:45849952 | C | A | 1 | a0001c0001t0011g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.215+2247C>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849952 | |||||||
| chr11:45849966 | G | C | 1 | a0001c0001t0016g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215+2261G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849966 | |||||||
| chr11:45849968 | G | T | 14 | a0001c0001t0006g0147 a0001c0001t0007g0007 a0001c0001t0007g0017 others(11): Show |
23 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.215+2263G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849968 | |||||||
| chr11:45849996 | G | C | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.215+2291G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849996 | |||||||
| chr11:45849999 | T | A | 3 | a0001c0001t0002g0036 a0001c0001t0002g0132 a0001c0001t0027g0036 |
3 | HG03139.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.215+2294T>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45849999 | |||||||
| chr11:45850008 | G | GT | 6 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0003g0174 others(3): Show |
6 | HG02970.hp1 HG03041.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+2318dupT | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 45850008 | ||||||
| chr11:45850008 | GT | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(114): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.215+2318delT | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 45850008 | ||||||
| chr11:45850014 | T | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(45): Show |
92 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.215+2309T>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850014 | |||||||
| chr11:45850015 | T | G | 1 | a0001c0001t0003g0181 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.215+2310T>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850015 | |||||||
| chr11:45850016 | T | G | 1 | a0001c0001t0010g0016 | 3 | HG03130.hp2 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.215+2311T>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850016 | |||||||
| chr11:45850112 | G | A | 2 | a0001c0001t0018g0059 a0001c0001t0018g0060 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.215+2407G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850112 | |||||||
| chr11:45850304 | G | A | 1 | a0001c0001t0007g0017 | 3 | HG02622.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.215+2599G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850304 | |||||||
| chr11:45850310 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(49): Show |
96 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.215+2605G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850310 | |||||||
| chr11:45850530 | A | G | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.215+2825A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850530 | |||||||
| chr11:45850642 | G | GT | 12 | a0001c0001t0001g0169 a0001c0001t0003g0011 a0001c0001t0003g0040 others(9): Show |
18 | HG00099.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.215+2938dupT | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 45850642 | ||||||
| chr11:45850827 | C | T | 7 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0063 others(4): Show |
9 | HG02602.hp2 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+3122C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850827 | |||||||
| chr11:45850830 | C | CTACA | 7 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0063 others(4): Show |
9 | HG02602.hp2 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.215+3126_215+3129d others(6): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 45850830 | ||||||
| chr11:45850929 | G | T | 2 | a0001c0001t0004g0031 a0001c0001t0004g0089 |
3 | NA18992.hp1 NA19056.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.215+3224G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850929 | |||||||
| chr11:45850937 | C | G | 1 | a0001c0001t0029g0126 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.215+3232C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45850937 | |||||||
| chr11:45851029 | CT | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(94): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.215+3339delT | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 45851029 | ||||||
| chr11:45851288 | G | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0211 a0001c0001t0001g0212 others(1): Show |
5 | HG01934.hp1 HG03688.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+3583G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45851288 | |||||||
| chr11:45851428 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.215+3723C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45851428 | |||||||
| chr11:45851452 | A | G | 2 | a0001c0001t0004g0030 a0001c0001t0004g0087 |
3 | HG00741.hp2 HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.215+3747A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45851452 | |||||||
| chr11:45851540 | A | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
93 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.215+3835A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45851540 | |||||||
| chr11:45851897 | A | G | 32 | a0001c0001t0001g0169 a0001c0001t0003g0011 a0001c0001t0003g0018 others(29): Show |
48 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.216-4085A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45851897 | |||||||
| chr11:45852713 | A | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.216-3269A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45852713 | |||||||
| chr11:45852853 | T | G | 2 | a0001c0001t0008g0012 a0001c0001t0008g0214 |
5 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.216-3129T>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45852853 | |||||||
| chr11:45853048 | G | T | 1 | a0001c0001t0003g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.216-2934G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45853048 | |||||||
| chr11:45853154 | A | G | 6 | a0001c0001t0006g0010 a0001c0001t0006g0015 a0001c0001t0006g0105 others(3): Show |
11 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.216-2828A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45853154 | |||||||
| chr11:45853429 | T | C | 32 | a0001c0001t0001g0169 a0001c0001t0003g0011 a0001c0001t0003g0018 others(29): Show |
48 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.216-2553T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45853429 | |||||||
| chr11:45853610 | A | G | 1 | a0001c0001t0004g0086 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.216-2372A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45853610 | |||||||
| chr11:45853645 | AC | A | 32 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(29): Show |
49 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.216-2334delC | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 45853645 | ||||||
| chr11:45853806 | C | T | 1 | a0001c0001t0004g0085 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.216-2176C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45853806 | |||||||
| chr11:45853841 | A | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(89): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.216-2141A>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45853841 | |||||||
| chr11:45853861 | A | G | 5 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(2): Show |
5 | HG01261.hp1 HG01496.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.216-2121A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45853861 | |||||||
| chr11:45853977 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.216-2005G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45853977 | |||||||
| chr11:45853987 | C | T | 3 | a0001c0001t0005g0004 a0001c0001t0005g0061 a0001c0001t0005g0062 |
12 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.216-1995C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45853987 | |||||||
| chr11:45854025 | G | T | 1 | a0001c0001t0008g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.216-1957G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854025 | |||||||
| chr11:45854066 | G | A | 2 | a0001c0001t0009g0063 a0001c0001t0009g0064 |
2 | HG02602.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.216-1916G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854066 | |||||||
| chr11:45854288 | C | T | 1 | a0001c0001t0010g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.216-1694C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854288 | |||||||
| chr11:45854367 | G | A | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216-1615G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854367 | |||||||
| chr11:45854370 | G | A | 1 | a0001c0001t0002g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.216-1612G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854370 | |||||||
| chr11:45854372 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.216-1610G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854372 | |||||||
| chr11:45854375 | A | G | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216-1607A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854375 | |||||||
| chr11:45854383 | T | A | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216-1599T>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854383 | |||||||
| chr11:45854404 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(89): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.216-1578A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854404 | |||||||
| chr11:45854458 | C | T | 2 | a0001c0001t0018g0059 a0001c0001t0018g0060 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.216-1524C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854458 | |||||||
| chr11:45854643 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(167): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.216-1339T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45854643 | |||||||
| chr11:45855065 | C | T | 6 | a0001c0001t0006g0010 a0001c0001t0006g0015 a0001c0001t0006g0105 others(3): Show |
11 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.216-917C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855065 | |||||||
| chr11:45855070 | A | T | 2 | a0001c0001t0004g0029 a0001c0001t0004g0090 |
3 | NA18983.hp2 NA18998.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.216-912A>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855070 | |||||||
| chr11:45855169 | C | G | 7 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0063 others(4): Show |
9 | HG02602.hp2 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.216-813C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855169 | |||||||
| chr11:45855211 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.216-771G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855211 | |||||||
| chr11:45855272 | G | C | 2 | a0001c0001t0004g0074 a0001c0001t0004g0075 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.216-710G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855272 | |||||||
| chr11:45855410 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.216-572G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855410 | |||||||
| chr11:45855492 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(167): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.216-490C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855492 | |||||||
| chr11:45855587 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.216-395C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855587 | |||||||
| chr11:45855721 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.216-261T>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855721 | |||||||
| chr11:45855725 | G | A | 1 | a0001c0001t0004g0091 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.216-257G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855725 | |||||||
| chr11:45855727 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.216-255C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855727 | |||||||
| chr11:45855978 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(167): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
splice_region_variant&intron_variant | LOW | c.216-4A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 1/11 | chr11 | 45855978 | |||||||
| chr11:45856137 | C | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(89): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.324+47C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856137 | |||||||
| chr11:45856161 | A | G | 3 | a0001c0001t0005g0004 a0001c0001t0005g0061 a0001c0001t0005g0062 |
12 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+71A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856161 | |||||||
| chr11:45856186 | A | G | 1 | a0001c0001t0003g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.324+96A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856186 | |||||||
| chr11:45856238 | G | C | 1 | a0001c0001t0003g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.324+148G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856238 | |||||||
| chr11:45856439 | A | AG | 92 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(89): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.324+351dupG | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 45856439 | ||||||
| chr11:45856444 | G | T | 8 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(5): Show |
8 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+354G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856444 | |||||||
| chr11:45856519 | G | C | 32 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(29): Show |
49 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.324+429G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856519 | |||||||
| chr11:45856544 | C | T | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.324+454C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856544 | |||||||
| chr11:45856572 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
93 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.324+482G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856572 | |||||||
| chr11:45856669 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(129): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.324+579A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856669 | |||||||
| chr11:45856711 | G | A | 1 | a0001c0001t0007g0017 | 3 | HG02622.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.324+621G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856711 | |||||||
| chr11:45856739 | T | C | 1 | a0001c0001t0016g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.324+649T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856739 | |||||||
| chr11:45856795 | CA | C | 6 | a0001c0001t0001g0207 a0001c0001t0002g0067 a0001c0001t0002g0125 others(3): Show |
6 | HG00639.hp1 HG01168.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+722delA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 45856795 | ||||||
| chr11:45856910 | G | A | 6 | a0001c0001t0006g0010 a0001c0001t0006g0015 a0001c0001t0006g0105 others(3): Show |
11 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+820G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856910 | |||||||
| chr11:45856948 | A | G | 1 | a0001c0001t0004g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.324+858A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856948 | |||||||
| chr11:45856985 | G | T | 20 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(17): Show |
31 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.324+895G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45856985 | |||||||
| chr11:45857027 | C | A | 1 | a0001c0004t0002g0110 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.324+937C>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857027 | |||||||
| chr11:45857040 | A | G | 3 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0053 |
3 | HG01261.hp1 HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.324+950A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857040 | |||||||
| chr11:45857042 | G | A | 6 | a0001c0001t0006g0010 a0001c0001t0006g0015 a0001c0001t0006g0105 others(3): Show |
11 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+952G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857042 | |||||||
| chr11:45857164 | A | C | 1 | a0001c0001t0002g0124 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.324+1074A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857164 | |||||||
| chr11:45857210 | A | G | 1 | a0001c0001t0017g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.324+1120A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857210 | |||||||
| chr11:45857234 | C | T | 1 | a0001c0002t0002g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.324+1144C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857234 | |||||||
| chr11:45857325 | G | C | 26 | a0001c0001t0001g0169 a0001c0001t0003g0011 a0001c0001t0003g0018 others(23): Show |
39 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.324+1235G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857325 | |||||||
| chr11:45857441 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
93 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.325-1290A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857441 | |||||||
| chr11:45857455 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
93 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.325-1276C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857455 | |||||||
| chr11:45857493 | A | G | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.325-1238A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857493 | |||||||
| chr11:45857585 | G | T | 1 | a0001c0001t0003g0164 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.325-1146G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857585 | |||||||
| chr11:45857774 | T | C | 1 | a0001c0001t0005g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.325-957T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45857774 | |||||||
| chr11:45858047 | C | A | 2 | a0001c0001t0018g0059 a0001c0001t0018g0060 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.325-684C>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45858047 | |||||||
| chr11:45858188 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(46): Show |
93 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.325-543T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45858188 | |||||||
| chr11:45858436 | G | A | 1 | a0001c0001t0004g0076 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.325-295G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45858436 | |||||||
| chr11:45858531 | G | A | 1 | a0001c0001t0007g0017 | 3 | HG02622.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.325-200G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45858531 | |||||||
| chr11:45858559 | C | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.325-172C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45858559 | |||||||
| chr11:45858657 | G | A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0111 a0001c0001t0002g0112 |
4 | HG00438.hp2 HG00558.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-74G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 2/11 | chr11 | 45858657 | |||||||
| chr11:45858940 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.467+67C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45858940 | |||||||
| chr11:45858941 | G | A | 8 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(5): Show |
8 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.467+68G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45858941 | |||||||
| chr11:45859030 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467+157C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859030 | |||||||
| chr11:45859216 | G | A | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.467+343G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859216 | |||||||
| chr11:45859330 | T | TTGAGAGG others(6): Show |
93 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(90): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.467+464_467+465ins others(13): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 45859330 | ||||||
| chr11:45859355 | G | A | 3 | a0001c0001t0002g0036 a0001c0001t0002g0132 a0001c0001t0027g0036 |
3 | HG03139.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.467+482G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859355 | |||||||
| chr11:45859391 | G | A | 7 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0063 others(4): Show |
9 | HG02602.hp2 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.467+518G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859391 | |||||||
| chr11:45859428 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.467+555G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859428 | |||||||
| chr11:45859478 | C | T | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.467+605C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859478 | |||||||
| chr11:45859545 | GA | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.467+673delA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859545 | |||||||
| chr11:45859561 | C | CA | 32 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(29): Show |
48 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.467+704dupA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 45859561 | ||||||
| chr11:45859833 | C | T | 1 | a0001c0001t0003g0053 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.467+960C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859833 | |||||||
| chr11:45859846 | AG | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0145 |
4 | HG00280.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.467+974delG | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859846 | |||||||
| chr11:45859869 | G | T | 8 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(5): Show |
8 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.468-979G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859869 | |||||||
| chr11:45859998 | G | A | 6 | a0001c0001t0006g0010 a0001c0001t0006g0015 a0001c0001t0006g0105 others(3): Show |
11 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.468-850G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45859998 | |||||||
| chr11:45860002 | G | T | 1 | a0001c0001t0001g0047 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.468-846G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45860002 | |||||||
| chr11:45860241 | G | A | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.468-607G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45860241 | |||||||
| chr11:45860255 | G | C | 2 | a0001c0001t0018g0059 a0001c0001t0018g0060 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.468-593G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45860255 | |||||||
| chr11:45860386 | T | TA | 70 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(67): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.468-442dupA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 45860386 | ||||||
| chr11:45860386 | T | TAA | 31 | a0001c0001t0001g0169 a0001c0001t0001g0186 a0001c0001t0001g0211 others(28): Show |
46 | HG00099.hp2 HG00609.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.468-443_468-442dup others(2): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 45860386 | ||||||
| chr11:45860386 | TA | T | 21 | a0001c0001t0002g0122 a0001c0001t0004g0083 a0001c0001t0006g0010 others(18): Show |
35 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.468-442delA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 45860386 | ||||||
| chr11:45860707 | T | C | 4 | a0001c0001t0006g0010 a0001c0001t0006g0105 a0001c0001t0006g0143 others(1): Show |
7 | HG00323.hp2 HG01069.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.468-141T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45860707 | |||||||
| chr11:45860783 | G | A | 3 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0053 |
3 | HG01261.hp1 HG01496.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.468-65G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45860783 | |||||||
| chr11:45860784 | G | C | 1 | a0001c0001t0007g0017 | 3 | HG02622.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.468-64G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45860784 | |||||||
| chr11:45860813 | T | C | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.468-35T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 3/11 | chr11 | 45860813 | |||||||
| chr11:45861599 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.653-461G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 4/11 | chr11 | 45861599 | |||||||
| chr11:45861717 | C | G | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.653-343C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 4/11 | chr11 | 45861717 | |||||||
| chr11:45861722 | G | T | 1 | a0001c0001t0007g0017 | 3 | HG02622.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.653-338G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 4/11 | chr11 | 45861722 | |||||||
| chr11:45861747 | T | A | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.653-313T>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 4/11 | chr11 | 45861747 | |||||||
| chr11:45861919 | A | C | 7 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0063 others(4): Show |
9 | HG02602.hp2 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.653-141A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 4/11 | chr11 | 45861919 | |||||||
| chr11:45861999 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.653-61C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 4/11 | chr11 | 45861999 | |||||||
| chr11:45862005 | G | A | 1 | a0001c0001t0022g0176 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.653-55G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 4/11 | chr11 | 45862005 | |||||||
| chr11:45862023 | T | G | 1 | a0001c0001t0004g0097 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.653-37T>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 4/11 | chr11 | 45862023 | |||||||
| chr11:45862229 | AG | A | 3 | a0001c0001t0008g0012 a0001c0001t0008g0182 a0001c0001t0008g0214 |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+82delG | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45862229 | |||||||
| chr11:45862338 | G | T | 1 | a0001c0001t0005g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.741+190G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45862338 | |||||||
| chr11:45862404 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(165): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.741+256T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45862404 | |||||||
| chr11:45862406 | G | GC | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.741+260dupC | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 45862406 | ||||||
| chr11:45862518 | C | T | 1 | a0001c0001t0002g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.741+370C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45862518 | |||||||
| chr11:45862752 | G | A | 3 | a0001c0001t0007g0007 a0001c0001t0007g0146 a0001c0001t0007g0151 |
8 | HG01884.hp1 HG02922.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.741+604G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45862752 | |||||||
| chr11:45862845 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.741+697C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45862845 | |||||||
| chr11:45863201 | G | A | 3 | a0001c0001t0008g0012 a0001c0001t0008g0182 a0001c0001t0008g0214 |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+1053G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45863201 | |||||||
| chr11:45863245 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.741+1097G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45863245 | |||||||
| chr11:45863274 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.741+1126A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45863274 | |||||||
| chr11:45863383 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.741+1235G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45863383 | |||||||
| chr11:45863549 | G | C | 3 | a0001c0001t0008g0012 a0001c0001t0008g0182 a0001c0001t0008g0214 |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+1401G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45863549 | |||||||
| chr11:45863746 | T | C | 1 | a0001c0001t0002g0122 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.741+1598T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45863746 | |||||||
| chr11:45864476 | C | T | 2 | a0001c0001t0018g0059 a0001c0001t0018g0060 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.741+2328C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45864476 | |||||||
| chr11:45864665 | C | T | 1 | a0001c0001t0002g0035 | 2 | NA18963.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.741+2517C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45864665 | |||||||
| chr11:45864821 | T | C | 14 | a0001c0001t0001g0213 a0001c0001t0002g0003 a0001c0001t0002g0033 others(11): Show |
25 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.741+2673T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45864821 | |||||||
| chr11:45864958 | C | T | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.742-2654C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45864958 | |||||||
| chr11:45865121 | T | TA | 10 | a0001c0001t0002g0113 a0001c0001t0003g0050 a0001c0001t0003g0051 others(7): Show |
10 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.742-2479dupA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 45865121 | ||||||
| chr11:45865364 | G | A | 8 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(5): Show |
8 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.742-2248G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45865364 | |||||||
| chr11:45865398 | CAT | C | 6 | a0001c0001t0003g0050 a0001c0001t0003g0054 a0001c0001t0005g0004 others(3): Show |
15 | HG02559.hp2 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.742-2213_742-2212d others(4): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45865398 | |||||||
| chr11:45865949 | G | A | 5 | a0001c0001t0003g0021 a0001c0001t0003g0039 a0001c0001t0003g0156 others(2): Show |
8 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.742-1663G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45865949 | |||||||
| chr11:45865952 | G | C | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.742-1660G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45865952 | |||||||
| chr11:45866012 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.742-1600G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45866012 | |||||||
| chr11:45866410 | A | C | 3 | a0001c0001t0003g0039 a0001c0001t0003g0156 a0001c0001t0003g0166 |
4 | HG02258.hp1 HG02717.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.742-1202A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45866410 | |||||||
| chr11:45866421 | G | A | 8 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(5): Show |
8 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.742-1191G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45866421 | |||||||
| chr11:45866647 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.742-965G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45866647 | |||||||
| chr11:45866655 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0002g0112 |
2 | HG00558.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.742-957A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45866655 | |||||||
| chr11:45866904 | G | A | 1 | a0001c0001t0004g0092 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.742-708G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45866904 | |||||||
| chr11:45867030 | A | G | 1 | a0001c0001t0007g0017 | 3 | HG02622.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.742-582A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45867030 | |||||||
| chr11:45867106 | T | C | 3 | a0001c0001t0011g0037 a0001c0001t0011g0104 a0001c0001t0011g0133 |
4 | HG00140.hp1 HG02698.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.742-506T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45867106 | |||||||
| chr11:45867571 | A | T | 3 | a0001c0001t0011g0037 a0001c0001t0011g0104 a0001c0001t0011g0133 |
4 | HG00140.hp1 HG02698.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.742-41A>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 5/11 | chr11 | 45867571 | |||||||
| chr11:45868069 | C | T | 1 | a0001c0001t0004g0076 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.882+317C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868069 | |||||||
| chr11:45868207 | G | A | 5 | a0001c0001t0002g0034 a0001c0001t0002g0101 a0001c0001t0019g0034 others(2): Show |
5 | NA18967.hp2 NA18973.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+455G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868207 | |||||||
| chr11:45868224 | C | T | 30 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0009 others(27): Show |
47 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.882+472C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868224 | |||||||
| chr11:45868452 | A | G | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.882+700A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868452 | |||||||
| chr11:45868462 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(2): Show |
7 | HG02145.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+710C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868462 | |||||||
| chr11:45868464 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(2): Show |
7 | HG02145.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+712C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868464 | |||||||
| chr11:45868558 | A | G | 7 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0063 others(4): Show |
9 | HG02602.hp2 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+806A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868558 | |||||||
| chr11:45868598 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.882+846C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868598 | |||||||
| chr11:45868599 | G | A | 1 | a0001c0001t0009g0025 | 2 | HG03669.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.882+847G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868599 | |||||||
| chr11:45868687 | A | C | 1 | a0001c0001t0002g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.883-819A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868687 | |||||||
| chr11:45868905 | G | C | 3 | a0001c0001t0008g0012 a0001c0001t0008g0182 a0001c0001t0008g0214 |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-601G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45868905 | |||||||
| chr11:45869157 | C | T | 1 | a0001c0001t0008g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.883-349C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45869157 | |||||||
| chr11:45869255 | G | A | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-251G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45869255 | |||||||
| chr11:45869441 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.883-65C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 6/11 | chr11 | 45869441 | |||||||
| chr11:45869866 | C | T | 1 | a0001c0001t0029g0126 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1194+49C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 7/11 | chr11 | 45869866 | |||||||
| chr11:45869867 | G | A | 40 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(37): Show |
62 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1194+50G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 7/11 | chr11 | 45869867 | |||||||
| chr11:45869918 | C | G | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1194+101C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 7/11 | chr11 | 45869918 | |||||||
| chr11:45869957 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(164): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1195-96A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 7/11 | chr11 | 45869957 | |||||||
| chr11:45870037 | C | T | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1195-16C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 7/11 | chr11 | 45870037 | |||||||
| chr11:45870292 | G | A | 1 | a0001c0001t0008g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1347-38G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 8/11 | chr11 | 45870292 | |||||||
| chr11:45870657 | G | A | 1 | a0001c0001t0006g0147 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1549+125G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 9/11 | chr11 | 45870657 | |||||||
| chr11:45870724 | G | A | 3 | a0001c0001t0005g0004 a0001c0001t0005g0061 a0001c0001t0005g0062 |
12 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1550-118G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 9/11 | chr11 | 45870724 | |||||||
| chr11:45871048 | G | A | 1 | a0001c0001t0016g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1642+114G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871048 | |||||||
| chr11:45871104 | G | A | 1 | a0001c0001t0009g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1642+170G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871104 | |||||||
| chr11:45871158 | CT | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(2): Show |
7 | HG02145.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1642+225delT | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871158 | |||||||
| chr11:45871213 | C | T | 12 | a0001c0001t0005g0004 a0001c0001t0005g0061 a0001c0001t0005g0062 others(9): Show |
23 | HG02559.hp1 HG02559.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.1642+279C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871213 | |||||||
| chr11:45871292 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1642+358A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871292 | |||||||
| chr11:45871302 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1642+368G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871302 | |||||||
| chr11:45871476 | G | A | 1 | a0001c0001t0007g0151 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1642+542G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871476 | |||||||
| chr11:45871498 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1642+564A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871498 | |||||||
| chr11:45871502 | G | C | 1 | a0001c0001t0008g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1642+568G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871502 | |||||||
| chr11:45871517 | G | C | 2 | a0001c0001t0004g0031 a0001c0001t0004g0089 |
3 | NA18992.hp1 NA19056.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1643-575G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871517 | |||||||
| chr11:45871621 | T | C | 17 | a0001c0001t0006g0010 a0001c0001t0006g0015 a0001c0001t0006g0105 others(14): Show |
31 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1643-471T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871621 | |||||||
| chr11:45871683 | G | A | 1 | a0001c0001t0003g0208 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1643-409G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45871683 | |||||||
| chr11:45872079 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1643-13C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 10/11 | chr11 | 45872079 | |||||||
| chr11:45872275 | G | C | 2 | a0001c0001t0003g0158 a0001c0001t0003g0174 |
2 | HG02074.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.*2+42G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872275 | |||||||
| chr11:45872280 | T | G | 1 | a0001c0001t0004g0097 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.*2+47T>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872280 | |||||||
| chr11:45872281 | G | C | 1 | a0001c0001t0003g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*2+48G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872281 | |||||||
| chr11:45872345 | G | T | 1 | a0001c0001t0025g0172 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.*2+112G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872345 | |||||||
| chr11:45872351 | C | G | 2 | a0001c0001t0015g0072 a0001c0001t0015g0082 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.*2+118C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872351 | |||||||
| chr11:45872563 | T | C | 3 | a0001c0001t0002g0013 a0001c0001t0002g0067 a0001c0001t0002g0068 |
5 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.*2+330T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872563 | |||||||
| chr11:45872586 | C | CATA | 5 | a0001c0001t0001g0022 a0001c0001t0012g0022 a0001c0001t0012g0185 others(2): Show |
6 | HG02148.hp2 HG02293.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.*2+374_*2+376dupAA others(1): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45872586 | ||||||
| chr11:45872691 | C | A | 1 | a0001c0001t0004g0097 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.*2+458C>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872691 | |||||||
| chr11:45872712 | C | A | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*2+479C>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872712 | |||||||
| chr11:45872749 | C | G | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.*2+516C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872749 | |||||||
| chr11:45872804 | G | A | 3 | a0001c0001t0005g0004 a0001c0001t0005g0061 a0001c0001t0005g0062 |
12 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.*2+571G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45872804 | |||||||
| chr11:45873085 | C | G | 39 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(36): Show |
58 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.*2+852C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45873085 | |||||||
| chr11:45873388 | A | G | 1 | a0001c0001t0003g0161 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.*2+1155A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45873388 | |||||||
| chr11:45873541 | G | A | 1 | a0001c0001t0009g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.*2+1308G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45873541 | |||||||
| chr11:45873611 | A | G | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*2+1378A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45873611 | |||||||
| chr11:45873781 | G | T | 1 | a0001c0001t0004g0081 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.*2+1548G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45873781 | |||||||
| chr11:45873830 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.*2+1597G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45873830 | |||||||
| chr11:45874234 | C | T | 1 | a0001c0001t0004g0096 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.*2+2001C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45874234 | |||||||
| chr11:45874262 | A | T | 1 | a0001c0001t0026g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.*2+2029A>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45874262 | |||||||
| chr11:45874333 | T | A | 1 | a0001c0002t0002g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.*2+2100T>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45874333 | |||||||
| chr11:45874604 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.*2+2371G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45874604 | |||||||
| chr11:45874835 | T | C | 8 | a0001c0001t0004g0006 a0001c0001t0004g0029 a0001c0001t0004g0031 others(5): Show |
15 | HG02129.hp1 NA18939.hp2 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.*2+2602T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45874835 | |||||||
| chr11:45874870 | G | T | 1 | a0001c0001t0002g0107 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.*2+2637G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45874870 | |||||||
| chr11:45875246 | T | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(44): Show |
91 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.*2+3013T>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45875246 | |||||||
| chr11:45875321 | G | A | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.*2+3088G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45875321 | |||||||
| chr11:45875399 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.*2+3166T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45875399 | |||||||
| chr11:45875471 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.*2+3238G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45875471 | |||||||
| chr11:45875516 | G | A | 1 | a0001c0001t0010g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.*2+3283G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45875516 | |||||||
| chr11:45875526 | A | G | 45 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(42): Show |
67 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.*2+3293A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45875526 | |||||||
| chr11:45875811 | G | GCATCCTC others(10): Show |
1 | a0001c0001t0004g0097 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.*2+3579_*2+3595dup others(17): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45875811 | ||||||
| chr11:45875904 | G | A | 3 | a0001c0001t0002g0035 a0001c0001t0002g0102 a0001c0001t0002g0116 |
4 | NA18963.hp1 NA18979.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.*2+3671G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45875904 | |||||||
| chr11:45875918 | A | G | 4 | a0001c0001t0003g0019 a0001c0001t0003g0154 a0001c0001t0003g0160 others(1): Show |
6 | HG00609.hp1 HG02129.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.*2+3685A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45875918 | |||||||
| chr11:45875938 | G | T | 1 | a0001c0001t0003g0052 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*2+3705G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45875938 | |||||||
| chr11:45876094 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0001g0198 a0001c0001t0001g0203 others(1): Show |
4 | HG01258.hp2 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.*2+3861C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45876094 | |||||||
| chr11:45876100 | A | C | 82 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(79): Show |
129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.*2+3867A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45876100 | |||||||
| chr11:45876157 | G | A | 3 | a0001c0001t0005g0004 a0001c0001t0005g0061 a0001c0001t0005g0062 |
12 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.*2+3924G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45876157 | |||||||
| chr11:45876226 | C | CTCTGA | 2 | a0001c0001t0008g0012 a0001c0001t0008g0214 |
5 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.*2+3994_*2+3998dup others(5): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45876226 | ||||||
| chr11:45876749 | A | T | 1 | a0001c0001t0001g0023 | 3 | NA19077.hp1 NA19082.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.*3-4165A>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45876749 | |||||||
| chr11:45876801 | G | C | 1 | a0001c0001t0012g0190 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.*3-4113G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45876801 | |||||||
| chr11:45876921 | A | T | 1 | a0001c0001t0008g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.*3-3993A>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45876921 | |||||||
| chr11:45877190 | G | C | 3 | a0001c0001t0011g0037 a0001c0001t0011g0104 a0001c0001t0011g0133 |
4 | HG00140.hp1 HG02698.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3-3724G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45877190 | |||||||
| chr11:45877209 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*3-3705C>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45877209 | |||||||
| chr11:45877333 | C | T | 2 | a0001c0001t0003g0020 a0001c0001t0003g0163 |
4 | HG01109.hp2 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3-3581C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45877333 | |||||||
| chr11:45877368 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0202 |
3 | NA18943.hp2 NA18986.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.*3-3546A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45877368 | |||||||
| chr11:45877880 | A | G | 1 | a0001c0001t0003g0171 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.*3-3034A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45877880 | |||||||
| chr11:45877884 | G | A | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*3-3030G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45877884 | |||||||
| chr11:45878077 | C | G | 1 | a0001c0001t0002g0119 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.*3-2837C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878077 | |||||||
| chr11:45878240 | A | C | 43 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(40): Show |
65 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.*3-2674A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878240 | |||||||
| chr11:45878328 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.*3-2586C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878328 | |||||||
| chr11:45878331 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*3-2583C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878331 | |||||||
| chr11:45878361 | A | C | 1 | a0001c0001t0018g0060 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.*3-2553A>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878361 | |||||||
| chr11:45878411 | A | G | 32 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0019 others(29): Show |
48 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.*3-2503A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878411 | |||||||
| chr11:45878461 | A | G | 2 | a0001c0001t0017g0098 a0001c0001t0017g0099 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.*3-2453A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878461 | |||||||
| chr11:45878811 | TGGGAGGC others(1): Show |
T | 3 | a0001c0001t0011g0037 a0001c0001t0011g0104 a0001c0001t0011g0133 |
4 | HG00140.hp1 HG02698.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3-2102_*3-2095del others(8): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878811 | |||||||
| chr11:45878849 | G | C | 1 | a0001c0001t0026g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.*3-2065G>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878849 | |||||||
| chr11:45878920 | T | TA | 44 | a0001c0001t0001g0044 a0001c0001t0001g0180 a0001c0001t0001g0186 others(41): Show |
61 | HG00099.hp2 HG00609.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.*3-1966dupA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45878920 | ||||||
| chr11:45878920 | T | TAA | 9 | a0001c0001t0001g0193 a0001c0001t0002g0117 a0001c0001t0003g0040 others(6): Show |
10 | HG00738.hp1 HG01243.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.*3-1967_*3-1966dup others(2): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45878920 | ||||||
| chr11:45878920 | TA | T | 13 | a0001c0001t0001g0045 a0001c0001t0001g0187 a0001c0001t0002g0108 others(10): Show |
24 | HG01074.hp2 HG01192.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.*3-1966delA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45878920 | ||||||
| chr11:45878920 | TAA | T | 7 | a0001c0001t0008g0130 a0001c0001t0009g0025 a0001c0001t0009g0063 others(4): Show |
8 | HG02602.hp2 HG03017.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.*3-1967_*3-1966del others(2): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45878920 | ||||||
| chr11:45878920 | TAAA | T | 16 | a0001c0001t0004g0085 a0001c0001t0004g0086 a0001c0001t0004g0094 others(13): Show |
25 | HG00280.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.*3-1968_*3-1966del others(3): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45878920 | ||||||
| chr11:45878920 | TAAAA | T | 32 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(29): Show |
56 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.*3-1969_*3-1966del others(4): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45878920 | ||||||
| chr11:45878920 | TAAAAA | T | 6 | a0001c0001t0004g0075 a0001c0001t0004g0087 a0001c0001t0004g0095 others(3): Show |
6 | HG00323.hp1 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.*3-1970_*3-1966del others(5): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45878920 | ||||||
| chr11:45878920 | TAAAAAAA others(7): Show |
T | 3 | a0001c0001t0008g0012 a0001c0001t0008g0182 a0001c0001t0008g0214 |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.*3-1979_*3-1966del others(14): Show |
CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45878920 | ||||||
| chr11:45878951 | C | T | 1 | a0001c0001t0004g0078 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.*3-1963C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45878951 | |||||||
| chr11:45879039 | G | A | 1 | a0001c0001t0006g0147 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*3-1875G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45879039 | |||||||
| chr11:45879229 | C | CA | 10 | a0001c0001t0001g0069 a0001c0001t0001g0194 a0001c0001t0003g0159 others(7): Show |
12 | HG00544.hp2 HG02071.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.*3-1672dupA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45879229 | ||||||
| chr11:45879229 | CA | C | 5 | a0001c0001t0001g0070 a0001c0001t0011g0037 a0001c0001t0011g0104 others(2): Show |
6 | HG00140.hp1 HG02698.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.*3-1672delA | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr11 | 45879229 | ||||||
| chr11:45879257 | G | A | 3 | a0001c0001t0002g0036 a0001c0001t0002g0132 a0001c0001t0027g0036 |
3 | HG03139.hp1 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*3-1657G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45879257 | |||||||
| chr11:45879540 | T | A | 37 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(34): Show |
56 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.*3-1374T>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45879540 | |||||||
| chr11:45879558 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.*3-1356C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45879558 | |||||||
| chr11:45879594 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.*3-1320G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45879594 | |||||||
| chr11:45879597 | T | C | 8 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(5): Show |
8 | HG01243.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.*3-1317T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45879597 | |||||||
| chr11:45879859 | A | G | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*3-1055A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45879859 | |||||||
| chr11:45879946 | T | C | 7 | a0001c0001t0003g0011 a0001c0001t0003g0040 a0001c0001t0003g0042 others(4): Show |
12 | HG00099.hp2 HG00733.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.*3-968T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45879946 | |||||||
| chr11:45879975 | A | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0207 |
2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.*3-939A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45879975 | |||||||
| chr11:45880024 | A | T | 1 | a0001c0001t0026g0139 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.*3-890A>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45880024 | |||||||
| chr11:45880064 | G | T | 3 | a0001c0001t0011g0037 a0001c0001t0011g0104 a0001c0001t0011g0133 |
4 | HG00140.hp1 HG02698.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3-850G>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45880064 | |||||||
| chr11:45880158 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3-756T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45880158 | |||||||
| chr11:45880177 | C | G | 1 | a0001c0001t0002g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.*3-737C>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45880177 | |||||||
| chr11:45880427 | T | G | 1 | a0001c0001t0005g0062 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.*3-487T>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45880427 | |||||||
| chr11:45880442 | A | G | 3 | a0001c0001t0008g0129 a0001c0001t0008g0130 a0001c0001t0008g0131 |
3 | HG02818.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*3-472A>G | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45880442 | |||||||
| chr11:45880661 | C | T | 3 | a0001c0001t0005g0004 a0001c0001t0005g0061 a0001c0001t0005g0062 |
12 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.*3-253C>T | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45880661 | |||||||
| chr11:45880701 | T | C | 1 | a0001c0001t0004g0075 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.*3-213T>C | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45880701 | |||||||
| chr11:45880774 | G | A | 2 | a0001c0001t0002g0136 a0001c0001t0004g0080 |
2 | HG02132.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.*3-140G>A | CRY2 | ENSG00000121671.12 | transcript | ENST00000616080.2 | protein_coding | 11/11 | chr11 | 45880774 |