Item | Value |
---|---|
geneid | 146227 |
ensemblid | ENSG00000166546.15 |
hgncid | 24160 |
symbol | BEAN1 |
name | brain expressed associated with NEDD4 1 |
refseq_nuc | NM_001178020.3 |
refseq_prot | NP_001171491.1 |
ensembl_nuc | ENST00000536005.7 |
ensembl_prot | ENSP00000442793.2 |
mane_status | MANE Select |
chr | chr16 |
start | 66427295 |
end | 66482833 |
strand | + |
ver | v1.2 |
region | chr16:66427295-66482833 |
region5000 | chr16:66422295-66487833 |
regionname0 | BEAN1_chr16_66427295_66482833 |
regionname5000 | BEAN1_chr16_66422295_66487833 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 259 | 291 | 85 | 52 | 110 | 9 | 34 | 76 | BEAN1_chr16_66422295_66487833 | BEAN1 | MSFKR others(254): Show |
chr16 | 66422295 | 66487833 |
a0002 | 0/1 | 259 | 2 | 0 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | MSFKR others(254): Show |
chr16 | 66422295 | 66487833 |
a0003 | 0/0 | 259 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BEAN1_chr16_66422295_66487833 | BEAN1 | MSFKR others(254): Show |
chr16 | 66422295 | 66487833 |
a0004 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | MSFKR others(254): Show |
chr16 | 66422295 | 66487833 |
a0005 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | MSFKR others(254): Show |
chr16 | 66422295 | 66487833 |
a0006 | 0/0 | 259 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | MSFKR others(254): Show |
chr16 | 66422295 | 66487833 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 777 | 289 | 85 | 51 | 109 | 9 | 34 | BEAN1_chr16_66422295_66487833 | BEAN1 | ATGTC others(772): Show |
chr16 | 66422295 | 66487833 | ||
a0001c0005 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | ATGTC others(772): Show |
chr16 | 66422295 | 66487833 | ||
a0001c0007 | 0/0 | 777 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | ATGTC others(772): Show |
chr16 | 66422295 | 66487833 | ||
a0002c0002 | 0/1 | 777 | 2 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | ATGTC others(772): Show |
chr16 | 66422295 | 66487833 | ||
a0003c0003 | 0/0 | 777 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | ATGTC others(772): Show |
chr16 | 66422295 | 66487833 | ||
a0004c0008 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | ATGTC others(772): Show |
chr16 | 66422295 | 66487833 | ||
a0005c0006 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | ATGTC others(772): Show |
chr16 | 66422295 | 66487833 | ||
a0006c0004 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | ATGTC others(772): Show |
chr16 | 66422295 | 66487833 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2907 | 175 | 40 | 35 | 66 | 6 | 27 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0002 | 0/0 | 2907 | 45 | 11 | 5 | 22 | 1 | 6 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0003 | 0/0 | 2907 | 42 | 14 | 8 | 19 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0004 | 0/0 | 2907 | 15 | 13 | 2 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0005 | 0/0 | 2907 | 2 | 0 | 0 | 0 | 2 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0006 | 0/0 | 2907 | 2 | 1 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0007 | 0/0 | 2907 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0008 | 0/0 | 2907 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0009 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0010 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0011 | 0/0 | 2947 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2942): Show |
chr16 | 66422295 | 66487833 |
a0001c0001t0012 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0005t0001 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0001c0007t0003 | 0/0 | 2907 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0002c0002t0001 | 0/1 | 2907 | 2 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0003c0003t0002 | 0/0 | 2907 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0004c0008t0001 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0005c0006t0001 | 0/0 | 2907 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
a0006c0004t0003 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | GCGAC others(2902): Show |
chr16 | 66422295 | 66487833 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0011g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0005t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0001c0007t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0002c0002t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0003c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0004c0008t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0005c0006t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
a0006c0004t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0005 | g0087 | EUR | GBR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0188 | EUR | GBR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | FIN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00609 | hp1 | a0004 | c0008 | t0001 | g0050 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01175 | hp2 | a0001 | c0007 | t0003 | g0245 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01243 | hp1 | a0001 | c0001 | t0011 | g0277 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0231 | EUR | IBS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02071 | hp2 | a0005 | c0006 | t0001 | g0187 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CDX | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CDX | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CDX | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02809 | hp2 | a0001 | c0001 | t0012 | g0105 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0284 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03041 | hp1 | a0006 | c0004 | t0003 | g0197 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18984 | hp1 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19007 | hp1 | a0003 | c0003 | t0002 | g0080 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19011 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19068 | hp1 | a0003 | c0003 | t0002 | g0158 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19082 | hp1 | a0001 | c0005 | t0001 | g0200 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ASW | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ASW | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | GIH | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | USA | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | USA | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | USA | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0089 | REF | REF | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0126 | REF | REF | BEAN1_chr16_66422295_66487833 | BEAN1 | chr16 | 66422295 | 66487833 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66469781 | C | T | 1 | a0004 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.205C>T | p.Arg69Trp | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/5 | 424/2907 | 205/780 | 69/259 | chr16 | 66469781 | |||
chr16:66469802 | C | A | 1 | a0002 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.226C>A | p.Arg76Ser | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/5 | 445/2907 | 226/780 | 76/259 | chr16 | 66469802 | |||
chr16:66477657 | C | A | 1 | a0006 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.387C>A | p.Asp129Glu | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/5 | 606/2907 | 387/780 | 129/259 | chr16 | 66477657 | |||
chr16:66480636 | A | G | 1 | a0005 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.491A>G | p.Asp164Gly | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 710/2907 | 491/780 | 164/259 | chr16 | 66480636 | |||
chr16:66480709 | C | G | 1 | a0003 | 2 | NA19007.hp1 NA19068.hp1 |
missense_variant | MODERATE | c.564C>G | p.His188Gln | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 783/2907 | 564/780 | 188/259 | chr16 | 66480709 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66477657 | C | T | 1 | a0001c0007 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.387C>T | p.Asp129Asp | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/5 | 606/2907 | 387/780 | 129/259 | chr16 | 66477657 | |||
chr16:66480841 | G | A | 1 | a0001c0005 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.696G>A | p.Pro232Pro | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 915/2907 | 696/780 | 232/259 | chr16 | 66480841 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66427314 | G | T | 2 | a0001c0001t0007 a0001c0001t0008 |
4 | HG03209.hp1 HG03453.hp2 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-200G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/5 | 10363 | chr16 | 66427314 | ||||||
chr16:66481059 | C | T | 4 | a0001c0001t0003 a0001c0001t0008 a0001c0007t0003 others(1): Show |
46 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*134C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 134 | chr16 | 66481059 | ||||||
chr16:66481217 | G | A | 2 | a0001c0001t0002 a0003c0003t0002 |
47 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*292G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 292 | chr16 | 66481217 | ||||||
chr16:66481323 | A | G | 1 | a0001c0001t0012 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 398 | chr16 | 66481323 | ||||||
chr16:66481349 | G | T | 1 | a0001c0001t0004 | 15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*424G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 424 | chr16 | 66481349 | ||||||
chr16:66481431 | G | A | 1 | a0001c0001t0009 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 506 | chr16 | 66481431 | ||||||
chr16:66481460 | C | T | 1 | a0001c0001t0006 | 2 | HG02886.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*535C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 535 | chr16 | 66481460 | ||||||
chr16:66481753 | G | A | 1 | a0001c0001t0010 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 828 | chr16 | 66481753 | ||||||
chr16:66482130 | G | A | 1 | a0001c0001t0009 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 1205 | chr16 | 66482130 | ||||||
chr16:66482344 | T | C | 1 | a0001c0001t0005 | 2 | HG00140.hp1 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1419T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 1419 | chr16 | 66482344 | ||||||
chr16:66482666 | G | GGGAAAAA others(33): Show |
1 | a0001c0001t0011 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1742_*1781dupGGAA others(36): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 1782 | INFO_REALIGN_3_PRIME | chr16 | 66482666 | |||||
chr16:66482676 | G | A | 1 | a0001c0001t0012 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1751G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 5/5 | 1751 | chr16 | 66482676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:66427531 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-83+100G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66427531 | |||||||
chr16:66427648 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-83+217G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66427648 | |||||||
chr16:66427694 | G | A | 1 | a0001c0001t0004g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-83+263G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66427694 | |||||||
chr16:66427705 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-83+274T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66427705 | |||||||
chr16:66428024 | G | A | 1 | a0001c0001t0002g0018 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-83+593G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428024 | |||||||
chr16:66428057 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-83+626A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428057 | |||||||
chr16:66428124 | G | T | 2 | a0001c0001t0001g0283 a0001c0001t0006g0284 |
2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-83+693G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428124 | |||||||
chr16:66428210 | C | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-83+779C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428210 | |||||||
chr16:66428311 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-83+880C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66428311 | |||||||
chr16:66429054 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-83+1623C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429054 | |||||||
chr16:66429145 | G | T | 3 | a0001c0001t0002g0279 a0001c0001t0002g0280 a0001c0001t0003g0278 |
3 | HG02129.hp2 NA18963.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-83+1714G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429145 | |||||||
chr16:66429157 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(94): Show |
103 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-83+1726G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429157 | |||||||
chr16:66429232 | C | T | 3 | a0001c0001t0003g0104 a0001c0001t0003g0106 a0001c0001t0012g0105 |
3 | HG01884.hp1 HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-83+1801C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429232 | |||||||
chr16:66429531 | T | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-83+2100T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429531 | |||||||
chr16:66429607 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-83+2176C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66429607 | |||||||
chr16:66429838 | AAC | A | 22 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(19): Show |
23 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-83+2411_-83+2412d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66429838 | ||||||
chr16:66430210 | C | G | 3 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0102 |
5 | HG00738.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-83+2779C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66430210 | |||||||
chr16:66430210 | C | T | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-83+2779C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66430210 | |||||||
chr16:66430776 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(86): Show |
95 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.-83+3345G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66430776 | |||||||
chr16:66430977 | C | A | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(18): Show |
22 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.-83+3546C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66430977 | |||||||
chr16:66431278 | C | T | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-83+3847C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431278 | |||||||
chr16:66431603 | G | GT | 142 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-83+4183dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66431603 | ||||||
chr16:66431603 | GT | G | 22 | a0001c0001t0001g0107 a0001c0001t0001g0110 a0001c0001t0001g0111 others(19): Show |
23 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.-83+4183delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66431603 | ||||||
chr16:66431635 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-83+4204C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431635 | |||||||
chr16:66431660 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-83+4229A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431660 | |||||||
chr16:66431869 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-83+4438C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431869 | |||||||
chr16:66431876 | G | A | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-83+4445G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66431876 | |||||||
chr16:66432459 | C | G | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-83+5028C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432459 | |||||||
chr16:66432570 | C | T | 1 | a0001c0001t0004g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-82-5025C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432570 | |||||||
chr16:66432635 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(195): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-82-4960A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432635 | |||||||
chr16:66432685 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-82-4910C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432685 | |||||||
chr16:66432736 | A | G | 2 | a0001c0001t0001g0283 a0001c0001t0006g0284 |
2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-82-4859A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432736 | |||||||
chr16:66432742 | T | C | 20 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(17): Show |
21 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-82-4853T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432742 | |||||||
chr16:66432791 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-82-4804G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66432791 | |||||||
chr16:66433100 | TTTATTTT others(2): Show |
T | 4 | a0001c0001t0002g0092 a0001c0001t0002g0279 a0001c0001t0002g0280 others(1): Show |
4 | HG02129.hp2 NA18963.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82-4477_-82-4469d others(11): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66433100 | ||||||
chr16:66433366 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-82-4229C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433366 | |||||||
chr16:66433392 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-82-4203G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433392 | |||||||
chr16:66433548 | G | A | 22 | a0001c0001t0001g0015 a0001c0001t0001g0135 a0001c0001t0001g0136 others(19): Show |
23 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.-82-4047G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433548 | |||||||
chr16:66433558 | CCTTCCTA others(9): Show |
C | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-82-4036_-82-4021d others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433558 | |||||||
chr16:66433584 | A | AAGCCAAT | 24 | a0001c0001t0001g0036 a0001c0001t0001g0257 a0001c0001t0001g0258 others(21): Show |
25 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.-82-4010_-82-4009i others(9): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66433584 | ||||||
chr16:66433985 | C | T | 18 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0264 others(15): Show |
19 | HG00642.hp2 HG00741.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-82-3610C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66433985 | |||||||
chr16:66434156 | G | A | 1 | a0001c0001t0003g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-82-3439G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434156 | |||||||
chr16:66434197 | G | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
21 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-82-3398G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434197 | |||||||
chr16:66434206 | CCCCCGAC others(11): Show |
C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-82-3372_-82-3355d others(20): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66434206 | ||||||
chr16:66434219 | C | T | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
17 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-82-3376C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434219 | |||||||
chr16:66434319 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0011g0277 |
2 | HG01243.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-82-3276G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434319 | |||||||
chr16:66434450 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0003g0256 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-82-3145G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434450 | |||||||
chr16:66434609 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(184): Show |
196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.-82-2986T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434609 | |||||||
chr16:66434669 | G | A | 9 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(6): Show |
9 | HG00673.hp1 HG02165.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.-82-2926G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434669 | |||||||
chr16:66434716 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(95): Show |
104 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-82-2879G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434716 | |||||||
chr16:66434785 | T | G | 4 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0008g0006 others(1): Show |
5 | HG02109.hp2 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82-2810T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66434785 | |||||||
chr16:66435040 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01169.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-82-2555G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435040 | |||||||
chr16:66435068 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-82-2527G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435068 | |||||||
chr16:66435241 | G | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(39): Show |
45 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.-82-2354G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435241 | |||||||
chr16:66435372 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-82-2223A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435372 | |||||||
chr16:66435404 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-82-2191T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435404 | |||||||
chr16:66435577 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-82-2018T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435577 | |||||||
chr16:66435651 | A | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(191): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-82-1944A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435651 | |||||||
chr16:66435812 | G | A | 29 | a0001c0001t0001g0034 a0001c0001t0001g0110 a0001c0001t0001g0111 others(26): Show |
30 | HG01109.hp2 HG02109.hp2 HG02451.hp1 others(27): Show |
intron_variant | MODIFIER | c.-82-1783G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435812 | |||||||
chr16:66435897 | T | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG01169.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-82-1698T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66435897 | |||||||
chr16:66436087 | C | G | 24 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0253 others(21): Show |
25 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-82-1508C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436087 | |||||||
chr16:66436266 | C | CT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0032 others(94): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-82-1310dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66436266 | ||||||
chr16:66436330 | T | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.-82-1265T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436330 | |||||||
chr16:66436443 | A | AT | 28 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0130 others(25): Show |
29 | HG00544.hp1 HG00642.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.-82-1136dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66436443 | ||||||
chr16:66436513 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0130 |
2 | HG03927.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-82-1082T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436513 | |||||||
chr16:66436558 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-82-1037G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436558 | |||||||
chr16:66436559 | T | G | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-82-1036T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436559 | |||||||
chr16:66436580 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0002g0213 |
2 | NA18612.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-82-1015T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436580 | |||||||
chr16:66436829 | T | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0157 a0001c0001t0002g0044 others(2): Show |
5 | NA18953.hp1 NA19003.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-82-766T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436829 | |||||||
chr16:66436919 | A | G | 23 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0253 others(20): Show |
24 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-82-676A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66436919 | |||||||
chr16:66437104 | G | GTAA | 14 | a0001c0001t0001g0034 a0001c0001t0001g0110 a0001c0001t0001g0111 others(11): Show |
14 | HG01109.hp2 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-82-470_-82-468dup others(3): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66437104 | ||||||
chr16:66437270 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0037 others(68): Show |
74 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-82-325G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437270 | |||||||
chr16:66437280 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.-82-315G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437280 | |||||||
chr16:66437314 | T | C | 1 | a0001c0001t0003g0160 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-82-281T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437314 | |||||||
chr16:66437328 | C | CCACT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(191): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.-82-265_-82-264ins others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr16 | 66437328 | ||||||
chr16:66437371 | C | T | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-82-224C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437371 | |||||||
chr16:66437544 | C | A | 75 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0034 others(72): Show |
80 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-82-51C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 1/4 | chr16 | 66437544 | |||||||
chr16:66437857 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0003g0137 others(2): Show |
5 | HG00733.hp1 HG01099.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+156G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66437857 | |||||||
chr16:66438067 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0283 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+366G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438067 | |||||||
chr16:66438106 | C | T | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+405C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438106 | |||||||
chr16:66438149 | C | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+448C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438149 | |||||||
chr16:66438213 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.25+512G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438213 | |||||||
chr16:66438239 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+538C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438239 | |||||||
chr16:66438257 | G | A | 2 | a0001c0001t0003g0124 a0001c0001t0009g0019 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.25+556G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438257 | |||||||
chr16:66438257 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.25+556G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438257 | |||||||
chr16:66438263 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0007g0108 a0001c0001t0007g0109 others(1): Show |
5 | HG03209.hp1 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+562A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438263 | |||||||
chr16:66438332 | C | T | 2 | a0001c0001t0003g0153 a0001c0001t0003g0278 |
2 | NA18963.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.25+631C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438332 | |||||||
chr16:66438333 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+632G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438333 | |||||||
chr16:66438345 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.25+644T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438345 | |||||||
chr16:66438375 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25+674C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438375 | |||||||
chr16:66438530 | C | T | 22 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0144 others(19): Show |
23 | HG00408.hp1 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.25+829C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438530 | |||||||
chr16:66438575 | C | T | 23 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0253 others(20): Show |
24 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+874C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438575 | |||||||
chr16:66438602 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0020 others(96): Show |
105 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.25+901G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438602 | |||||||
chr16:66438721 | T | C | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0032 others(83): Show |
91 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.25+1020T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438721 | |||||||
chr16:66438734 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.25+1033C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438734 | |||||||
chr16:66438806 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.25+1105C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438806 | |||||||
chr16:66438806 | C | T | 23 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0253 others(20): Show |
24 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.25+1105C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438806 | |||||||
chr16:66438809 | C | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0283 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+1108C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438809 | |||||||
chr16:66438811 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+1110C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66438811 | |||||||
chr16:66439485 | G | C | 69 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0036 others(66): Show |
74 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.25+1784G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439485 | |||||||
chr16:66439548 | C | T | 3 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0008g0006 |
4 | HG03209.hp1 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+1847C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439548 | |||||||
chr16:66439609 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0128 |
2 | HG01109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.25+1908G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439609 | |||||||
chr16:66439612 | G | GT | 71 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0032 others(68): Show |
76 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.25+1912dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66439612 | ||||||
chr16:66439723 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.25+2022G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439723 | |||||||
chr16:66439801 | G | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0283 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+2100G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439801 | |||||||
chr16:66439830 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0082 |
2 | HG03927.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.25+2129A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439830 | |||||||
chr16:66439838 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.25+2137C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439838 | |||||||
chr16:66439990 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0283 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+2289C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66439990 | |||||||
chr16:66440043 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+2342A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440043 | |||||||
chr16:66440123 | CT | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(124): Show |
133 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.25+2446delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66440123 | ||||||
chr16:66440123 | CTT | C | 69 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(66): Show |
75 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.25+2445_25+2446del others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66440123 | ||||||
chr16:66440123 | CTTT | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0221 a0001c0001t0001g0222 others(6): Show |
9 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+2444_25+2446del others(3): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66440123 | ||||||
chr16:66440129 | T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+2428T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440129 | |||||||
chr16:66440162 | C | A | 2 | a0001c0001t0001g0246 a0001c0001t0002g0251 |
2 | NA18942.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.25+2461C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440162 | |||||||
chr16:66440255 | A | G | 84 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0032 others(81): Show |
89 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.25+2554A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440255 | |||||||
chr16:66440369 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.25+2668G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440369 | |||||||
chr16:66440393 | A | G | 42 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0096 others(39): Show |
45 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.25+2692A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440393 | |||||||
chr16:66440572 | A | T | 6 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+2871A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440572 | |||||||
chr16:66440576 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+2875T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440576 | |||||||
chr16:66440594 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+2893G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440594 | |||||||
chr16:66440653 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+2952A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440653 | |||||||
chr16:66440717 | A | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3016A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440717 | |||||||
chr16:66440722 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3021A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440722 | |||||||
chr16:66440724 | T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3023T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440724 | |||||||
chr16:66440734 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3033G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440734 | |||||||
chr16:66440735 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3034G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440735 | |||||||
chr16:66440737 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3036T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440737 | |||||||
chr16:66440747 | T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3046T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440747 | |||||||
chr16:66440751 | T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3050T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440751 | |||||||
chr16:66440764 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3063T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440764 | |||||||
chr16:66440765 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3064G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440765 | |||||||
chr16:66440768 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3067T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440768 | |||||||
chr16:66440769 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3068G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440769 | |||||||
chr16:66440773 | T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3072T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440773 | |||||||
chr16:66440774 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3073G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440774 | |||||||
chr16:66440776 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3075G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440776 | |||||||
chr16:66440779 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3078G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440779 | |||||||
chr16:66440792 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3091A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440792 | |||||||
chr16:66440795 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3094T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440795 | |||||||
chr16:66440796 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3095G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440796 | |||||||
chr16:66440798 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3097G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440798 | |||||||
chr16:66440799 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3098T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440799 | |||||||
chr16:66440800 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3099T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440800 | |||||||
chr16:66440804 | A | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3103A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440804 | |||||||
chr16:66440805 | C | T | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+3104C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440805 | |||||||
chr16:66440808 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3107G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440808 | |||||||
chr16:66440811 | C | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3110C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440811 | |||||||
chr16:66440813 | A | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3112A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440813 | |||||||
chr16:66440814 | A | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3113A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440814 | |||||||
chr16:66440815 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3114A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440815 | |||||||
chr16:66440817 | T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3116T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440817 | |||||||
chr16:66440848 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3147T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440848 | |||||||
chr16:66440852 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3151T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440852 | |||||||
chr16:66440853 | T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3152T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440853 | |||||||
chr16:66440856 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3155T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440856 | |||||||
chr16:66440857 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3156T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440857 | |||||||
chr16:66440864 | T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3163T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440864 | |||||||
chr16:66440867 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3166T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440867 | |||||||
chr16:66440870 | T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3169T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440870 | |||||||
chr16:66440871 | T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3170T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440871 | |||||||
chr16:66440873 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3172G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440873 | |||||||
chr16:66440874 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3173G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440874 | |||||||
chr16:66440875 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3174G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440875 | |||||||
chr16:66440876 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3175G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440876 | |||||||
chr16:66440878 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3177G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440878 | |||||||
chr16:66440884 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3183G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440884 | |||||||
chr16:66440885 | T | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3184T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440885 | |||||||
chr16:66440886 | C | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3185C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440886 | |||||||
chr16:66440887 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3186A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440887 | |||||||
chr16:66440888 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3187G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440888 | |||||||
chr16:66440891 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3190A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440891 | |||||||
chr16:66440902 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3201A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440902 | |||||||
chr16:66440905 | C | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3204C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440905 | |||||||
chr16:66440908 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3207A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440908 | |||||||
chr16:66440909 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3208G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440909 | |||||||
chr16:66440916 | T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3215T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440916 | |||||||
chr16:66440934 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3233A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440934 | |||||||
chr16:66440975 | C | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3274C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440975 | |||||||
chr16:66440976 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3275T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66440976 | |||||||
chr16:66441011 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0283 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.25+3310G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441011 | |||||||
chr16:66441024 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3323G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441024 | |||||||
chr16:66441025 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3324A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441025 | |||||||
chr16:66441066 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3365G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441066 | |||||||
chr16:66441067 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3366T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441067 | |||||||
chr16:66441075 | T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3374T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441075 | |||||||
chr16:66441107 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3406A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441107 | |||||||
chr16:66441129 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3428G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441129 | |||||||
chr16:66441135 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3434A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441135 | |||||||
chr16:66441136 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3435G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441136 | |||||||
chr16:66441137 | T | G | 1 | a0001c0001t0002g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.25+3436T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441137 | |||||||
chr16:66441147 | C | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(192): Show |
206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.25+3446C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441147 | |||||||
chr16:66441251 | T | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+3550T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441251 | |||||||
chr16:66441353 | C | T | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+3652C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441353 | |||||||
chr16:66441505 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.25+3804C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441505 | |||||||
chr16:66441547 | C | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(193): Show |
207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.25+3846C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441547 | |||||||
chr16:66441712 | A | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0096 others(38): Show |
44 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.25+4011A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441712 | |||||||
chr16:66441873 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+4172C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441873 | |||||||
chr16:66441900 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(179): Show |
193 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.25+4199A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441900 | |||||||
chr16:66441941 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.25+4240A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441941 | |||||||
chr16:66441970 | C | G | 1 | a0001c0001t0002g0263 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.25+4269C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66441970 | |||||||
chr16:66442042 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.25+4341A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442042 | |||||||
chr16:66442160 | C | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0004g0002 others(7): Show |
13 | HG00738.hp1 HG02145.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.25+4459C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442160 | |||||||
chr16:66442172 | C | A | 5 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+4471C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442172 | |||||||
chr16:66442215 | G | T | 4 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+4514G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442215 | |||||||
chr16:66442474 | C | A | 5 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+4773C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442474 | |||||||
chr16:66442662 | A | AG | 5 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+4962dupG | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66442662 | ||||||
chr16:66442764 | T | G | 5 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+5063T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442764 | |||||||
chr16:66442770 | G | A | 5 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+5069G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442770 | |||||||
chr16:66442832 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+5131C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66442832 | |||||||
chr16:66443041 | C | T | 106 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(103): Show |
114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.25+5340C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443041 | |||||||
chr16:66443044 | T | C | 1 | a0001c0001t0002g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.25+5343T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443044 | |||||||
chr16:66443104 | G | C | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+5403G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443104 | |||||||
chr16:66443119 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.25+5418T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443119 | |||||||
chr16:66443186 | G | A | 4 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+5485G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443186 | |||||||
chr16:66443244 | T | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+5543T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443244 | |||||||
chr16:66443279 | T | C | 4 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+5578T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443279 | |||||||
chr16:66443610 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.25+5909C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443610 | |||||||
chr16:66443733 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.25+6032G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443733 | |||||||
chr16:66443796 | T | G | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+6095T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443796 | |||||||
chr16:66443818 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+6117G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443818 | |||||||
chr16:66443847 | C | T | 107 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(104): Show |
115 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.25+6146C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443847 | |||||||
chr16:66443907 | G | C | 106 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(103): Show |
114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.25+6206G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443907 | |||||||
chr16:66443976 | C | T | 9 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 others(6): Show |
9 | HG00673.hp1 HG02165.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+6275C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66443976 | |||||||
chr16:66444272 | A | G | 1 | a0003c0003t0002g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.25+6571A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444272 | |||||||
chr16:66444298 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.25+6597G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444298 | |||||||
chr16:66444391 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+6690C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444391 | |||||||
chr16:66444425 | G | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(181): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.25+6724G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444425 | |||||||
chr16:66444440 | G | A | 1 | a0001c0001t0003g0007 | 2 | NA18950.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.25+6739G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444440 | |||||||
chr16:66444528 | C | G | 1 | a0001c0001t0002g0079 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.25+6827C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444528 | |||||||
chr16:66444609 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.25+6908C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444609 | |||||||
chr16:66444834 | G | T | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+7133G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444834 | |||||||
chr16:66444999 | G | A | 2 | a0001c0001t0001g0260 a0001c0001t0001g0262 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.25+7298G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66444999 | |||||||
chr16:66445182 | A | G | 2 | a0001c0001t0003g0104 a0001c0001t0003g0106 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.25+7481A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445182 | |||||||
chr16:66445198 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+7497C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445198 | |||||||
chr16:66445293 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.25+7592G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445293 | |||||||
chr16:66445411 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+7710G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445411 | |||||||
chr16:66445475 | C | CA | 22 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(19): Show |
22 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.25+7814dupA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | C | CAA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0101 a0001c0001t0001g0178 others(4): Show |
7 | HG00738.hp2 HG01175.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+7813_25+7814dup others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CA | C | 18 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0053 others(15): Show |
18 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+7814delA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAA | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
7 | HG02486.hp2 HG02922.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+7813_25+7814del others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAA | C | 7 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0118 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7812_25+7814del others(3): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0001g0014 a0001c0001t0002g0120 a0001c0001t0002g0121 others(4): Show |
7 | HG01433.hp1 HG02109.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7803_25+7814del others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.25+7802_25+7814del others(13): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0267 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.25+7800_25+7814del others(15): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(9): Show |
C | 22 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(19): Show |
22 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.25+7799_25+7814del others(16): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(10): Show |
C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0043 others(52): Show |
58 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.25+7798_25+7814del others(17): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(11): Show |
C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0085 others(1): Show |
4 | HG02004.hp1 NA18747.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+7797_25+7814del others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(12): Show |
C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0204 others(3): Show |
6 | HG01109.hp1 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+7796_25+7814del others(19): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(13): Show |
C | 64 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(61): Show |
70 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.25+7795_25+7814del others(20): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(14): Show |
C | 15 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0129 others(12): Show |
17 | HG01109.hp2 HG02559.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.25+7794_25+7814del others(21): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445475 | CAAAAAAA others(15): Show |
C | 1 | a0001c0001t0001g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.25+7793_25+7814del others(22): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66445475 | ||||||
chr16:66445523 | G | A | 17 | a0001c0001t0001g0128 a0001c0001t0001g0253 a0001c0001t0001g0257 others(14): Show |
17 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.25+7822G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445523 | |||||||
chr16:66445549 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(180): Show |
194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.25+7848A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445549 | |||||||
chr16:66445577 | T | A | 1 | a0001c0001t0004g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.25+7876T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445577 | |||||||
chr16:66445653 | G | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0091 |
2 | HG00558.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.25+7952G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445653 | |||||||
chr16:66445749 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.25+8048C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445749 | |||||||
chr16:66445759 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(274): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.25+8058G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445759 | |||||||
chr16:66445797 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0043 others(73): Show |
79 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.25+8096G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445797 | |||||||
chr16:66445798 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+8097G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66445798 | |||||||
chr16:66446052 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.25+8351G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446052 | |||||||
chr16:66446057 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+8356C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446057 | |||||||
chr16:66446098 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+8397G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446098 | |||||||
chr16:66446205 | A | G | 3 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0164 |
3 | HG02615.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.25+8504A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446205 | |||||||
chr16:66446411 | A | G | 6 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02559.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+8710A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446411 | |||||||
chr16:66446412 | T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+8711T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446412 | |||||||
chr16:66446413 | A | G | 1 | a0001c0001t0002g0047 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.25+8712A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446413 | |||||||
chr16:66446526 | G | A | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(85): Show |
96 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.25+8825G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446526 | |||||||
chr16:66446841 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.25+9140C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446841 | |||||||
chr16:66446898 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+9197C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66446898 | |||||||
chr16:66447164 | G | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.25+9463G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447164 | |||||||
chr16:66447191 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.25+9490G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447191 | |||||||
chr16:66447198 | A | G | 3 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0164 |
3 | HG02615.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.25+9497A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447198 | |||||||
chr16:66447577 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+9876T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447577 | |||||||
chr16:66447642 | C | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0129 a0001c0001t0001g0131 others(2): Show |
5 | HG01109.hp2 HG03927.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+9941C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447642 | |||||||
chr16:66447927 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.25+10226A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447927 | |||||||
chr16:66447942 | A | G | 4 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0164 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+10241A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447942 | |||||||
chr16:66447965 | A | G | 3 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0164 |
3 | HG02615.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.25+10264A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66447965 | |||||||
chr16:66448158 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.25+10457C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448158 | |||||||
chr16:66448229 | T | TTTG | 188 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(185): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.25+10537_25+10539d others(5): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66448229 | ||||||
chr16:66448260 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0043 others(62): Show |
68 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.25+10559C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448260 | |||||||
chr16:66448271 | A | G | 3 | a0001c0001t0001g0246 a0001c0001t0001g0252 a0001c0001t0002g0251 |
3 | NA18942.hp2 NA18947.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.25+10570A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448271 | |||||||
chr16:66448363 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.25+10662G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448363 | |||||||
chr16:66448667 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+10966A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448667 | |||||||
chr16:66448690 | G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+10989G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448690 | |||||||
chr16:66448692 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0059 a0001c0001t0002g0061 |
3 | HG01257.hp1 HG01258.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.25+10991G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448692 | |||||||
chr16:66448770 | C | T | 18 | a0001c0001t0001g0128 a0001c0001t0001g0178 a0001c0001t0001g0253 others(15): Show |
18 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+11069C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448770 | |||||||
chr16:66448804 | G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+11103G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448804 | |||||||
chr16:66448808 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+11107C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66448808 | |||||||
chr16:66449459 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.25+11758T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449459 | |||||||
chr16:66449483 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(71): Show |
77 | HG00140.hp1 HG00280.hp2 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.25+11782T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449483 | |||||||
chr16:66449542 | T | G | 9 | a0001c0001t0001g0054 a0001c0001t0001g0062 a0001c0001t0001g0063 others(6): Show |
9 | HG02083.hp2 NA18612.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+11841T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449542 | |||||||
chr16:66449606 | C | CA | 60 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0054 others(57): Show |
63 | HG00140.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.25+11926dupA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66449606 | ||||||
chr16:66449606 | C | CAA | 26 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0086 others(23): Show |
26 | HG01256.hp2 HG02027.hp2 HG02486.hp2 others(23): Show |
intron_variant | MODIFIER | c.25+11925_25+11926d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66449606 | ||||||
chr16:66449606 | C | CAAA | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(84): Show |
95 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.25+11924_25+11926d others(5): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66449606 | ||||||
chr16:66449606 | C | CAAAA | 7 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0224 others(4): Show |
7 | HG00544.hp1 HG01109.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+11923_25+11926d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66449606 | ||||||
chr16:66449701 | A | G | 3 | a0001c0001t0003g0134 a0001c0001t0003g0142 a0001c0001t0003g0147 |
3 | NA18998.hp2 NA19005.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.25+12000A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449701 | |||||||
chr16:66449903 | C | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 others(89): Show |
99 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.25+12202C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449903 | |||||||
chr16:66449960 | G | T | 1 | a0001c0001t0003g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.25+12259G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66449960 | |||||||
chr16:66450041 | C | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(62): Show |
68 | HG00280.hp2 HG00673.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.25+12340C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450041 | |||||||
chr16:66450163 | T | C | 1 | a0001c0001t0002g0047 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.25+12462T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450163 | |||||||
chr16:66450219 | A | C | 1 | a0001c0001t0001g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.25+12518A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450219 | |||||||
chr16:66450291 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.25+12590C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450291 | |||||||
chr16:66450382 | T | G | 6 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02559.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+12681T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450382 | |||||||
chr16:66450733 | T | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(182): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.25+13032T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450733 | |||||||
chr16:66450826 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.25+13125G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66450826 | |||||||
chr16:66451069 | C | G | 1 | a0002c0002t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.25+13368C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451069 | |||||||
chr16:66451165 | A | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(61): Show |
67 | HG00280.hp2 HG00673.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.25+13464A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451165 | |||||||
chr16:66451236 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+13535C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451236 | |||||||
chr16:66451250 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.25+13549C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451250 | |||||||
chr16:66451426 | A | C | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+13725A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451426 | |||||||
chr16:66451579 | A | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(172): Show |
186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.25+13878A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451579 | |||||||
chr16:66451590 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(171): Show |
185 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.25+13889T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451590 | |||||||
chr16:66451639 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(62): Show |
68 | HG00280.hp2 HG00673.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.25+13938G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451639 | |||||||
chr16:66451685 | G | A | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+13984G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66451685 | |||||||
chr16:66452170 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.25+14469G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452170 | |||||||
chr16:66452236 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.25+14535T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452236 | |||||||
chr16:66452292 | G | C | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+14591G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452292 | |||||||
chr16:66452671 | A | G | 47 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0051 others(44): Show |
48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.25+14970A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452671 | |||||||
chr16:66452787 | CACTT | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0129 others(5): Show |
9 | HG01109.hp2 HG02559.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.25+15089_25+15092d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66452787 | ||||||
chr16:66452812 | G | A | 1 | a0001c0001t0003g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.25+15111G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452812 | |||||||
chr16:66452921 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+15220C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452921 | |||||||
chr16:66452921 | C | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0274 |
2 | HG00741.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.25+15220C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452921 | |||||||
chr16:66452927 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.25+15226A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66452927 | |||||||
chr16:66453022 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0036 others(136): Show |
144 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.25+15321A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453022 | |||||||
chr16:66453058 | A | C | 11 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(8): Show |
11 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.25+15357A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453058 | |||||||
chr16:66453085 | G | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(122): Show |
129 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.25+15384G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453085 | |||||||
chr16:66453110 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.25+15409G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453110 | |||||||
chr16:66453158 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0007g0108 a0001c0001t0007g0109 |
3 | HG03540.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.25+15457G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453158 | |||||||
chr16:66453303 | A | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(64): Show |
70 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.25+15602A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453303 | |||||||
chr16:66453342 | T | TAC | 53 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0051 others(50): Show |
54 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.25+15667_25+15668d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | ||||||
chr16:66453342 | T | TACAC | 7 | a0001c0001t0001g0180 a0001c0001t0001g0204 a0001c0001t0003g0163 others(4): Show |
7 | HG01175.hp2 HG01993.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.25+15665_25+15668d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | ||||||
chr16:66453342 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.25+15657_25+15668d others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | ||||||
chr16:66453342 | TACACAC | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.25+15663_25+15668d others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | ||||||
chr16:66453342 | TACACACA others(3): Show |
T | 2 | a0001c0001t0003g0114 a0001c0001t0003g0154 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.25+15659_25+15668d others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453342 | ||||||
chr16:66453731 | A | AT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.26-15859dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453731 | ||||||
chr16:66453731 | AT | A | 43 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0051 others(40): Show |
44 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.26-15859delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66453731 | ||||||
chr16:66453743 | T | G | 2 | a0001c0001t0001g0255 a0001c0001t0003g0163 |
2 | HG01934.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.26-15859T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453743 | |||||||
chr16:66453824 | T | C | 11 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(8): Show |
11 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-15778T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453824 | |||||||
chr16:66453939 | G | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.26-15663G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453939 | |||||||
chr16:66453960 | C | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(75): Show |
81 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.26-15642C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66453960 | |||||||
chr16:66454027 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0006g0284 a0001c0001t0009g0019 |
3 | HG02109.hp2 HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.26-15575G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454027 | |||||||
chr16:66454262 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-15340G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454262 | |||||||
chr16:66454649 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-14953T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454649 | |||||||
chr16:66454725 | C | G | 2 | a0001c0001t0007g0108 a0001c0001t0007g0109 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.26-14877C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454725 | |||||||
chr16:66454729 | C | CT | 32 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0033 others(29): Show |
35 | HG00280.hp1 HG00738.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.26-14853dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66454729 | ||||||
chr16:66454729 | CT | C | 38 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0038 others(35): Show |
39 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.26-14853delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66454729 | ||||||
chr16:66454729 | CTT | C | 16 | a0001c0001t0001g0046 a0001c0001t0001g0110 a0001c0001t0001g0111 others(13): Show |
16 | HG00558.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.26-14854_26-14853d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66454729 | ||||||
chr16:66454733 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26-14869T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66454733 | |||||||
chr16:66455202 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.26-14400G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455202 | |||||||
chr16:66455320 | A | C | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-14282A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455320 | |||||||
chr16:66455357 | A | C | 28 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0051 others(25): Show |
29 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.26-14245A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455357 | |||||||
chr16:66455416 | A | T | 1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-14186A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455416 | |||||||
chr16:66455458 | T | C | 1 | a0006c0004t0003g0197 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.26-14144T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455458 | |||||||
chr16:66455637 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-13965C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455637 | |||||||
chr16:66455671 | C | T | 3 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0164 |
3 | HG02615.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.26-13931C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455671 | |||||||
chr16:66455688 | C | CT | 44 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0038 others(41): Show |
46 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.26-13898dupT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66455688 | ||||||
chr16:66455688 | CT | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(113): Show |
122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.26-13898delT | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66455688 | ||||||
chr16:66455688 | CTT | C | 12 | a0001c0001t0001g0046 a0001c0001t0001g0094 a0001c0001t0001g0110 others(9): Show |
12 | HG01255.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-13899_26-13898d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66455688 | ||||||
chr16:66455842 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0046 others(63): Show |
69 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.26-13760A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455842 | |||||||
chr16:66455860 | T | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-13742T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66455860 | |||||||
chr16:66456134 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-13468G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456134 | |||||||
chr16:66456238 | G | A | 2 | a0001c0001t0006g0284 a0001c0001t0012g0105 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.26-13364G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456238 | |||||||
chr16:66456547 | G | A | 1 | a0004c0008t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.26-13055G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456547 | |||||||
chr16:66456691 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(67): Show |
73 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.26-12911T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456691 | |||||||
chr16:66456707 | G | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(8): Show |
12 | HG01069.hp2 HG01109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.26-12895G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456707 | |||||||
chr16:66456739 | A | C | 46 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0053 others(43): Show |
48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.26-12863A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456739 | |||||||
chr16:66456760 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.26-12842G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456760 | |||||||
chr16:66456790 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(68): Show |
74 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.26-12812G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66456790 | |||||||
chr16:66457013 | C | G | 56 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(53): Show |
57 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.26-12589C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457013 | |||||||
chr16:66457218 | G | T | 1 | a0001c0001t0002g0166 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.26-12384G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457218 | |||||||
chr16:66457336 | G | T | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.26-12266G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457336 | |||||||
chr16:66457423 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-12179C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457423 | |||||||
chr16:66457584 | C | T | 11 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-12018C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457584 | |||||||
chr16:66457707 | C | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0249 a0001c0001t0004g0012 |
4 | HG01069.hp2 HG01255.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-11895C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457707 | |||||||
chr16:66457785 | C | CA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(55): Show |
61 | HG00280.hp2 HG00673.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.26-11805dupA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66457785 | ||||||
chr16:66457785 | C | CAA | 7 | a0001c0001t0002g0060 a0001c0001t0002g0079 a0001c0001t0002g0090 others(4): Show |
7 | HG00558.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-11806_26-11805d others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66457785 | ||||||
chr16:66457887 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.26-11715G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66457887 | |||||||
chr16:66458027 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.26-11575G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458027 | |||||||
chr16:66458151 | C | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-11451C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458151 | |||||||
chr16:66458175 | T | C | 1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-11427T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458175 | |||||||
chr16:66458211 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0159 |
2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.26-11391A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458211 | |||||||
chr16:66458356 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.26-11246G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458356 | |||||||
chr16:66458466 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.26-11136C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458466 | |||||||
chr16:66458502 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0006g0284 |
2 | HG02886.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.26-11100G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458502 | |||||||
chr16:66458561 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
8 | HG01109.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-11041C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458561 | |||||||
chr16:66458589 | C | T | 2 | a0001c0001t0001g0259 a0001c0001t0001g0273 |
2 | HG00323.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.26-11013C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458589 | |||||||
chr16:66458626 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0003g0174 a0001c0001t0003g0195 |
3 | HG01256.hp1 HG01258.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.26-10976A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458626 | |||||||
chr16:66458650 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.26-10952T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458650 | |||||||
chr16:66458753 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(76): Show |
83 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-10849G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458753 | |||||||
chr16:66458884 | G | A | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-10718G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458884 | |||||||
chr16:66458985 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-10617T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66458985 | |||||||
chr16:66459181 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18980.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.26-10421A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459181 | |||||||
chr16:66459275 | C | T | 58 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(55): Show |
59 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.26-10327C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459275 | |||||||
chr16:66459445 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.26-10157G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459445 | |||||||
chr16:66459463 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.26-10139G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459463 | |||||||
chr16:66459653 | C | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG02486.hp1 HG02896.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.26-9949C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459653 | |||||||
chr16:66459666 | G | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-9936G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459666 | |||||||
chr16:66459746 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.26-9856T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459746 | |||||||
chr16:66459836 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.26-9766T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66459836 | |||||||
chr16:66460071 | G | C | 3 | a0001c0001t0001g0283 a0001c0001t0007g0108 a0001c0001t0007g0109 |
3 | HG02451.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.26-9531G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460071 | |||||||
chr16:66460101 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.26-9501T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460101 | |||||||
chr16:66460120 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.26-9482G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460120 | |||||||
chr16:66460155 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(76): Show |
83 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-9447T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460155 | |||||||
chr16:66460271 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0054 others(53): Show |
59 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.26-9331G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460271 | |||||||
chr16:66460428 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0165 |
2 | NA19003.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.26-9174G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460428 | |||||||
chr16:66460501 | G | A | 47 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0053 others(44): Show |
48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.26-9101G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66460501 | |||||||
chr16:66461192 | G | A | 1 | a0001c0001t0004g0012 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.26-8410G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461192 | |||||||
chr16:66461309 | C | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0061 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.26-8293C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461309 | |||||||
chr16:66461314 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.26-8288C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461314 | |||||||
chr16:66461320 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-8282C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461320 | |||||||
chr16:66461321 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.26-8281G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461321 | |||||||
chr16:66461366 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0004g0040 |
2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.26-8236G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461366 | |||||||
chr16:66461424 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0025 others(135): Show |
143 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.26-8178T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461424 | |||||||
chr16:66461462 | C | T | 1 | a0001c0001t0003g0140 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.26-8140C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461462 | |||||||
chr16:66461563 | G | A | 12 | a0001c0001t0001g0178 a0001c0001t0001g0257 a0001c0001t0001g0258 others(9): Show |
12 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-8039G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461563 | |||||||
chr16:66461569 | G | GAC | 12 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0023 others(9): Show |
13 | HG00323.hp1 HG01109.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-7989_26-7988dup others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | G | GACAC | 55 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0024 others(52): Show |
56 | HG00323.hp2 HG00408.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.26-7991_26-7988dup others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | G | GACACAC | 31 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0030 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.26-7993_26-7988dup others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | G | GACACACA others(1): Show |
6 | a0001c0001t0001g0132 a0001c0001t0001g0237 a0001c0001t0001g0238 others(3): Show |
6 | HG00609.hp2 HG00642.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-7995_26-7988dup others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | G | GACACACA others(3): Show |
11 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0209 others(8): Show |
14 | HG00544.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.26-7997_26-7988dup others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | G | GACACACA others(5): Show |
3 | a0001c0001t0001g0240 a0001c0001t0003g0174 a0001c0001t0003g0195 |
3 | HG01256.hp1 HG01258.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.26-7999_26-7988dup others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | G | GACACACA others(7): Show |
1 | a0001c0001t0002g0251 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.26-8001_26-7988dup others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | G | GACACACA others(9): Show |
1 | a0001c0001t0002g0243 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.26-8003_26-7988dup others(16): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | GAC | G | 20 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0128 others(17): Show |
22 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.26-7989_26-7988del others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | GACAC | G | 32 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0053 others(29): Show |
33 | HG00544.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.26-7991_26-7988del others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | GACACACA others(1): Show |
G | 5 | a0001c0001t0001g0283 a0001c0001t0003g0124 a0001c0001t0003g0163 others(2): Show |
5 | HG01993.hp1 HG02451.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-7995_26-7988del others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | GACACACA others(3): Show |
G | 1 | a0001c0001t0001g0144 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.26-7997_26-7988del others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | GACACACA others(5): Show |
G | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0249 others(6): Show |
10 | HG01069.hp2 HG01255.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-7999_26-7988del others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | GACACACA others(7): Show |
G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(67): Show |
73 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.26-8001_26-7988del others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461569 | GACACACA others(9): Show |
G | 2 | a0001c0001t0004g0004 a0001c0001t0009g0019 |
3 | HG00738.hp1 HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.26-8003_26-7988del others(16): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461569 | ||||||
chr16:66461613 | C | CACACACA others(4): Show |
1 | a0001c0001t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.26-7988_26-7987ins others(11): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66461613 | ||||||
chr16:66461615 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.26-7987A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461615 | |||||||
chr16:66461742 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.26-7860G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461742 | |||||||
chr16:66461765 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0005g0231 |
2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.26-7837T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461765 | |||||||
chr16:66461778 | A | C | 16 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0111 others(13): Show |
17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-7824A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461778 | |||||||
chr16:66461808 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-7794T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461808 | |||||||
chr16:66461885 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.26-7717C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461885 | |||||||
chr16:66461975 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.26-7627C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66461975 | |||||||
chr16:66462018 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.26-7584T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462018 | |||||||
chr16:66462158 | C | T | 47 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0053 others(44): Show |
48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.26-7444C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462158 | |||||||
chr16:66462196 | C | T | 16 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0111 others(13): Show |
17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-7406C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462196 | |||||||
chr16:66462444 | T | C | 1 | a0004c0008t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.26-7158T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462444 | |||||||
chr16:66462572 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0249 a0001c0001t0004g0012 |
4 | HG01069.hp2 HG01255.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-7030C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462572 | |||||||
chr16:66462573 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0003g0256 |
2 | HG04204.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.26-7029G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462573 | |||||||
chr16:66462658 | G | T | 1 | a0001c0001t0004g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.26-6944G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462658 | |||||||
chr16:66462687 | G | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0054 others(74): Show |
81 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.26-6915G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462687 | |||||||
chr16:66462731 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG01071.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.26-6871G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462731 | |||||||
chr16:66462755 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0186 a0001c0001t0001g0249 others(1): Show |
5 | HG01069.hp2 HG01255.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-6847C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462755 | |||||||
chr16:66462984 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0025 others(136): Show |
144 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.26-6618A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66462984 | |||||||
chr16:66463113 | A | T | 1 | a0001c0001t0003g0052 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.26-6489A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463113 | |||||||
chr16:66463114 | C | G | 1 | a0001c0001t0003g0052 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.26-6488C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463114 | |||||||
chr16:66463410 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.26-6192T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463410 | |||||||
chr16:66463510 | G | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-6092G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463510 | |||||||
chr16:66463591 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.26-6011G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463591 | |||||||
chr16:66463762 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.26-5840G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463762 | |||||||
chr16:66463947 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.26-5655G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66463947 | |||||||
chr16:66464037 | G | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0054 others(57): Show |
63 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.26-5565G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464037 | |||||||
chr16:66464126 | A | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(59): Show |
65 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.26-5476A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464126 | |||||||
chr16:66464156 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.26-5446C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464156 | |||||||
chr16:66464225 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.26-5377T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464225 | |||||||
chr16:66464399 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.26-5203T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464399 | |||||||
chr16:66464590 | G | A | 16 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0111 others(13): Show |
17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-5012G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464590 | |||||||
chr16:66464630 | A | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0249 |
2 | HG01069.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.26-4972A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464630 | |||||||
chr16:66464771 | T | C | 2 | a0001c0001t0001g0036 a0004c0008t0001g0050 |
2 | HG00609.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.26-4831T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464771 | |||||||
chr16:66464821 | T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-4781T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464821 | |||||||
chr16:66464925 | G | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0233 a0001c0001t0001g0235 |
3 | HG02683.hp1 HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.26-4677G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464925 | |||||||
chr16:66464997 | G | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0054 others(48): Show |
54 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.26-4605G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66464997 | |||||||
chr16:66465231 | G | A | 16 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0111 others(13): Show |
17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-4371G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465231 | |||||||
chr16:66465319 | C | T | 2 | a0003c0003t0002g0080 a0003c0003t0002g0158 |
2 | NA19007.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.26-4283C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465319 | |||||||
chr16:66465456 | T | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-4146T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465456 | |||||||
chr16:66465508 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0054 others(76): Show |
83 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.26-4094G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465508 | |||||||
chr16:66465577 | G | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-4025G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465577 | |||||||
chr16:66465672 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.26-3930T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465672 | |||||||
chr16:66465722 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(77): Show |
84 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.26-3880C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66465722 | |||||||
chr16:66465975 | GCTAA | G | 3 | a0001c0001t0001g0283 a0001c0001t0007g0108 a0001c0001t0007g0109 |
3 | HG02451.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.26-3624_26-3621del others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66465975 | ||||||
chr16:66466066 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.26-3536G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466066 | |||||||
chr16:66466104 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0226 a0001c0001t0001g0230 |
4 | HG00323.hp1 HG00733.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-3498G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466104 | |||||||
chr16:66466109 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-3493C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466109 | |||||||
chr16:66466263 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.26-3339C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466263 | |||||||
chr16:66466294 | A | C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-3308A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466294 | |||||||
chr16:66466309 | C | A | 1 | a0001c0001t0002g0213 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.26-3293C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466309 | |||||||
chr16:66466398 | TTC | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.26-3198_26-3197del others(2): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr16 | 66466398 | ||||||
chr16:66466600 | T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-3002T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466600 | |||||||
chr16:66466781 | C | T | 16 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0111 others(13): Show |
17 | HG01069.hp2 HG01255.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.26-2821C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66466781 | |||||||
chr16:66467045 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0249 |
2 | HG01069.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.26-2557T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467045 | |||||||
chr16:66467307 | A | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0043 others(58): Show |
64 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.26-2295A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467307 | |||||||
chr16:66467335 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.26-2267C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467335 | |||||||
chr16:66467362 | C | T | 1 | a0001c0001t0003g0142 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.26-2240C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467362 | |||||||
chr16:66467389 | G | A | 1 | a0001c0001t0003g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.26-2213G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467389 | |||||||
chr16:66467390 | G | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-2212G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467390 | |||||||
chr16:66467442 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.26-2160C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467442 | |||||||
chr16:66467515 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-2087C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467515 | |||||||
chr16:66467555 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.26-2047C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467555 | |||||||
chr16:66467593 | G | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0015 others(44): Show |
50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.26-2009G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467593 | |||||||
chr16:66467731 | G | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1871G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467731 | |||||||
chr16:66467816 | G | A | 13 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(10): Show |
13 | HG02486.hp2 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.26-1786G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467816 | |||||||
chr16:66467877 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.26-1725C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66467877 | |||||||
chr16:66468109 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.26-1493G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468109 | |||||||
chr16:66468234 | T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1368T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468234 | |||||||
chr16:66468257 | A | C | 7 | a0001c0001t0004g0002 a0001c0001t0004g0004 a0001c0001t0004g0005 others(4): Show |
10 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-1345A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468257 | |||||||
chr16:66468257 | A | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1345A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468257 | |||||||
chr16:66468354 | G | C | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG01071.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.26-1248G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468354 | |||||||
chr16:66468478 | C | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-1124C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468478 | |||||||
chr16:66468515 | A | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1087A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468515 | |||||||
chr16:66468576 | C | T | 5 | a0001c0001t0002g0115 a0001c0001t0002g0117 a0001c0001t0002g0121 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-1026C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468576 | |||||||
chr16:66468585 | G | T | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-1017G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468585 | |||||||
chr16:66468588 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.26-1014G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468588 | |||||||
chr16:66468605 | C | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.26-997C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468605 | |||||||
chr16:66468674 | A | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-928A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468674 | |||||||
chr16:66468730 | C | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.26-872C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468730 | |||||||
chr16:66468873 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.26-729C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468873 | |||||||
chr16:66468893 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.26-709A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468893 | |||||||
chr16:66468946 | A | C | 1 | a0001c0001t0003g0147 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.26-656A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66468946 | |||||||
chr16:66469101 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.26-501A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469101 | |||||||
chr16:66469148 | C | T | 47 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0053 others(44): Show |
48 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.26-454C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469148 | |||||||
chr16:66469270 | C | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.26-332C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469270 | |||||||
chr16:66469362 | C | A | 1 | a0001c0001t0001g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-240C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469362 | |||||||
chr16:66469477 | G | A | 8 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(5): Show |
8 | HG02486.hp2 HG02559.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-125G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469477 | |||||||
chr16:66469536 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.26-66G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 2/4 | chr16 | 66469536 | |||||||
chr16:66469875 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
8 | HG01109.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+10C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66469875 | |||||||
chr16:66469972 | G | A | 12 | a0001c0001t0001g0178 a0001c0001t0001g0257 a0001c0001t0001g0258 others(9): Show |
12 | HG00323.hp2 HG00642.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.289+107G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66469972 | |||||||
chr16:66469979 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.289+114C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66469979 | |||||||
chr16:66470170 | C | CGATG | 69 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0015 others(66): Show |
71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.289+351_289+354dup others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | ||||||
chr16:66470170 | C | CGATGGAT others(1): Show |
7 | a0001c0001t0001g0030 a0001c0001t0001g0107 a0001c0001t0001g0178 others(4): Show |
7 | HG02004.hp2 HG02809.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.289+347_289+354dup others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | ||||||
chr16:66470170 | C | CGATGGAT others(5): Show |
1 | a0001c0001t0001g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.289+343_289+354dup others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | ||||||
chr16:66470170 | CGATG | C | 13 | a0001c0001t0001g0096 a0001c0001t0001g0177 a0001c0001t0001g0249 others(10): Show |
16 | HG00609.hp1 HG00735.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.289+351_289+354del others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | ||||||
chr16:66470170 | CGATGGAT others(1): Show |
C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(9): Show |
12 | HG01109.hp2 HG01175.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+347_289+354del others(8): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | ||||||
chr16:66470170 | CGATGGAT others(5): Show |
C | 45 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0053 others(42): Show |
46 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.289+343_289+354del others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66470170 | ||||||
chr16:66470870 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.289+1005T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66470870 | |||||||
chr16:66470989 | C | G | 1 | a0001c0001t0001g0201 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.289+1124C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66470989 | |||||||
chr16:66471435 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0025 others(138): Show |
146 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.289+1570A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471435 | |||||||
chr16:66471440 | G | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.289+1575G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471440 | |||||||
chr16:66471464 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0009g0019 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.289+1599G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471464 | |||||||
chr16:66471549 | T | G | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.289+1684T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471549 | |||||||
chr16:66471666 | A | G | 2 | a0001c0001t0006g0284 a0001c0001t0009g0019 |
2 | HG02109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.289+1801A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471666 | |||||||
chr16:66471676 | T | C | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.289+1811T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471676 | |||||||
chr16:66471812 | A | G | 11 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+1947A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471812 | |||||||
chr16:66471816 | C | T | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289+1951C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471816 | |||||||
chr16:66471911 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.289+2046G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66471911 | |||||||
chr16:66472124 | C | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.289+2259C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472124 | |||||||
chr16:66472346 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.289+2481A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472346 | |||||||
chr16:66472478 | C | T | 2 | a0001c0001t0003g0114 a0001c0001t0003g0154 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.289+2613C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472478 | |||||||
chr16:66472755 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0249 a0001c0001t0004g0012 |
4 | HG01069.hp2 HG01255.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+2890C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472755 | |||||||
chr16:66472786 | A | G | 66 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0043 others(63): Show |
68 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.289+2921A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472786 | |||||||
chr16:66472875 | A | T | 1 | a0001c0001t0001g0258 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.289+3010A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472875 | |||||||
chr16:66472886 | A | G | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.289+3021A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472886 | |||||||
chr16:66472948 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.289+3083G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66472948 | |||||||
chr16:66473039 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.289+3174T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473039 | |||||||
chr16:66473173 | T | C | 126 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(123): Show |
130 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.289+3308T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473173 | |||||||
chr16:66473207 | G | A | 48 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0053 others(45): Show |
50 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.289+3342G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473207 | |||||||
chr16:66473311 | C | G | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.289+3446C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473311 | |||||||
chr16:66473346 | G | T | 1 | a0001c0001t0003g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.289+3481G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473346 | |||||||
chr16:66473382 | C | T | 2 | a0001c0001t0003g0160 a0001c0001t0003g0161 |
2 | NA19012.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.289+3517C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473382 | |||||||
chr16:66473505 | G | A | 4 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0003c0003t0002g0080 others(1): Show |
4 | NA18953.hp1 NA19007.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.289+3640G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473505 | |||||||
chr16:66473511 | C | T | 11 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(8): Show |
11 | HG02486.hp2 HG02559.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.289+3646C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473511 | |||||||
chr16:66473551 | A | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
14 | HG00323.hp1 HG00733.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.289+3686A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473551 | |||||||
chr16:66473556 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0004g0040 |
2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.289+3691G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473556 | |||||||
chr16:66473696 | CTAAATAA others(9): Show |
C | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289+3843_290-3837d others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66473696 | ||||||
chr16:66473720 | A | T | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG01169.hp2 HG01934.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.290-3840A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473720 | |||||||
chr16:66473721 | T | A | 10 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG01169.hp2 HG01934.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.290-3839T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473721 | |||||||
chr16:66473869 | G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-3691G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66473869 | |||||||
chr16:66474070 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.290-3490C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474070 | |||||||
chr16:66474322 | T | A | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290-3238T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474322 | |||||||
chr16:66474443 | T | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-3117T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474443 | |||||||
chr16:66474544 | A | AAGAGGGA others(5): Show |
3 | a0001c0001t0001g0064 a0001c0001t0001g0222 a0001c0001t0001g0240 |
3 | NA18969.hp1 NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.290-2979_290-2968d others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | ||||||
chr16:66474544 | A | AAGAGGGA others(17): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0236 |
2 | HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.290-2991_290-2968d others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | ||||||
chr16:66474544 | A | AAGAGGGA others(81): Show |
1 | a0001c0001t0004g0012 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.290-2992_290-2991i others(90): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | ||||||
chr16:66474544 | A | AAGAGGGA others(85): Show |
1 | a0001c0001t0002g0039 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(94): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | ||||||
chr16:66474544 | A | AAGAGGGA others(25): Show |
1 | a0001c0001t0002g0216 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.290-3004_290-3003i others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | ||||||
chr16:66474544 | AAGAGGGA others(53): Show |
A | 1 | a0001c0001t0002g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.290-3003_290-2944d others(62): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474544 | ||||||
chr16:66474545 | A | AGAGGGAG others(17): Show |
1 | a0001c0001t0001g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.290-2992_290-2991i others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474545 | ||||||
chr16:66474557 | A | AGAGGGAG others(1): Show |
6 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0129 others(3): Show |
6 | HG01109.hp2 HG02622.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-2999_290-2992d others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | ||||||
chr16:66474557 | A | AGAGGGAG others(29): Show |
2 | a0001c0001t0001g0189 a0001c0001t0001g0201 |
2 | NA18953.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.290-2979_290-2944d others(38): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | ||||||
chr16:66474557 | A | AGAGGGAG others(5): Show |
1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | ||||||
chr16:66474557 | A | AGAGGGAG others(9): Show |
1 | a0001c0001t0001g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | ||||||
chr16:66474557 | A | AGAGGGAG others(65): Show |
1 | a0001c0001t0001g0208 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(74): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474557 | ||||||
chr16:66474561 | G | GGAGGGAG others(9): Show |
1 | a0001c0001t0001g0027 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.290-2992_290-2991i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474561 | ||||||
chr16:66474562 | G | GAGGGAGA others(25): Show |
1 | a0001c0001t0001g0285 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.290-2984_290-2983i others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474562 | ||||||
chr16:66474569 | A | AGAGGGAG others(13): Show |
1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.290-2979_290-2960d others(22): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474569 | A | AGAGGGAG others(45): Show |
1 | a0001c0005t0001g0200 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.290-2968_290-2967i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474569 | A | AGAGGGAG others(25): Show |
3 | a0001c0001t0001g0178 a0001c0001t0001g0267 a0001c0001t0001g0268 |
3 | HG00642.hp2 HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.290-2987_290-2956d others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474569 | A | AGAGGGAG others(77): Show |
1 | a0001c0001t0001g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.290-2910_290-2909i others(86): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474569 | A | AGAGGGAG others(5): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0168 |
2 | HG03927.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.290-2980_290-2979i others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474569 | A | AGAGGGAG others(453): Show |
1 | a0001c0001t0001g0036 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.290-2980_290-2979i others(462): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474569 | A | AGAGGGAG others(77): Show |
1 | a0001c0001t0001g0022 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290-2980_290-2979i others(86): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474569 | A | AGAGGGAG others(165): Show |
2 | a0001c0001t0001g0033 a0001c0001t0004g0040 |
2 | HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.290-2980_290-2979i others(174): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474569 | A | AGAGGGAG others(45): Show |
1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.290-2980_290-2979i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474569 | A | G | 17 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0110 others(14): Show |
17 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.290-2991A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474569 | |||||||
chr16:66474569 | AGAGG | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG02630.hp2 HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.290-2983_290-2980d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474569 | ||||||
chr16:66474570 | G | GAGGGAGG others(29): Show |
1 | a0001c0001t0007g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290-2980_290-2979i others(38): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474570 | ||||||
chr16:66474573 | GGAGGGAG others(1): Show |
G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0095 others(9): Show |
13 | HG00621.hp2 HG00673.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.290-2979_290-2972d others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474573 | ||||||
chr16:66474574 | G | GAGGGAGG others(17): Show |
1 | a0001c0001t0003g0275 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.290-2980_290-2979i others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474574 | ||||||
chr16:66474577 | GGAGA | G | 6 | a0001c0001t0004g0002 a0001c0001t0004g0004 a0001c0001t0004g0005 others(3): Show |
9 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-2979_290-2976d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474577 | ||||||
chr16:66474577 | GGAGAGAG others(21): Show |
G | 1 | a0001c0001t0001g0133 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.290-2979_290-2952d others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474577 | ||||||
chr16:66474581 | A | AGAGGGAG others(34): Show |
1 | a0001c0001t0001g0191 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.290-2968_290-2967i others(43): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474581 | ||||||
chr16:66474581 | A | AGAGGGAG others(217): Show |
1 | a0001c0001t0005g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.290-2968_290-2967i others(226): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474581 | ||||||
chr16:66474581 | A | AGAGGGAG others(5): Show |
1 | a0001c0001t0001g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.290-2967_290-2956d others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474581 | ||||||
chr16:66474581 | A | G | 21 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
21 | HG00609.hp1 HG00621.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.290-2979A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474581 | |||||||
chr16:66474589 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.290-2971G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474589 | |||||||
chr16:66474590 | G | A | 1 | a0001c0001t0003g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.290-2970G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474590 | |||||||
chr16:66474590 | G | GAGGA | 6 | a0001c0001t0001g0053 a0001c0001t0003g0114 a0001c0001t0003g0141 others(3): Show |
6 | HG00621.hp1 HG02015.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.290-2967_290-2966i others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474590 | ||||||
chr16:66474593 | G | A | 46 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0062 others(43): Show |
48 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.290-2967G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474593 | |||||||
chr16:66474594 | G | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0252 a0001c0001t0003g0114 others(6): Show |
9 | HG00621.hp1 HG02015.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-2966G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474594 | |||||||
chr16:66474598 | G | A | 10 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0002g0039 others(7): Show |
13 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.290-2962G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474598 | |||||||
chr16:66474601 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0167 others(6): Show |
10 | HG00621.hp2 HG00673.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.290-2959G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474601 | |||||||
chr16:66474601 | GGAGA | G | 6 | a0001c0001t0003g0137 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG00733.hp1 HG01099.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-2955_290-2952d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474601 | ||||||
chr16:66474602 | G | A | 20 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0053 others(17): Show |
23 | HG00621.hp1 HG00738.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.290-2958G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474602 | |||||||
chr16:66474602 | G | GAGGAAGG others(1): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0217 a0001c0001t0004g0041 others(1): Show |
4 | HG02145.hp2 HG03041.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-2956_290-2955i others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474602 | ||||||
chr16:66474602 | G | GAGGAAGG others(9): Show |
5 | a0001c0001t0003g0007 a0001c0001t0003g0142 a0001c0001t0003g0147 others(2): Show |
6 | NA18950.hp1 NA18968.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-2956_290-2955i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474602 | ||||||
chr16:66474602 | G | GAGGAAGG others(89): Show |
1 | a0001c0001t0001g0204 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.290-2956_290-2955i others(98): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474602 | ||||||
chr16:66474603 | A | AGGAAGGA others(3): Show |
4 | a0001c0001t0003g0123 a0001c0001t0003g0150 a0001c0001t0003g0176 others(1): Show |
4 | HG02723.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2956_290-2955i others(12): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474603 | ||||||
chr16:66474605 | A | AGAGGGAG others(117): Show |
1 | a0001c0001t0003g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(126): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474605 | ||||||
chr16:66474605 | A | AGAGGGAG others(9): Show |
1 | a0001c0001t0003g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474605 | ||||||
chr16:66474605 | A | G | 93 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0025 others(90): Show |
100 | HG00280.hp2 HG00544.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.290-2955A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474605 | |||||||
chr16:66474606 | G | A | 19 | a0001c0001t0001g0031 a0001c0001t0001g0129 a0001c0001t0001g0208 others(16): Show |
20 | HG00609.hp1 HG02257.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.290-2954G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474606 | |||||||
chr16:66474606 | G | GAGGGAGG others(29): Show |
1 | a0001c0001t0003g0250 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.290-2943_290-2942i others(38): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474606 | ||||||
chr16:66474606 | G | GAGGGAGG others(121): Show |
1 | a0001c0001t0001g0034 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(130): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474606 | ||||||
chr16:66474606 | G | GGA | 4 | a0001c0001t0003g0123 a0001c0001t0003g0150 a0001c0001t0003g0176 others(1): Show |
4 | HG02723.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2954_290-2953i others(4): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474606 | |||||||
chr16:66474610 | G | A | 37 | a0001c0001t0001g0027 a0001c0001t0001g0118 a0001c0001t0001g0119 others(34): Show |
41 | HG00609.hp1 HG00733.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.290-2950G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474610 | |||||||
chr16:66474610 | G | GAGGGAGA others(141): Show |
1 | a0001c0001t0002g0279 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(150): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | ||||||
chr16:66474610 | G | GAGGGAGA others(129): Show |
1 | a0001c0001t0002g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(138): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | ||||||
chr16:66474610 | G | GAGGGAGA others(149): Show |
1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(158): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | ||||||
chr16:66474610 | G | GAGGGAGA others(33): Show |
1 | a0001c0001t0001g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(42): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | ||||||
chr16:66474610 | G | GAGGGAGG others(13): Show |
1 | a0001c0001t0002g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(22): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | ||||||
chr16:66474610 | G | GAGGGAGG others(21): Show |
1 | a0001c0001t0002g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.290-2943_290-2942i others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474610 | ||||||
chr16:66474614 | G | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0031 others(15): Show |
19 | HG00323.hp2 HG00621.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.290-2946G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474614 | |||||||
chr16:66474614 | G | GAGAGAGG others(141): Show |
1 | a0001c0001t0002g0003 | 2 | HG01975.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.290-2944_290-2943i others(150): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGAGAGG others(57): Show |
1 | a0001c0001t0001g0274 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(66): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGAGAGG others(49): Show |
1 | a0001c0001t0003g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(58): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGAGAGG others(37): Show |
1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(46): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGAGAGG others(101): Show |
1 | a0001c0001t0001g0257 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.290-2944_290-2943i others(110): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGAGAGG others(33): Show |
6 | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0177 others(3): Show |
6 | HG00408.hp2 HG02083.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-2944_290-2943i others(42): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGAGAGG others(33): Show |
1 | a0001c0001t0003g0124 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(42): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGGGAGG others(105): Show |
1 | a0001c0001t0001g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(114): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGGGAGG others(21): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0082 a0001c0001t0001g0096 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.290-2943_290-2942i others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGGGAGG others(117): Show |
5 | a0001c0001t0002g0115 a0001c0001t0002g0117 a0001c0001t0002g0121 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.290-2943_290-2942i others(126): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474614 | G | GAGGGAGG others(141): Show |
1 | a0001c0001t0001g0249 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.290-2943_290-2942i others(150): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474614 | ||||||
chr16:66474616 | G | GAGGAGGG others(254): Show |
1 | a0001c0001t0002g0092 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.290-2944_290-2943i others(263): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474616 | |||||||
chr16:66474616 | G | GGGAGGGA others(169): Show |
2 | a0001c0001t0003g0104 a0001c0001t0003g0106 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.290-2943_290-2942i others(178): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474616 | ||||||
chr16:66474618 | A | AAGGAAGG others(9): Show |
3 | a0001c0001t0001g0101 a0001c0001t0001g0186 a0001c0001t0002g0099 |
3 | HG03669.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.290-2939_290-2938i others(18): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGAAGG others(13): Show |
4 | a0001c0001t0001g0131 a0001c0001t0001g0180 a0001c0001t0003g0155 others(1): Show |
4 | HG01169.hp1 HG02602.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2939_290-2938i others(22): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGAAGG others(17): Show |
2 | a0001c0001t0001g0051 a0001c0001t0008g0006 |
3 | HG03209.hp1 HG03453.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.290-2939_290-2938i others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGAAGG others(25): Show |
1 | a0001c0001t0003g0163 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.290-2939_290-2938i others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGG | 101 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(98): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.290-2913_290-2910d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(1): Show |
9 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(6): Show |
9 | HG00140.hp1 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-2917_290-2910d others(10): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(5): Show |
3 | a0001c0001t0003g0175 a0001c0001t0003g0198 a0001c0001t0003g0199 |
3 | HG02896.hp2 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.290-2933_290-2932i others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(189): Show |
1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.290-2920_290-2919i others(198): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(109): Show |
1 | a0001c0001t0001g0085 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.290-2920_290-2919i others(118): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(25): Show |
1 | a0001c0001t0001g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.290-2941_290-2910d others(34): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(45): Show |
2 | a0001c0001t0001g0173 a0001c0001t0001g0248 |
2 | HG02258.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.290-2910_290-2909i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(45): Show |
1 | a0004c0008t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.290-2910_290-2909i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(137): Show |
2 | a0001c0001t0001g0224 a0001c0001t0001g0254 |
2 | HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.290-2910_290-2909i others(146): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(45): Show |
1 | a0002c0002t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.290-2910_290-2909i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | AAGGGAGG others(85): Show |
4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0136 others(1): Show |
4 | HG01928.hp2 HG01943.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2910_290-2909i others(94): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474618 | ||||||
chr16:66474618 | A | G | 117 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0021 others(114): Show |
124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.290-2942A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474618 | |||||||
chr16:66474621 | G | GGAGGGAG others(169): Show |
1 | a0001c0001t0002g0213 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.290-2920_290-2919i others(178): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474621 | ||||||
chr16:66474621 | G | GGAGGGAG others(85): Show |
1 | a0001c0001t0001g0170 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.290-2910_290-2909i others(94): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474621 | ||||||
chr16:66474622 | G | A | 8 | a0001c0001t0001g0101 a0001c0001t0002g0003 a0001c0001t0002g0060 others(5): Show |
9 | HG01975.hp1 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.290-2938G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474622 | |||||||
chr16:66474622 | G | GAGGA | 4 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0002g0097 others(1): Show |
4 | HG02622.hp2 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2935_290-2934i others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | ||||||
chr16:66474622 | G | GAGGAAGG others(17): Show |
14 | a0001c0001t0001g0157 a0001c0001t0002g0018 a0001c0001t0002g0045 others(11): Show |
14 | HG00280.hp2 HG00544.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.290-2935_290-2934i others(26): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | ||||||
chr16:66474622 | G | GAGGAAGG others(77): Show |
1 | a0001c0001t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.290-2935_290-2934i others(86): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | ||||||
chr16:66474622 | G | GAGGAAGG others(5): Show |
1 | a0001c0001t0002g0216 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.290-2935_290-2934i others(14): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | ||||||
chr16:66474622 | G | GAGGAAGG others(45): Show |
1 | a0001c0001t0002g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.290-2935_290-2934i others(54): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | ||||||
chr16:66474622 | G | GAGGAGGA others(19): Show |
1 | a0001c0001t0002g0044 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.290-2935_290-2934i others(28): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | ||||||
chr16:66474622 | G | GAGGGAGG others(21): Show |
1 | a0001c0001t0002g0073 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.290-2931_290-2930i others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | ||||||
chr16:66474622 | G | GAGGGAGG others(29): Show |
4 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0003c0003t0002g0080 others(1): Show |
4 | HG00558.hp1 HG03831.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-2923_290-2922i others(38): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474622 | ||||||
chr16:66474626 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.290-2934G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474626 | |||||||
chr16:66474629 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0201 |
2 | NA18953.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.290-2931G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474629 | |||||||
chr16:66474637 | G | GGAGGGAG others(21): Show |
3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG01071.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.290-2910_290-2909i others(30): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474637 | ||||||
chr16:66474638 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.290-2922G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474638 | |||||||
chr16:66474639 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.290-2921A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474639 | |||||||
chr16:66474691 | G | C | 1 | a0001c0001t0001g0017 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.290-2869G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474691 | |||||||
chr16:66474730 | AAAAGAAA others(8): Show |
A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0239 |
2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.290-2821_290-2807d others(17): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474730 | ||||||
chr16:66474743 | GAGAA | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0009g0019 others(1): Show |
4 | HG02071.hp2 HG02074.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.290-2800_290-2797d others(6): Show |
BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66474743 | ||||||
chr16:66474918 | G | A | 1 | a0006c0004t0003g0197 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.290-2642G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474918 | |||||||
chr16:66474965 | A | T | 1 | a0001c0001t0002g0092 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.290-2595A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66474965 | |||||||
chr16:66475056 | G | A | 2 | a0001c0001t0003g0153 a0001c0001t0003g0278 |
2 | NA18963.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.290-2504G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475056 | |||||||
chr16:66475079 | G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-2481G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475079 | |||||||
chr16:66475167 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.290-2393C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475167 | |||||||
chr16:66475222 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(274): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.290-2338A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475222 | |||||||
chr16:66475371 | C | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.290-2189C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475371 | |||||||
chr16:66475748 | A | G | 7 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0068 others(4): Show |
8 | HG01975.hp1 HG02071.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-1812A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475748 | |||||||
chr16:66475784 | T | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0227 |
2 | NA18955.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.290-1776T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475784 | |||||||
chr16:66475937 | G | C | 1 | a0001c0001t0001g0242 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.290-1623G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66475937 | |||||||
chr16:66476042 | G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-1518G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476042 | |||||||
chr16:66476109 | CA | C | 60 | a0001c0001t0001g0113 a0001c0001t0001g0236 a0001c0001t0002g0003 others(57): Show |
66 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.290-1436delA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66476109 | ||||||
chr16:66476121 | A | G | 11 | a0001c0001t0004g0002 a0001c0001t0004g0004 a0001c0001t0004g0005 others(8): Show |
15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.290-1439A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476121 | |||||||
chr16:66476250 | G | A | 59 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0018 others(56): Show |
65 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.290-1310G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476250 | |||||||
chr16:66476275 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.290-1285G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476275 | |||||||
chr16:66476445 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1115G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476445 | |||||||
chr16:66476447 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1113A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476447 | |||||||
chr16:66476448 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1112A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476448 | |||||||
chr16:66476450 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1110T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476450 | |||||||
chr16:66476451 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1109G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476451 | |||||||
chr16:66476456 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1104A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476456 | |||||||
chr16:66476458 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1102T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476458 | |||||||
chr16:66476460 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1100A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476460 | |||||||
chr16:66476462 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1098A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476462 | |||||||
chr16:66476465 | A | G | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.290-1095A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476465 | |||||||
chr16:66476466 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1094G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476466 | |||||||
chr16:66476467 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1093A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476467 | |||||||
chr16:66476468 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1092G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476468 | |||||||
chr16:66476469 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1091A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476469 | |||||||
chr16:66476470 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1090A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476470 | |||||||
chr16:66476471 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1089A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476471 | |||||||
chr16:66476472 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1088G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476472 | |||||||
chr16:66476473 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1087G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476473 | |||||||
chr16:66476477 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1083T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476477 | |||||||
chr16:66476478 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1082A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476478 | |||||||
chr16:66476479 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1081G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476479 | |||||||
chr16:66476481 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1079T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476481 | |||||||
chr16:66476483 | C | A | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1077C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476483 | |||||||
chr16:66476484 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1076G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476484 | |||||||
chr16:66476492 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1068T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476492 | |||||||
chr16:66476493 | G | A | 2 | a0001c0001t0006g0284 a0001c0001t0012g0105 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.290-1067G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476493 | |||||||
chr16:66476498 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1062G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476498 | |||||||
chr16:66476503 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1057A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476503 | |||||||
chr16:66476504 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1056C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476504 | |||||||
chr16:66476509 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1051A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476509 | |||||||
chr16:66476511 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1049A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476511 | |||||||
chr16:66476512 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1048G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476512 | |||||||
chr16:66476513 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1047G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476513 | |||||||
chr16:66476514 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1046G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476514 | |||||||
chr16:66476515 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1045G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476515 | |||||||
chr16:66476516 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1044A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476516 | |||||||
chr16:66476517 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1043G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476517 | |||||||
chr16:66476518 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1042G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476518 | |||||||
chr16:66476519 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1041A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476519 | |||||||
chr16:66476520 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1040G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476520 | |||||||
chr16:66476521 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1039G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476521 | |||||||
chr16:66476523 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1037A>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476523 | |||||||
chr16:66476526 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1034T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476526 | |||||||
chr16:66476527 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1033G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476527 | |||||||
chr16:66476529 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1031G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476529 | |||||||
chr16:66476530 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1030A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476530 | |||||||
chr16:66476531 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1029G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476531 | |||||||
chr16:66476535 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1025T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476535 | |||||||
chr16:66476536 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1024G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476536 | |||||||
chr16:66476537 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1023G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476537 | |||||||
chr16:66476543 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.290-1017G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476543 | |||||||
chr16:66476551 | C | G | 1 | a0001c0001t0002g0047 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.290-1009C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476551 | |||||||
chr16:66476878 | T | TA | 11 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0086 others(8): Show |
11 | HG00140.hp1 HG00140.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.290-676dupA | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr16 | 66476878 | ||||||
chr16:66476926 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.290-634T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66476926 | |||||||
chr16:66477126 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.290-434C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477126 | |||||||
chr16:66477142 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.290-418C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477142 | |||||||
chr16:66477186 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.290-374C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477186 | |||||||
chr16:66477281 | G | A | 3 | a0001c0001t0001g0259 a0001c0001t0003g0153 a0001c0001t0003g0278 |
3 | HG00323.hp2 NA18963.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.290-279G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477281 | |||||||
chr16:66477420 | G | C | 11 | a0001c0001t0004g0002 a0001c0001t0004g0004 a0001c0001t0004g0005 others(8): Show |
15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.290-140G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477420 | |||||||
chr16:66477460 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290-100G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477460 | |||||||
chr16:66477532 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.290-28G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 3/4 | chr16 | 66477532 | |||||||
chr16:66477724 | A | G | 119 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(116): Show |
127 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.440+14A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66477724 | |||||||
chr16:66477810 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.440+100G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66477810 | |||||||
chr16:66478002 | C | T | 2 | a0001c0001t0003g0155 a0001c0007t0003g0245 |
2 | HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.440+292C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478002 | |||||||
chr16:66478158 | C | G | 1 | a0001c0001t0004g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.440+448C>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478158 | |||||||
chr16:66478193 | T | C | 1 | a0001c0001t0009g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.440+483T>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478193 | |||||||
chr16:66478271 | G | A | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.440+561G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478271 | |||||||
chr16:66478385 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.440+675G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478385 | |||||||
chr16:66478387 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.440+677G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478387 | |||||||
chr16:66478443 | A | G | 11 | a0001c0001t0004g0002 a0001c0001t0004g0004 a0001c0001t0004g0005 others(8): Show |
15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.440+733A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478443 | |||||||
chr16:66478589 | G | A | 11 | a0001c0001t0004g0002 a0001c0001t0004g0004 a0001c0001t0004g0005 others(8): Show |
15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.440+879G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478589 | |||||||
chr16:66478801 | G | A | 57 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(54): Show |
59 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.440+1091G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478801 | |||||||
chr16:66478832 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0239 |
2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.440+1122C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478832 | |||||||
chr16:66478906 | G | A | 11 | a0001c0001t0004g0002 a0001c0001t0004g0004 a0001c0001t0004g0005 others(8): Show |
15 | HG00738.hp1 HG01433.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.440+1196G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478906 | |||||||
chr16:66478921 | G | A | 57 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0018 others(54): Show |
63 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.440+1211G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66478921 | |||||||
chr16:66479094 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.440+1384A>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479094 | |||||||
chr16:66479166 | T | G | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441-1420T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479166 | |||||||
chr16:66479168 | G | T | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441-1418G>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479168 | |||||||
chr16:66479169 | C | A | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441-1417C>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479169 | |||||||
chr16:66479207 | A | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.441-1379A>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479207 | |||||||
chr16:66479387 | G | A | 1 | a0001c0001t0012g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441-1199G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479387 | |||||||
chr16:66479601 | G | C | 1 | a0001c0001t0001g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441-985G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479601 | |||||||
chr16:66479675 | T | G | 2 | a0001c0001t0009g0019 a0001c0001t0012g0105 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.441-911T>G | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479675 | |||||||
chr16:66479738 | G | C | 1 | a0001c0001t0003g0150 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.441-848G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479738 | |||||||
chr16:66479799 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.441-787G>C | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479799 | |||||||
chr16:66479942 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0172 |
2 | NA18963.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.441-644C>T | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479942 | |||||||
chr16:66479972 | G | A | 1 | a0001c0001t0006g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.441-614G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66479972 | |||||||
chr16:66480071 | AC | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0204 |
3 | HG02109.hp1 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.441-511delC | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr16 | 66480071 | ||||||
chr16:66480146 | T | A | 9 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(6): Show |
9 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.441-440T>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66480146 | |||||||
chr16:66480205 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.441-381G>A | BEAN1 | ENSG00000166546.15 | transcript | ENST00000536005.7 | protein_coding | 4/4 | chr16 | 66480205 |