Variant report

Variant	rs4755139
Chromosome Location	chr11:106062504-106062505
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10450645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10750740	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs17105468	1.00[EUR][1000 genomes]
rs17105525	1.00[EUR][1000 genomes]
rs1940757	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1940762	0.87[AMR][1000 genomes]
rs1940768	0.87[AMR][1000 genomes]
rs1940784	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1944771	0.86[AFR][1000 genomes]
rs1955019	0.85[AFR][1000 genomes]
rs2096832	0.87[AFR][1000 genomes]
rs4332487	1.00[EUR][1000 genomes]
rs4427534	1.00[EUR][1000 genomes]
rs4531437	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4754145	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs494766	1.00[EUR][1000 genomes]
rs497271	1.00[EUR][1000 genomes]
rs501777	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs501889	1.00[EUR][1000 genomes]
rs516531	1.00[EUR][1000 genomes]
rs527993	1.00[EUR][1000 genomes]
rs529861	1.00[EUR][1000 genomes]
rs535189	1.00[EUR][1000 genomes]
rs579770	1.00[EUR][1000 genomes]
rs58379581	1.00[EUR][1000 genomes]
rs586279	1.00[EUR][1000 genomes]
rs601181	1.00[EUR][1000 genomes]
rs606871	1.00[CHD][hapmap];0.81[GIH][hapmap];0.86[JPT][hapmap];1.00[EUR][1000 genomes]
rs629793	1.00[EUR][1000 genomes]
rs645748	1.00[EUR][1000 genomes]
rs646242	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs660564	1.00[CHD][hapmap];0.81[GIH][hapmap];0.86[JPT][hapmap];1.00[EUR][1000 genomes]
rs661099	1.00[EUR][1000 genomes]
rs664549	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs669266	1.00[EUR][1000 genomes]
rs671671	0.86[JPT][hapmap];1.00[EUR][1000 genomes]
rs682320	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7481097	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048381	chr11:105945117-106561574	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv898358	chr11:105999580-106182251	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv430428	chr11:106005901-106173046	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1036986	chr11:106046850-106075023	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106045800-106063600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:106057400-106071800	Weak transcription	Pancreas	Pancrea
3	chr11:106062000-106062600	Enhancers	Fetal Brain Male	brain

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