Variant report

Variant	rs11685113
Chromosome Location	chr2:56177013-56177014
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1432561	0.92[CHB][hapmap];0.85[CHD][hapmap]
rs4258837	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4672080	0.90[CHB][hapmap]
rs4672081	0.80[EUR][1000 genomes]
rs4672082	0.80[EUR][1000 genomes]
rs6704991	0.92[CHB][hapmap];0.85[CHD][hapmap]
rs7564964	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531374	chr2:55653723-56299784	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv874161	chr2:56154316-56203798	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11685113	ASB3	cis	parietal	SCAN

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56171000-56185000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:56175600-56181400	Weak transcription	HUVEC	blood vessel
3	chr2:56176000-56181400	Weak transcription	Adipose Nuclei	Adipose
4	chr2:56176400-56177200	Enhancers	NHEK	skin
5	chr2:56176400-56177400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:56176400-56181000	Weak transcription	Osteobl	bone
7	chr2:56176400-56181400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:56176600-56181200	Weak transcription	Fetal Kidney	kidney
9	chr2:56176800-56177800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:56177000-56181400	Weak transcription	Hela-S3	cervix

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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