Variant report

Variant	rs9946894
Chromosome Location	chr18:25233295-25233296
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10469042	1.00[EUR][1000 genomes]
rs1420963	1.00[EUR][1000 genomes]
rs28415309	1.00[EUR][1000 genomes]
rs56774619	0.89[ASN][1000 genomes]
rs59993739	0.89[ASN][1000 genomes]
rs61020210	0.89[ASN][1000 genomes]
rs73396752	0.89[ASN][1000 genomes]
rs73396756	0.89[ASN][1000 genomes]
rs73396787	0.89[ASN][1000 genomes]
rs73944972	0.92[EUR][1000 genomes]
rs73944973	0.89[ASN][1000 genomes]
rs73944977	1.00[EUR][1000 genomes]
rs949196	0.87[EUR][1000 genomes]
rs949197	0.83[EUR][1000 genomes]
rs9946780	1.00[EUR][1000 genomes]
rs9949461	1.00[EUR][1000 genomes]
rs9966333	1.00[EUR][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	esv2761996	chr18:24866083-25818618	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv1061993	chr18:25211720-25239455	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1067348	chr18:25213808-25239455	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv833604	chr18:25226727-25417423	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:25232200-25236000	Weak transcription	Fetal Lung	lung
2	chr18:25233000-25235200	Enhancers	Fetal Heart	heart
3	chr18:25233000-25236000	Weak transcription	HSMMtube	muscle
4	chr18:25233000-25236200	Weak transcription	NH-A	brain
5	chr18:25233200-25240400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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