Variant report

Variant	rs4389916
Chromosome Location	chr8:124594611-124594612
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10092188	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11780880	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12541523	0.88[EUR][1000 genomes]
rs13256806	0.88[EUR][1000 genomes]
rs13260517	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13262816	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13265242	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4006406	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4382457	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4870856	0.95[EUR][1000 genomes]
rs6470157	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7010236	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7816943	0.93[EUR][1000 genomes]
rs7840558	0.88[EUR][1000 genomes]
rs7843874	0.95[EUR][1000 genomes]
rs9642867	0.95[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831450	chr8:124471741-124661359	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124575600-124598600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:124590800-124597000	Weak transcription	HSMMtube	muscle
3	chr8:124592800-124596200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:124593000-124595800	Weak transcription	HMEC	breast
5	chr8:124594000-124597000	Weak transcription	Fetal Heart	heart

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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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