Variant report

Variant	rs7814093
Chromosome Location	chr8:124595483-124595484
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10105316	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17253999	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2385455	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2385456	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs28445658	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs28484830	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs28490211	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28613586	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28825116	0.86[ASN][1000 genomes]
rs35066700	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4871390	0.87[ASN][1000 genomes]
rs4871392	0.88[ASN][1000 genomes]
rs4871394	0.83[ASN][1000 genomes]
rs55987314	0.97[ASN][1000 genomes]
rs62520905	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs72711208	0.93[ASN][1000 genomes]
rs72711214	0.80[AMR][1000 genomes];0.92[ASN][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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