Variant report

Variant	rs6795777
Chromosome Location	chr3:68790218-68790219
allele	G/T
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]
rs11128087	0.82[EUR][1000 genomes]
rs1504297	0.82[EUR][1000 genomes]
rs1602195	0.91[EUR][1000 genomes]
rs2313851	0.82[EUR][1000 genomes]
rs34720222	0.87[ASN][1000 genomes]
rs4855498	0.82[EUR][1000 genomes]
rs4855499	0.82[EUR][1000 genomes]
rs6549141	0.86[EUR][1000 genomes]
rs6549143	0.92[CEU][hapmap]
rs6775453	0.86[EUR][1000 genomes]
rs6796615	0.89[EUR][1000 genomes]
rs867310	0.85[EUR][1000 genomes]
rs9681520	0.85[EUR][1000 genomes]
rs971382	0.82[EUR][1000 genomes]
rs9836496	0.84[EUR][1000 genomes]
rs9841811	0.85[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	nsv834722	chr3:68775036-68974120	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68789400-68801200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:68789800-68790600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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

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