Variant report

Variant	rs6701695
Chromosome Location	chr1:175418021-175418022
allele	C/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:15)

rs_ID	r²[population]
rs1385542	0.81[AFR][1000 genomes]
rs2097462	0.97[ASN][1000 genomes]
rs4652090	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4652092	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6677247	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6697736	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6698243	0.88[ASN][1000 genomes]
rs743904	0.94[ASN][1000 genomes]
rs7514113	0.97[ASN][1000 genomes]
rs859462	0.99[ASN][1000 genomes]
rs859474	0.88[ASN][1000 genomes]
rs859475	0.88[ASN][1000 genomes]
rs859476	0.88[ASN][1000 genomes]
rs859479	0.88[ASN][1000 genomes]
rs860907	0.99[ASN][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	esv2764232	chr1:175387997-175504394	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv1792278	chr1:175404515-175429913	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175416400-175418200	Weak transcription	Fetal Brain Male	brain
2	chr1:175417800-175418400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr1:175417800-175419400	Enhancers	GM12878-XiMat	blood
4	chr1:175418000-175418600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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