Variant report

Variant	rs2204609
Chromosome Location	chr4:28107460-28107461
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12501876	0.82[ASN][1000 genomes]
rs12507249	0.93[ASN][1000 genomes]
rs12643515	0.93[ASN][1000 genomes]
rs1405681	0.92[ASN][1000 genomes]
rs6834744	0.99[ASN][1000 genomes]
rs6835345	0.82[ASN][1000 genomes]
rs6850713	0.82[ASN][1000 genomes]
rs7656594	0.92[ASN][1000 genomes]
rs7658870	0.82[ASN][1000 genomes]
rs7658948	0.82[ASN][1000 genomes]
rs7680723	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007066	chr4:28001862-28131764	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1008691	chr4:28051516-28193042	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1008160	chr4:28097388-28116969	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:28106200-28108800	Enhancers	HepG2	liver

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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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