Variant report

Variant	rs1170635
Chromosome Location	chr2:124968659-124968660
allele	C/G
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:12)

rs_ID	r²[population]
rs10173293	0.98[ASN][1000 genomes]
rs1170618	0.96[ASN][1000 genomes]
rs12711674	0.99[ASN][1000 genomes]
rs12711676	0.98[ASN][1000 genomes]
rs13395031	0.98[ASN][1000 genomes]
rs2901199	0.98[ASN][1000 genomes]
rs34213745	0.99[ASN][1000 genomes]
rs6541944	1.00[ASN][1000 genomes]
rs6707012	1.00[ASN][1000 genomes]
rs6719774	0.97[ASN][1000 genomes]
rs779986	0.94[ASN][1000 genomes]
rs779989	0.94[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	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv874989	chr2:124892592-125176030	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:124968400-124971400	Weak transcription	ES-I3 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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