Variant report

Variant	rs7634106
Chromosome Location	chr3:23813444-23813445
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs35663853	1.00[EUR][1000 genomes]
rs55867849	1.00[EUR][1000 genomes]
rs56283624	1.00[EUR][1000 genomes]
rs60283861	1.00[EUR][1000 genomes]
rs60740455	1.00[EUR][1000 genomes]
rs61652123	1.00[EUR][1000 genomes]
rs73148287	1.00[EUR][1000 genomes]
rs73148289	1.00[EUR][1000 genomes]
rs73150213	1.00[EUR][1000 genomes]
rs73150216	1.00[EUR][1000 genomes]
rs73150220	1.00[EUR][1000 genomes]
rs73150243	1.00[EUR][1000 genomes]
rs73150260	1.00[EUR][1000 genomes]
rs9883672	1.00[EUR][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	nsv533980	chr3:23445901-24311972	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv834637	chr3:23703928-23886144	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr3:23803400-23836800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:23813400-23816800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte 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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