Variant report

Variant	rs4856414
Chromosome Location	chr3:82734786-82734787
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs17019965	0.81[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs17019967	0.89[ASN][1000 genomes]
rs6783313	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013820	chr3:82175705-82968181	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv834750	chr3:82645025-82802783	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv460734	chr3:82707769-82766788	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
4	nsv590781	chr3:82707769-82766788	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
5	nsv1010803	chr3:82708244-82766788	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
6	nsv1008386	chr3:82712103-82768690	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
7	nsv590782	chr3:82715343-82766788	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
8	nsv1005871	chr3:82719273-82767152	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
9	nsv536607	chr3:82719273-82767152	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
10	nsv877045	chr3:82728631-82808608	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:82731600-82737200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr3:82734600-82735800	Enhancers	NH-A	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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