Variant report

Variant	rs39330
Chromosome Location	chr7:103449555-103449556
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs262338	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	nsv427799	chr7:103250733-103454202	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103446200-103452000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr7:103449200-103451000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr7:103449200-103451200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr7:103449200-103451200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr7:103449200-103451200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr7:103449200-103451200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:103449400-103450200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:103449400-103450200	Genic enhancers	HepG2	liver
9	chr7:103449400-103450200	Enhancers	K562	blood
10	chr7:103449400-103450400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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

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