Variant report

Variant	rs62444595
Chromosome Location	chr7:14414260-14414261
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10247193	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4721317	1.00[ASN][1000 genomes]
rs62444572	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62444579	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62444597	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62444599	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62444600	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62445620	1.00[ASN][1000 genomes]
rs73052171	1.00[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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv606281	chr7:14388381-14443963	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14413600-14415600	Enhancers	H9 Cell Line	embryonic stem cell
2	chr7:14414000-14415600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr7:14414200-14415400	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr7:14414200-14416000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr7:14414200-14416800	Enhancers	HUES64 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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