Variant report

Variant	rs7677238
Chromosome Location	chr4:144013964-144013965
allele	G/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]
rs10519682	1.00[AMR][1000 genomes]
rs11944825	1.00[AMR][1000 genomes]
rs11945757	1.00[AMR][1000 genomes]
rs1440409	1.00[AMR][1000 genomes]
rs17017390	1.00[AMR][1000 genomes]
rs17017397	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17017481	1.00[AMR][1000 genomes]
rs17017495	1.00[AMR][1000 genomes]
rs17017555	1.00[AMR][1000 genomes]
rs17017571	1.00[AMR][1000 genomes]
rs4132265	1.00[AMR][1000 genomes]
rs58337819	1.00[AMR][1000 genomes]
rs58547743	1.00[AMR][1000 genomes]
rs61310654	1.00[AMR][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	nsv880176	chr4:143929235-144027729	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1034895	chr4:143945139-144079655	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143998200-144021400	Weak transcription	Ovary	ovary
2	chr4:144013400-144014200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr4:144013600-144014200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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