Variant report

Variant	rs58991236
Chromosome Location	chr3:150564226-150564227
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16862868	1.00[EUR][1000 genomes]
rs16862916	1.00[EUR][1000 genomes]
rs56220205	1.00[EUR][1000 genomes]
rs57454586	1.00[EUR][1000 genomes]
rs6777167	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73871604	1.00[EUR][1000 genomes]
rs73871606	1.00[EUR][1000 genomes]
rs73871609	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	nsv532662	chr3:150180747-150633414	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv818177	chr3:150541363-150566422	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150560600-150566400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:150561400-150566000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr3:150563200-150565600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr3:150563200-150566200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:150563200-150566400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr3:150563400-150566200	Weak transcription	HUES64 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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