Variant report

Variant	rs36007381
Chromosome Location	chr5:113012877-113012878
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:2)

rs_ID	r²[population]
rs13190018	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34077922	0.83[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv599407	chr5:112981528-113029914	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113011200-113013000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr5:113011200-113013200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr5:113011200-113014200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr5:113011200-113015000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:113011400-113014200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:113011400-113014400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:113011400-113014800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:113012600-113018400	Weak transcription	iPS DF 6.9 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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