Variant report

Variant	rs371404978
Chromosome Location	chr11:109021580-109021581
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv1040650	chr11:108859584-109174553	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv3322405	chr11:109020592-109021690	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:109021000-109021600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr11:109021200-109021600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:109021200-109021600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr11:109021200-109021600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr11:109021400-109021600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr11:109021400-109021600	Enhancers	Aorta	Aorta
7	chr11:109021400-109021800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr11:109021400-109022200	Weak transcription	ES-UCSF4 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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