Variant report

Variant	rs12062536
Chromosome Location	chr1:216912267-216912268
allele	C/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]
rs11572652	1.00[AMR][1000 genomes]
rs12092631	0.90[AFR][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	nsv508694	chr1:216901014-216923883	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216897400-216958600	Weak transcription	Pancreas	Pancrea
2	chr1:216905200-216913200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:216907400-216913400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr1:216911200-216912400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr1:216911600-216934200	Weak transcription	Psoas Muscle	Psoas
6	chr1:216911800-216913000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr1:216911800-216913000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr1:216912000-216913000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:216912200-216912400	Enhancers	H1 Cell Line	embryonic stem cell
10	chr1:216912200-216912800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr1:216912200-216913000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:216912200-216914400	Enhancers	ES-UCSF4 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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