Variant report

Variant	rs10066056
Chromosome Location	chr5:107264705-107264706
allele	A/T
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]
rs11745356	0.80[JPT][hapmap]
rs1835978	0.95[JPT][hapmap]
rs6882731	0.84[JPT][hapmap]
rs6886766	0.84[JPT][hapmap]
rs7719708	0.84[JPT][hapmap]
rs7720904	0.84[JPT][hapmap]
rs7722766	0.89[JPT][hapmap]
rs919769	0.89[JPT][hapmap]

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	nsv830440	chr5:107074116-107278905	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv882682	chr5:107213361-107458336	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107261400-107286600	Weak transcription	Aorta	Aorta
2	chr5:107261800-107265800	Weak transcription	Thymus	Thymus
3	chr5:107261800-107273400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr5:107262000-107265600	Weak transcription	Fetal Thymus	thymus
5	chr5:107262400-107265800	Weak transcription	Dnd41	blood
6	chr5:107262400-107267800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:107262400-107268800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:107263000-107272400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr5:107263200-107267400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:107264400-107265800	Enhancers	Primary T cells from cord blood	blood

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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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