Variant report

Variant	rs10209137
Chromosome Location	chr2:56677613-56677614
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834093	chr2:56538097-56708677	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1004449	chr2:56538460-56715861	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv874171	chr2:56545845-56727178	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv874172	chr2:56638856-56811749	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2757800	chr2:56659685-56851198	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv2759052	chr2:56659685-56851198	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv963150	chr2:56677451-56682246	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56674400-56678200	Enhancers	Fetal Intestine Large	intestine
2	chr2:56675000-56677800	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr2:56675000-56677800	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:56675200-56678000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:56675400-56678200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr2:56675400-56679200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:56676000-56682800	Weak transcription	Pancreas	Pancrea
8	chr2:56676600-56677800	Enhancers	Fetal Kidney	kidney
9	chr2:56676800-56677800	Enhancers	Fetal Intestine Small	intestine
10	chr2:56677000-56678000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr2:56677000-56678000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr2:56677000-56678200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:56677000-56678200	Enhancers	A549	lung
14	chr2:56677200-56678000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr2:56677600-56677800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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