Variant report

Variant	rs605994
Chromosome Location	chr9:13655747-13655748
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023684	chr9:13529680-13744602	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv540067	chr9:13529680-13744602	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv892587	chr9:13601074-13732363	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv1843958	chr9:13631992-13706651	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2547786	chr9:13655005-13656498	Weak transcription	n/a	n/a	inside rSNPs	n/a
6	esv1973014	chr9:13655222-13655950	Weak transcription	n/a	n/a	inside rSNPs	n/a
7	esv3481970	chr9:13655306-13655835	Weak transcription	n/a	n/a	inside rSNPs	n/a
8	esv3501771	chr9:13655319-13655848	Weak transcription	n/a	n/a	inside rSNPs	n/a
9	esv3501772	chr9:13655319-13655848	Weak transcription	n/a	n/a	inside rSNPs	n/a
10	esv3429936	chr9:13655330-13655835	Weak transcription	n/a	n/a	inside rSNPs	n/a
11	esv3481971	chr9:13655337-13655809	Weak transcription	n/a	n/a	inside rSNPs	n/a
12	esv3481968	chr9:13655339-13655775	Weak transcription	n/a	n/a	inside rSNPs	n/a
13	esv3481969	chr9:13655356-13655766	Weak transcription	n/a	n/a	inside rSNPs	n/a
14	esv3481972	chr9:13655398-13655748	Weak transcription	n/a	n/a	inside rSNPs	n/a
15	esv3481973	chr9:13655412-13655755	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13651600-13660800	Weak transcription	Right Atrium	heart

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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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