Variant report

Variant	rs201097364
Chromosome Location	chr7:126297268-126297269
allele	-/A
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	nsv529300	chr7:125669493-126587858	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1032938	chr7:126067684-126587859	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv539119	chr7:126067684-126587859	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv889187	chr7:126219766-126478190	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv1032108	chr7:126278349-126362592	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	nsv5939	chr7:126279355-126322778	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	esv2158688	chr7:126297058-126297481	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3521605	chr7:126297128-126297409	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3521608	chr7:126297134-126297354	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3521606	chr7:126297153-126297331	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3442117	chr7:126297173-126297301	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3521609	chr7:126297180-126297379	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3521610	chr7:126297199-126297339	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv1009957	chr7:126297211-126297280	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv1733605	chr7:126297268-126297338	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126296400-126299400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr7:126296800-126299200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:126297000-126298000	Enhancers	GM12878-XiMat	blood
4	chr7:126297000-126301600	Weak transcription	ES-I3 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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