Variant report

Variant	rs35391935
Chromosome Location	chr12:86523282-86523283
allele	-/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2761759	chr12:86415936-86747726	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv518059	chr12:86416212-86747726	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041397	chr12:86438607-86737558	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv470311	chr12:86484366-86550783	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3442004	chr12:86514695-86599965	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv2604566	chr12:86522207-86523968	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv2753278	chr12:86522507-86555154	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3492368	chr12:86523201-86523807	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3490430	chr12:86523209-86523742	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3492372	chr12:86523224-86523721	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv5822	chr12:86523228-86523886	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3492370	chr12:86523238-86523701	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3395	chr12:86523239-86523701	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3490385	chr12:86523248-86523707	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv3492373	chr12:86523250-86523691	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3490397	chr12:86523259-86523663	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
18	esv3492369	chr12:86523263-86523691	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
19	esv3490419	chr12:86523266-86523729	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86522600-86523400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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