Variant report

Variant	rs536608728
Chromosome Location	chr8:62035766-62035767
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948922	chr8:61818964-62475097	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	esv3433061	chr8:62034648-62036946	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3479321	chr8:62035225-62035997	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3528976	chr8:62035258-62036022	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3528977	chr8:62035264-62035981	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3528973	chr8:62035274-62035929	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3479324	chr8:62035276-62035969	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3479323	chr8:62035281-62035963	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3479322	chr8:62035294-62035915	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3528975	chr8:62035302-62035949	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv1003680	chr8:62035336-62035865	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv824660	chr8:62035336-62035865	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv824661	chr8:62035336-62035913	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3479325	chr8:62035361-62035893	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv3528978	chr8:62035361-62035893	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
16	esv2761428	chr8:62035527-62045992	Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62034000-62037000	Enhancers	GM12878-XiMat	blood
2	chr8:62034400-62051400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:62035000-62036200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:62035200-62036200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:62035400-62036400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr8:62035600-62036000	Weak transcription	hESC Derived CD56+ Ectoderm 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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