Variant report

Variant	rs7817305
Chromosome Location	chr8:51224953-51224954
allele	C/T
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	nsv916392	chr8:50827638-51395140	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv948436	chr8:51115028-51917504	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv470212	chr8:51176635-51227506	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv6185	chr8:51213648-51237196	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3420535	chr8:51223299-51227997	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2437712	chr8:51224383-51229129	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv5640	chr8:51224773-51228586	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv2077062	chr8:51224808-51228484	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3479195	chr8:51224847-51228421	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv2593415	chr8:51224848-51228925	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv824625	chr8:51224877-51228347	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3479196	chr8:51224901-51228389	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3479193	chr8:51224912-51228348	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv3479192	chr8:51224919-51228339	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv4199	chr8:51224948-51228391	Enhancers	Chromatin interactive region	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	chr8:51223400-51225000	Enhancers	H9 Derived Neuron 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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