Variant report

Variant	rs149286832
Chromosome Location	chr5:16124797-16124798
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830217	chr5:16004704-16225229	Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3494749	chr5:16124102-16126500	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	inside rSNPs	n/a
3	esv3468868	chr5:16124662-16125601	Strong transcription Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	n/a
4	esv3428323	chr5:16124683-16125574	Strong transcription Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	n/a
5	esv3494746	chr5:16124705-16125602	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	inside rSNPs	n/a
6	esv3468867	chr5:16124720-16125574	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	n/a
7	esv3494747	chr5:16124728-16125534	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	n/a
8	esv3468866	chr5:16124734-16125534	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	n/a
9	esv3494748	chr5:16124740-16125541	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	n/a
10	nsv471738	chr5:16124796-16125501	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16123400-16124800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:16123400-16125400	Weak transcription	Fetal Heart	heart

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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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