Variant report

Variant	rs184319835
Chromosome Location	chr19:40122170-40122171
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv579509	chr19:40004640-40133438	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	esv34120	chr19:40044635-40131820	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv579510	chr19:40121448-40123536	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40121800-40122200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr19:40121800-40122200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr19:40121800-40122200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr19:40121800-40122400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr19:40121800-40122600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr19:40122000-40122600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr19:40122000-40123000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr19:40122000-40127600	Weak transcription	Placenta	Placenta

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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