Variant report

Variant	rs184234250
Chromosome Location	chr9:96116684-96116685
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv893582	chr9:95963114-96116937	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv893584	chr9:96002983-96116937	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv1798245	chr9:96098930-96120432	Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2761278	chr9:96115678-96126104	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96109200-96127800	Weak transcription	Right Atrium	heart
2	chr9:96111200-96122400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:96115400-96117200	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
4	chr9:96115600-96117000	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
5	chr9:96115600-96117200	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
6	chr9:96115600-96117200	Genic enhancers	H1 Cell Line	embryonic stem cell
7	chr9:96115800-96117000	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr9:96115800-96117400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr9:96116000-96117000	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr9:96116000-96117400	Genic enhancers	H9 Cell Line	embryonic stem cell
11	chr9:96116000-96118000	Genic enhancers	HUES64 Cell Line	embryonic stem cell
12	chr9:96116000-96120200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr9:96116200-96119000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr9:96116200-96119800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:96116600-96117000	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
16	chr9:96116600-96117000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr9:96116600-96117200	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
18	chr9:96116600-96117800	Weak transcription	Placenta	Placenta

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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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