Variant report

Variant	rs368208109
Chromosome Location	chr7:150996899-150996900
allele	-/AT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023436	chr7:150967147-150997692	Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
2	esv3524170	chr7:150996609-150997091	Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3478332	chr7:150996620-150997149	Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3478333	chr7:150996620-150997149	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv3360308	chr7:150996625-150997092	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3524171	chr7:150996729-150997146	Bivalent/Poised TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150994000-151000400	Weak transcription	Right Atrium	heart
2	chr7:150996600-150997000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:150996600-150997000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:150996600-150997000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
5	chr7:150996600-150997000	Enhancers	Gastric	stomach
6	chr7:150996600-150997200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:150996600-150997200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:150996600-150997200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
9	chr7:150996600-150997200	ZNF genes & repeats	Fetal Kidney	kidney
10	chr7:150996600-150997200	Bivalent/Poised TSS	Fetal Lung	lung
11	chr7:150996600-150997400	ZNF genes & repeats	Pancreas	Pancrea
12	chr7:150996800-150997000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
13	chr7:150996800-150997200	Bivalent Enhancer	Fetal Brain Male	brain

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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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