Variant report

Variant	rs182034685
Chromosome Location	chr7:140188058-140188059
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464734	chr7:140108096-140217670	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv608500	chr7:140108096-140217670	Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	esv1803443	chr7:140146694-140263109	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
4	esv3377641	chr7:140181549-140190537	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	esv3492577	chr7:140181601-140190476	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv3492578	chr7:140181601-140190476	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv437576	chr7:140182985-140217670	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	esv3475414	chr7:140187483-140191781	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv1031783	chr7:140187750-140199000	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140179800-140198000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:140180000-140188200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr7:140185400-140192800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr7:140185400-140197000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr7:140185800-140188200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:140185800-140188200	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr7:140185800-140188200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr7:140185800-140188600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:140185800-140198000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr7:140186000-140188400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr7:140186200-140188200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr7:140187800-140188400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:140188000-140188400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:140188000-140188400	Flanking Active TSS	K562	blood
15	chr7:140188000-140188600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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