Variant report

Variant	rs143410311
Chromosome Location	chr7:119235244-119235245
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	nsv889100	chr7:118744450-119247571	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv949327	chr7:119179990-119402882	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv889114	chr7:119206096-119440159	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv3478059	chr7:119228052-119236067	Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3478060	chr7:119228068-119236064	Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
6	esv11548	chr7:119232822-119236164	Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv1020551	chr7:119232910-119292763	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
8	nsv981410	chr7:119233323-119236164	Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
9	nsv970422	chr7:119233323-119244802	Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119233800-119235800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr7:119234000-119235600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr7:119234000-119235600	Enhancers	H1 Cell Line	embryonic stem cell
4	chr7:119234000-119236400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr7:119234200-119235600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr7:119234600-119235600	Enhancers	H9 Cell Line	embryonic stem cell
7	chr7:119234600-119235800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:119234600-119235800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:119234600-119235800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr7:119234600-119236200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr7:119234800-119236400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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