Variant report

Variant	rs184176469
Chromosome Location	chr13:62659760-62659761
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761266	chr13:61928642-62690828	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv948810	chr13:62003256-62968196	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv900252	chr13:62502166-62687843	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv900253	chr13:62515266-62660299	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv900254	chr13:62549703-62660299	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv900255	chr13:62549703-62680229	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv900256	chr13:62569634-62660299	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv832630	chr13:62651865-62811428	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv561879	chr13:62655236-62666114	Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
10	nsv561883	chr13:62655365-62660299	Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
11	nsv561884	chr13:62655365-62666114	Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
12	nsv561891	chr13:62656074-62660299	Enhancers	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	chr13:62659400-62660200	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr13:62659400-62660400	Enhancers	H1 Cell Line	embryonic stem cell
3	chr13:62659400-62660400	Enhancers	H9 Cell Line	embryonic stem cell
4	chr13:62659400-62660400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr13:62659400-62660400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr13:62659400-62660400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr13:62659400-62660400	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr13:62659600-62660200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr13:62659600-62660400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr13:62659600-62660400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:62659600-62660400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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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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