Variant report

Variant	rs537342522
Chromosome Location	chr13:93998690-93998691
allele	A/G
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	nsv869070	chr13:93347616-94286933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1053035	chr13:93842576-94229732	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv541880	chr13:93842576-94229732	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv900919	chr13:93957816-94030693	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv530636	chr13:93997311-94281707	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93996400-93999000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:93996600-93998800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr13:93996600-93998800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr13:93996800-93998800	Enhancers	Fetal Brain Female	brain
5	chr13:93997000-93999800	Weak transcription	HepG2	liver
6	chr13:93997200-93998800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr13:93997200-93998800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr13:93997600-93998800	Enhancers	Fetal Intestine Small	intestine
9	chr13:93998000-93998800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:93998200-93999000	Enhancers	Fetal Kidney	kidney
11	chr13:93998400-93998800	Enhancers	Fetal Intestine Large	intestine
12	chr13:93998400-93998800	Enhancers	Fetal Lung	lung
13	chr13:93998600-93998800	Enhancers	Fetal Brain Male	brain
14	chr13:93998600-94000200	ZNF genes & repeats	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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