Variant report

Variant	rs7338130
Chromosome Location	chr13:96306146-96306147
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs9561925	0.80[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900934	chr13:96255706-96327574	Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96305800-96306400	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr13:96305800-96306400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:96305800-96306400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr13:96305800-96306400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr13:96306000-96306400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr13:96306000-96306400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr13:96306000-96306400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr13:96306000-96306400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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