Variant report

Variant	rs73372745
Chromosome Location	chr14:84910405-84910406
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11846527	0.86[EUR][1000 genomes]
rs17120012	0.83[AMR][1000 genomes]
rs73375642	1.00[EUR][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	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr14:84904000-84912600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr14:84909200-84910600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:84909200-84912600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr14:84909400-84910800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr14:84909600-84910800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr14:84909600-84911000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:84909600-84912600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr14:84910200-84911000	Enhancers	iPS-15b 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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