Variant report

Variant	rs58572650
Chromosome Location	chr6:23535586-23535587
allele	A/T
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:2)

rs_ID	r²[population]
rs59595221	1.00[AFR][1000 genomes]
rs60843557	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422291	chr6:23466080-23600459	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1029930	chr6:23481989-24289948	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:23532200-23535800	Enhancers	Muscle Satellite Cultured Cells	--
2	chr6:23533400-23536000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:23533400-23536200	Enhancers	Brain Germinal Matrix	brain
4	chr6:23533800-23535600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:23534200-23537600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:23535000-23535600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr6:23535000-23536000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr6:23535200-23535600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:23535200-23535800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:23535400-23535800	Enhancers	ES-I3 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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