Variant report

Variant	rs4946443
Chromosome Location	chr6:120139903-120139904
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs13200280	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34290353	0.87[EUR][1000 genomes]
rs6569088	0.84[EUR][1000 genomes]
rs6922103	0.85[EUR][1000 genomes]
rs7739068	0.85[EUR][1000 genomes]
rs7747886	0.84[EUR][1000 genomes]
rs7755856	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7771532	0.84[EUR][1000 genomes]
rs9374826	0.85[EUR][1000 genomes]
rs9374832	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9387678	0.84[EUR][1000 genomes]
rs9387679	0.84[EUR][1000 genomes]
rs9398527	0.85[EUR][1000 genomes]
rs9489811	0.82[EUR][1000 genomes];0.99[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	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:120138800-120140200	Enhancers	Fetal Intestine Large	intestine
2	chr6:120139600-120140200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr6:120139800-120140600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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