Variant report

Variant	rs4692111
Chromosome Location	chr4:31034633-31034634
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10084945	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10939328	1.00[YRI][hapmap]
rs2036245	1.00[YRI][hapmap]
rs28532843	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4524343	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4577529	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4615136	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4621393	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4692110	0.83[EUR][1000 genomes]
rs6448736	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6448737	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6448738	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6448740	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6811512	1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6821627	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6824760	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6825405	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6836089	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6836516	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6843199	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6843328	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6844794	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6848676	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6852025	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7657737	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7678773	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9990809	1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.84[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	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr4:31032800-31036400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr4:31033000-31042400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr4:31033200-31036000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:31033200-31036200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr4:31033200-31036200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr4:31033600-31036000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr4:31034200-31036200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:31034200-31043000	Weak transcription	H1 Cell Line	embryonic stem cell

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