Variant report

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10001112	1.00[EUR][1000 genomes]
rs10005772	0.90[AFR][1000 genomes]
rs10012964	1.00[EUR][1000 genomes]
rs11930802	1.00[EUR][1000 genomes]
rs11934590	1.00[EUR][1000 genomes]
rs11947636	0.95[AFR][1000 genomes]
rs1444955	1.00[EUR][1000 genomes]
rs1495144	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17008641	1.00[EUR][1000 genomes]
rs1994956	1.00[EUR][1000 genomes]
rs2119793	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28431455	1.00[EUR][1000 genomes]
rs28523312	1.00[EUR][1000 genomes]
rs28558705	0.90[AFR][1000 genomes]
rs28656956	0.87[AFR][1000 genomes]
rs28727985	0.85[AMR][1000 genomes]
rs28894761	0.89[AFR][1000 genomes]
rs437295	1.00[EUR][1000 genomes]
rs438500	1.00[EUR][1000 genomes]
rs57866246	1.00[EUR][1000 genomes]
rs60097326	0.84[AFR][1000 genomes]
rs6825565	1.00[EUR][1000 genomes]
rs6826424	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6828383	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6831720	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6843960	0.95[AFR][1000 genomes]
rs72955273	1.00[EUR][1000 genomes]
rs72955986	1.00[AMR][1000 genomes]
rs72955991	1.00[AMR][1000 genomes]
rs7668554	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7668852	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7688976	0.92[AFR][1000 genomes]
rs7691569	1.00[EUR][1000 genomes]
rs9990978	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9993950	0.81[AFR][1000 genomes]
rs9999113	0.90[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	nsv879514	chr4:85057124-85272572	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv829997	chr4:85244076-85409405	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85259800-85263200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:85259800-85263400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:85260200-85263000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:85260400-85261800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:85260800-85261000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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