Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1615441	0.83[YRI][hapmap]
rs1618774	0.83[YRI][hapmap]
rs1678719	0.82[YRI][hapmap]
rs1678720	0.82[YRI][hapmap]
rs1678721	0.83[YRI][hapmap]
rs1678722	0.83[YRI][hapmap]
rs1678724	0.83[YRI][hapmap]
rs1678728	0.82[YRI][hapmap]
rs1678729	0.82[YRI][hapmap]
rs1678737	0.82[YRI][hapmap]
rs1678741	0.83[YRI][hapmap]
rs1678743	0.96[YRI][hapmap];0.90[AFR][1000 genomes]
rs1678744	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1678745	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1678746	0.84[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1678747	1.00[EUR][1000 genomes]
rs1738185	1.00[EUR][1000 genomes]
rs1738186	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1738188	0.95[YRI][hapmap];0.90[AFR][1000 genomes]
rs1738191	0.87[YRI][hapmap]
rs1738193	0.83[YRI][hapmap]
rs1738194	0.83[YRI][hapmap]
rs1738200	0.83[YRI][hapmap]
rs1738206	0.83[YRI][hapmap]
rs1738207	0.83[YRI][hapmap]
rs1738209	0.83[YRI][hapmap]
rs55675276	1.00[EUR][1000 genomes]
rs7772516	1.00[EUR][1000 genomes]
rs7774152	1.00[EUR][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	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv830643	chr6:38726675-38905589	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38766800-38824400	Weak transcription	K562	blood
2	chr6:38804600-38821000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:38812600-38821000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:38816800-38818200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:38817200-38818200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:38817200-38818800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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