Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:103220150..103223008-chr7:103223285..103225999,2	K562	blood:
2	chr7:103224194..103227224-chr7:103230117..103233349,3	K562	blood:

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

rs_ID	r²[population]
rs2535756	1.00[EUR][1000 genomes]
rs2535758	1.00[EUR][1000 genomes]
rs2535761	1.00[EUR][1000 genomes]
rs2535767	1.00[EUR][1000 genomes]
rs2535772	1.00[AFR][1000 genomes]
rs2535776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2535779	1.00[EUR][1000 genomes]
rs2535780	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2535782	1.00[EUR][1000 genomes]
rs2711841	1.00[EUR][1000 genomes]
rs2711855	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2711856	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2711857	1.00[EUR][1000 genomes]
rs2711858	1.00[EUR][1000 genomes]
rs2711859	1.00[EUR][1000 genomes]
rs2711866	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2711868	1.00[EUR][1000 genomes]
rs2711871	1.00[AFR][1000 genomes]
rs2711872	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2711880	1.00[EUR][1000 genomes]
rs28396636	1.00[EUR][1000 genomes]
rs28417002	1.00[EUR][1000 genomes]
rs2907932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3109325	1.00[AFR][1000 genomes]
rs362657	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs362751	1.00[EUR][1000 genomes]
rs362775	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	nsv491911	chr7:102967150-103403622	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831085	chr7:103140672-103342388	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103206000-103243400	Weak transcription	K562	blood
2	chr7:103220200-103229000	Weak transcription	HepG2	liver
3	chr7:103224200-103224400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:103224200-103224400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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