Variant report

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:103253081..103256166-chr7:103404446..103406601,3	K562	blood:
2	chr7:103239547..103241356-chr7:103252874..103254925,2	K562	blood:
3	chr7:103253053..103254863-chr7:103298954..103300587,2	K562	blood:
4	chr7:103246004..103248480-chr7:103252679..103255017,2	K562	blood:
5	chr7:103253050..103254714-chr7:103265200..103267338,2	MCF-7	breast:
6	chr7:103253287..103254849-chr7:103287404..103290090,2	K562	blood:
7	chr7:103253816..103255808-chr7:103257490..103259015,2	K562	blood:

No data

rSNPs within LD-proxies of this variant (count:25)

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]
rs2535775	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2535776	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2535779	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[AFR][1000 genomes];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]
rs2711872	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[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs362657	1.00[EUR][1000 genomes]
rs362751	1.00[EUR][1000 genomes]
rs362775	1.00[EUR][1000 genomes]
rs57665391	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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
3	nsv427799	chr7:103250733-103454202	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 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	chr7:103245000-103259600	Weak transcription	HepG2	liver
2	chr7:103253600-103255400	Enhancers	Fetal Heart	heart
3	chr7:103254000-103254400	Enhancers	Left Ventricle	heart
4	chr7:103254000-103255000	Enhancers	K562	blood

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