Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:33354992..33357519-chr7:33360634..33362706,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs17398949	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17786463	0.82[EUR][1000 genomes]
rs2109525	0.94[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs56268815	0.82[EUR][1000 genomes]
rs60418513	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61706828	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73099265	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73101663	0.85[EUR][1000 genomes]
rs73101665	0.85[EUR][1000 genomes]
rs73101668	0.85[EUR][1000 genomes]
rs73101671	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73101690	0.84[EUR][1000 genomes]
rs73101699	0.82[EUR][1000 genomes]
rs73103504	0.81[EUR][1000 genomes]
rs73103508	0.81[EUR][1000 genomes]
rs73103514	0.81[EUR][1000 genomes]
rs73103533	0.82[EUR][1000 genomes]
rs73103557	0.81[EUR][1000 genomes]
rs7779232	0.81[EUR][1000 genomes]
rs7793719	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606610	chr7:33218763-33486316	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1016416	chr7:33241443-33559477	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv916660	chr7:33272493-33506384	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv887925	chr7:33304218-33361323	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33340000-33358600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr7:33343200-33361600	Weak transcription	Brain Angular Gyrus	brain
3	chr7:33344200-33359000	Weak transcription	Spleen	Spleen
4	chr7:33354400-33358000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr7:33355200-33419600	Weak transcription	Primary T cells from cord blood	blood
6	chr7:33355400-33357600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr7:33357200-33357600	ZNF genes & repeats	Aorta	Aorta
8	chr7:33357200-33357600	ZNF genes & repeats	Ovary	ovary
9	chr7:33357400-33357800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr7:33357400-33358000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
11	chr7:33357400-33358000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood

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