Variant report

Variant	rs7756833
Chromosome Location	chr6:38903220-38903221
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:38902804..38905532-chr6:38908040..38910496,2	K562	blood:
2	chr6:38901364..38904102-chr6:38904353..38906720,2	K562	blood:
3	chr6:38902602..38904242-chr6:38904516..38906720,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10305417	1.00[EUR][1000 genomes]
rs10305519	1.00[EUR][1000 genomes]
rs41376545	1.00[EUR][1000 genomes]
rs55643263	1.00[EUR][1000 genomes]
rs55650855	1.00[EUR][1000 genomes]
rs55714548	1.00[EUR][1000 genomes]
rs56113843	1.00[EUR][1000 genomes]
rs57188158	1.00[EUR][1000 genomes]
rs58092834	1.00[EUR][1000 genomes]
rs59648883	1.00[EUR][1000 genomes]
rs60160720	1.00[EUR][1000 genomes]
rs60702678	1.00[EUR][1000 genomes]
rs61232244	1.00[EUR][1000 genomes]
rs73410586	1.00[EUR][1000 genomes]
rs73410602	1.00[EUR][1000 genomes]
rs73412406	1.00[EUR][1000 genomes]
rs73412421	1.00[EUR][1000 genomes]
rs73412424	1.00[EUR][1000 genomes]
rs73412493	1.00[EUR][1000 genomes]
rs73414403	1.00[EUR][1000 genomes]
rs73424127	1.00[EUR][1000 genomes]
rs73426190	1.00[EUR][1000 genomes]
rs73428116	1.00[EUR][1000 genomes]
rs7739218	1.00[EUR][1000 genomes]
rs7772516	1.00[AFR][1000 genomes]
rs7774152	1.00[YRI][hapmap];1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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
3	nsv1028088	chr6:38821047-39163549	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv538205	chr6:38821047-39163549	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv885821	chr6:38843970-39039503	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38901600-38904400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr6:38902800-38903800	Enhancers	Brain Germinal Matrix	brain

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