Variant report

Variant	rs686556
Chromosome Location	chr6:80939779-80939780
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:80935860..80938788-chr6:80939449..80942433,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10943698	0.82[ASN][1000 genomes]
rs12209624	0.81[ASN][1000 genomes]
rs1535825	0.84[ASN][1000 genomes]
rs1575541	0.80[ASN][1000 genomes]
rs3805911	0.82[ASN][1000 genomes]
rs3805913	0.81[ASN][1000 genomes]
rs3828753	0.81[ASN][1000 genomes]
rs583426	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs590641	0.81[ASN][1000 genomes]
rs643987	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs682482	0.83[ASN][1000 genomes]
rs688867	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs742833	0.81[ASN][1000 genomes]
rs7745301	0.81[ASN][1000 genomes]
rs7746917	0.80[ASN][1000 genomes]
rs7770383	0.82[ASN][1000 genomes]
rs806783	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9294172	0.81[ASN][1000 genomes]
rs9341808	0.83[ASN][1000 genomes]
rs9448911	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830708	chr6:80844283-80996876	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1034096	chr6:80856135-81150170	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv886309	chr6:80880138-80959885	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv886310	chr6:80880138-81025879	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv932996	chr6:80880896-81134991	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv497995	chr6:80883701-81134991	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv1033452	chr6:80888667-81000213	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80896400-80943800	Weak transcription	Right Ventricle	heart
2	chr6:80909000-80940200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr6:80914600-80980400	Weak transcription	Ovary	ovary
4	chr6:80915400-80942000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:80915800-80956000	Weak transcription	Brain Substantia Nigra	brain
6	chr6:80920800-80943600	Weak transcription	Psoas Muscle	Psoas
7	chr6:80920800-80953800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr6:80921200-80940200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr6:80921200-80940200	Weak transcription	HSMMtube	muscle
10	chr6:80921400-80973200	Weak transcription	Primary B cells from cord blood	blood
11	chr6:80922200-80964200	Weak transcription	Fetal Intestine Small	intestine
12	chr6:80924000-80942800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:80924000-80968400	Weak transcription	Gastric	stomach
14	chr6:80924000-80976000	Weak transcription	HSMM	muscle
15	chr6:80927800-80959800	Weak transcription	Aorta	Aorta
16	chr6:80929400-80969200	Weak transcription	Left Ventricle	heart
17	chr6:80932800-80956200	Weak transcription	Lung	lung
18	chr6:80933600-80943800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr6:80935000-80943600	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr6:80936600-80943600	Weak transcription	Pancreas	Pancrea
21	chr6:80936800-80943800	Weak transcription	Fetal Muscle Trunk	muscle
22	chr6:80938000-80956800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr6:80938200-80942000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:80938600-80952800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:80939000-80974800	Weak transcription	Primary T cells from cord blood	blood
26	chr6:80939200-80959600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:80939400-80940200	Weak transcription	Liver	Liver

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