Variant report

Variant	rs10282835
Chromosome Location	chr8:99408730-99408731
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:99407529..99410363-chr8:99413128..99417283,3	MCF-7	breast:
2	chr8:99405535..99409022-chr8:99413535..99417090,3	MCF-7	breast:
3	chr8:99404229..99407822-chr8:99408436..99411402,4	MCF-7	breast:
4	chr8:99402942..99405077-chr8:99407584..99409359,2	K562	blood:
5	chr8:99407982..99409510-chr8:99409627..99412103,2	MCF-7	breast:
6	chr8:99405199..99406965-chr8:99408440..99410954,3	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11785588	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12386830	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13277523	1.00[ASN][1000 genomes]
rs13282021	1.00[CHB][hapmap]
rs16896995	1.00[ASN][1000 genomes]
rs16897028	1.00[ASN][1000 genomes]
rs16897050	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs16897058	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs16897069	1.00[ASN][1000 genomes]
rs28621642	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34018826	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4554439	1.00[ASN][1000 genomes]
rs4574821	1.00[ASN][1000 genomes]
rs4615538	1.00[ASN][1000 genomes]
rs55793219	1.00[ASN][1000 genomes]
rs55921088	1.00[ASN][1000 genomes]
rs55947965	1.00[ASN][1000 genomes]
rs56185259	1.00[ASN][1000 genomes]
rs56214625	1.00[ASN][1000 genomes]
rs56246659	1.00[ASN][1000 genomes]
rs6982282	1.00[ASN][1000 genomes]
rs6982285	1.00[ASN][1000 genomes]
rs72666612	1.00[ASN][1000 genomes]
rs72666616	1.00[ASN][1000 genomes]
rs72666618	1.00[ASN][1000 genomes]
rs72666619	1.00[ASN][1000 genomes]
rs72666623	1.00[ASN][1000 genomes]
rs72666624	1.00[ASN][1000 genomes]
rs72666625	1.00[ASN][1000 genomes]
rs72666629	1.00[ASN][1000 genomes]
rs72666633	1.00[ASN][1000 genomes]
rs72666638	1.00[ASN][1000 genomes]
rs72666642	1.00[ASN][1000 genomes]
rs72666643	1.00[ASN][1000 genomes]
rs72666649	1.00[ASN][1000 genomes]
rs72666652	1.00[ASN][1000 genomes]
rs72666655	1.00[ASN][1000 genomes]
rs72666661	1.00[ASN][1000 genomes]
rs72666665	1.00[ASN][1000 genomes]
rs72666666	1.00[ASN][1000 genomes]
rs72666673	1.00[ASN][1000 genomes]
rs73699303	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7835203	1.00[ASN][1000 genomes]
rs7839115	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7842869	1.00[CHB][hapmap];1.00[ASN][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	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv831406	chr8:99290745-99482076	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99395400-99415200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:99395600-99409400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:99396800-99410000	Weak transcription	Fetal Lung	lung
4	chr8:99397000-99411600	Weak transcription	Right Ventricle	heart
5	chr8:99406400-99409800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr8:99406400-99410400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:99406800-99410200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr8:99407600-99410200	Weak transcription	HMEC	breast
9	chr8:99408600-99408800	Enhancers	Esophagus	oesophagus
10	chr8:99408600-99408800	Enhancers	Fetal Muscle Trunk	muscle
11	chr8:99408600-99408800	Enhancers	NHLF	lung
12	chr8:99408600-99409000	Enhancers	Fetal Stomach	stomach
13	chr8:99408600-99409000	Enhancers	Right Atrium	heart
14	chr8:99408600-99409200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:99408600-99410600	Enhancers	NHDF-Ad	bronchial
16	chr8:99408600-99416600	Enhancers	Ovary	ovary

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