Variant report

Variant	rs10098273
Chromosome Location	chr8:102956174-102956175
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:102942428..102944500-chr8:102955135..102957986,2	MCF-7	breast:
2	chr8:102952850..102955242-chr8:102955407..102957253,2	MCF-7	breast:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10099842	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10955277	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1119377	0.90[EUR][1000 genomes]
rs11778653	0.96[EUR][1000 genomes]
rs12545403	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13278642	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1371739	0.91[EUR][1000 genomes]
rs1371740	0.89[EUR][1000 genomes]
rs1543771	0.90[EUR][1000 genomes]
rs17495818	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1866690	0.89[EUR][1000 genomes]
rs1866691	0.90[EUR][1000 genomes]
rs1866692	0.90[EUR][1000 genomes]
rs1866693	0.90[EUR][1000 genomes]
rs4145554	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4734042	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs4734043	0.90[EUR][1000 genomes]
rs4734044	0.90[EUR][1000 genomes]
rs4734045	0.90[EUR][1000 genomes]
rs4734046	0.90[EUR][1000 genomes]
rs4734047	0.90[EUR][1000 genomes]
rs4734048	0.90[EUR][1000 genomes]
rs4734602	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4734603	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4734604	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4734606	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6468803	0.96[EUR][1000 genomes]
rs6468804	0.89[EUR][1000 genomes]
rs6468805	0.90[EUR][1000 genomes]
rs6468806	0.90[EUR][1000 genomes]
rs6468807	0.90[EUR][1000 genomes]
rs6981347	0.82[EUR][1000 genomes]
rs6982001	0.85[EUR][1000 genomes]
rs6991019	0.93[EUR][1000 genomes]
rs6991178	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6995105	0.89[EUR][1000 genomes]
rs6999047	0.90[EUR][1000 genomes]
rs6999316	0.91[EUR][1000 genomes]
rs7003320	0.81[EUR][1000 genomes]
rs7010848	0.95[EUR][1000 genomes]
rs7015981	0.93[EUR][1000 genomes]
rs7820244	0.91[EUR][1000 genomes]
rs7823856	0.91[EUR][1000 genomes]
rs7838556	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7838767	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7839884	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7840045	0.89[EUR][1000 genomes]
rs7841927	0.90[EUR][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	nsv1018653	chr8:102818271-103009082	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv539700	chr8:102818271-103009082	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv831411	chr8:102937991-103108140	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102920600-102956600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr8:102944400-102964000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr8:102948600-102962600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:102951000-102961400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:102953600-102964800	Weak transcription	Ovary	ovary
6	chr8:102953800-102959400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr8:102954600-102962800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:102955200-102956600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:102955200-102958000	Enhancers	Fetal Heart	heart
10	chr8:102955400-102956800	Weak transcription	Esophagus	oesophagus

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