Variant report

Variant	rs73692208
Chromosome Location	chr8:89257036-89257037
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:106915661..106917953-chr8:89256955..89259785,2	MCF-7	breast:
2	chr8:89251063..89254156-chr8:89255310..89258377,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000228966	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs17666351	0.81[AMR][1000 genomes]
rs17666560	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17666825	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17722705	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17723163	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17728649	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28904602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28904630	0.81[AMR][1000 genomes]
rs55799901	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57187913	0.80[EUR][1000 genomes]
rs57837867	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59592564	0.89[AMR][1000 genomes]
rs6993842	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73692207	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73694276	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7835443	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][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	nsv1029898	chr8:88837956-89606641	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1030028	chr8:89060085-89733470	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1019111	chr8:89186908-89475460	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv831386	chr8:89209788-89403546	Enhancers Genic enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv891170	chr8:89227970-89298199	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89239000-89260800	Weak transcription	Aorta	Aorta
2	chr8:89250000-89259600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:89252600-89257600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr8:89252600-89264400	Weak transcription	Fetal Heart	heart
5	chr8:89254600-89257200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr8:89254600-89257400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr8:89254800-89257200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr8:89254800-89257200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr8:89254800-89257600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr8:89255400-89258000	Enhancers	Fetal Brain Female	brain
11	chr8:89255600-89257400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:89255600-89258000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr8:89255800-89258200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr8:89256000-89259600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr8:89256000-89261200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr8:89256200-89258600	Weak transcription	Colon Smooth Muscle	Colon
17	chr8:89256400-89258400	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr8:89256400-89259200	Weak transcription	Fetal Lung	lung
19	chr8:89256600-89259600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr8:89256800-89257600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr8:89256800-89257800	Weak transcription	Brain Germinal Matrix	brain
22	chr8:89256800-89259200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr8:89256800-89260000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr8:89256800-89264400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:89257000-89258200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:89257000-89261600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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