Variant report

Variant	rs190960
Chromosome Location	chr17:63112939-63112940
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	chr17:63104937..63106962-chr17:63110869..63114736,3	MCF-7	breast:

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs28376193	1.00[EUR][1000 genomes]
rs28669831	1.00[EUR][1000 genomes]
rs28696681	1.00[EUR][1000 genomes]
rs28852789	1.00[EUR][1000 genomes]
rs299833	1.00[EUR][1000 genomes]
rs299836	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4129025	1.00[EUR][1000 genomes]
rs59911976	1.00[EUR][1000 genomes]
rs8067101	1.00[EUR][1000 genomes]
rs8072705	1.00[EUR][1000 genomes]
rs9889760	1.00[EUR][1000 genomes]
rs9891825	1.00[EUR][1000 genomes]
rs9892174	1.00[EUR][1000 genomes]
rs9903465	1.00[EUR][1000 genomes]
rs9907340	1.00[EUR][1000 genomes]
rs9915448	1.00[EUR][1000 genomes]
rs9915947	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066765	chr17:62649313-63124303	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv530764	chr17:62939944-63278472	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:63103000-63118800	Weak transcription	Aorta	Aorta
2	chr17:63103200-63118400	Weak transcription	Left Ventricle	heart
3	chr17:63103200-63118800	Weak transcription	Right Atrium	heart
4	chr17:63103400-63118600	Weak transcription	Brain Anterior Caudate	brain
5	chr17:63103400-63118600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr17:63103800-63118600	Weak transcription	Psoas Muscle	Psoas
7	chr17:63104000-63118600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr17:63104000-63118800	Weak transcription	Colon Smooth Muscle	Colon
9	chr17:63104200-63118600	Weak transcription	Brain Hippocampus Middle	brain
10	chr17:63104400-63118600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr17:63106200-63119000	Weak transcription	Fetal Lung	lung
12	chr17:63106400-63118600	Weak transcription	Adipose Nuclei	Adipose
13	chr17:63108000-63118600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr17:63111400-63113800	Enhancers	Primary hematopoietic stem cells	blood
15	chr17:63111400-63114000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr17:63111400-63114000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr17:63112400-63113200	Weak transcription	Primary B cells from peripheral blood	blood
18	chr17:63112400-63113600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr17:63112400-63113800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr17:63112400-63118200	Weak transcription	K562	blood
21	chr17:63112400-63118600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr17:63112400-63119000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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