Variant report

Variant	rs4776625
Chromosome Location	chr15:73360107-73360108
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	chr15:73352462..73355061-chr15:73359053..73360956,2	MCF-7	breast:
2	chr15:73356525..73360663-chr15:73369090..73372368,3	MCF-7	breast:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1023924	0.81[AMR][1000 genomes]
rs1038137	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10467948	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11072403	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13379875	0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1964543	0.80[EUR][1000 genomes]
rs2169951	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4132536	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4545783	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4609810	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4776624	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4777590	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs55836604	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55925663	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs56269104	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56377702	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62016797	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62016803	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs62016805	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs62016806	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62016808	0.80[EUR][1000 genomes]
rs62016809	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs62016811	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62016813	0.80[EUR][1000 genomes]
rs62016814	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62016849	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7165610	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8026121	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9972347	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][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	esv3352103	chr15:73191535-73454001	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv482421	chr15:73279141-73426897	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
3	nsv904338	chr15:73313691-73483718	Enhancers Active TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv517966	chr15:73349633-73488753	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv525462	chr15:73349633-73563495	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73349400-73367000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr15:73352000-73365000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr15:73353800-73363400	Weak transcription	Aorta	Aorta
4	chr15:73353800-73366000	Weak transcription	Fetal Intestine Large	intestine
5	chr15:73353800-73367400	Weak transcription	Fetal Intestine Small	intestine
6	chr15:73354400-73364800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr15:73355200-73365200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr15:73355600-73365800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr15:73356600-73360200	Weak transcription	Brain Anterior Caudate	brain
10	chr15:73358000-73367000	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr15:73359200-73366000	Weak transcription	Fetal Brain Male	brain
12	chr15:73359200-73370600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr15:73359400-73360200	Weak transcription	Brain Angular Gyrus	brain
14	chr15:73359400-73361000	Weak transcription	Brain Substantia Nigra	brain
15	chr15:73359600-73365400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:73359600-73367400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr15:73359800-73365600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr15:73360000-73360400	Weak transcription	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links