Variant report

Variant	rs4779677
Chromosome Location	chr15:30212379-30212380
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	chr15:30112803..30116771-chr15:30211280..30215308,10	MCF-7	breast:
2	chr15:30113867..30115959-chr15:30211073..30213132,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000104067	Chromatin interaction
ENSG00000259523	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs1001877	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12592270	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12594438	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12594461	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1357386	0.97[ASN][1000 genomes]
rs1357387	0.97[ASN][1000 genomes]
rs1357388	0.97[ASN][1000 genomes]
rs1357389	0.84[ASN][1000 genomes]
rs1403355	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1464564	0.84[ASN][1000 genomes]
rs1464565	0.84[ASN][1000 genomes]
rs1522640	0.84[ASN][1000 genomes]
rs1522643	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1522791	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1522792	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1522794	0.97[ASN][1000 genomes]
rs1533860	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1631472	0.97[ASN][1000 genomes]
rs1632356	0.97[ASN][1000 genomes]
rs1718977	0.84[ASN][1000 genomes]
rs1718985	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1718986	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1718987	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1718988	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1718989	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1718990	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1718991	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1718993	0.96[ASN][1000 genomes]
rs1718997	0.92[ASN][1000 genomes]
rs1718998	0.95[ASN][1000 genomes]
rs1718999	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1719001	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1719040	0.84[ASN][1000 genomes]
rs1719041	0.84[ASN][1000 genomes]
rs1719337	0.99[ASN][1000 genomes]
rs1719338	0.99[ASN][1000 genomes]
rs1719341	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1719343	0.98[ASN][1000 genomes]
rs1719345	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1719348	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1719349	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1719350	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1719351	0.97[ASN][1000 genomes]
rs1719352	0.97[ASN][1000 genomes]
rs1719353	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1719354	0.96[ASN][1000 genomes]
rs1719358	0.97[ASN][1000 genomes]
rs1719359	0.97[ASN][1000 genomes]
rs1719360	0.97[ASN][1000 genomes]
rs1719361	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1719363	0.96[EUR][1000 genomes]
rs2103056	0.97[ASN][1000 genomes]
rs2253906	0.97[ASN][1000 genomes]
rs2461657	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2948555	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34866689	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4503741	0.82[ASN][1000 genomes]
rs4779461	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4779672	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4779673	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4779674	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4779675	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4779676	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4779681	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72625154	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs939976	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs939977	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs939978	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs939979	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv995038	chr15:29744279-30366124	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1038495	chr15:29825859-30351687	Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv542293	chr15:29825859-30351687	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	esv2422463	chr15:30003189-30215336	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv903754	chr15:30023454-30382120	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
6	nsv903755	chr15:30036085-30351434	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	nsv482572	chr15:30118905-30304529	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv456739	chr15:30178614-30366247	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv568716	chr15:30178614-30366247	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv431371	chr15:30193316-31012794	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30206400-30212400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr15:30206800-30216400	Weak transcription	HSMM	muscle
3	chr15:30207000-30212600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:30207000-30212600	Weak transcription	Placenta	Placenta
5	chr15:30207200-30212400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr15:30207200-30212600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr15:30207200-30212800	Weak transcription	Pancreas	Pancrea
8	chr15:30207200-30213000	Weak transcription	Right Ventricle	heart
9	chr15:30207200-30213800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr15:30207200-30216400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr15:30207200-30216800	Weak transcription	Fetal Kidney	kidney
12	chr15:30209200-30213800	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr15:30210000-30212600	Weak transcription	Fetal Heart	heart
14	chr15:30210000-30213600	Weak transcription	Esophagus	oesophagus
15	chr15:30210400-30212800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr15:30210600-30212600	Enhancers	A549	lung
17	chr15:30210800-30213200	Enhancers	Brain Anterior Caudate	brain
18	chr15:30211000-30213800	Enhancers	Brain Hippocampus Middle	brain
19	chr15:30211200-30212800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr15:30211200-30212800	Enhancers	Brain Substantia Nigra	brain
21	chr15:30211200-30213800	Enhancers	Brain Angular Gyrus	brain
22	chr15:30211200-30213800	Enhancers	Brain Cingulate Gyrus	brain
23	chr15:30211400-30212400	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr15:30211400-30212600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr15:30211400-30212800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:30211400-30213000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr15:30211400-30213000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr15:30211400-30213000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:30211400-30214400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr15:30211600-30212600	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr15:30211600-30212600	Enhancers	NHEK	skin
32	chr15:30211600-30216000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr15:30211800-30213400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr15:30212000-30212800	Weak transcription	Lung	lung
35	chr15:30212000-30213000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr15:30212000-30213800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr15:30212000-30214400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr15:30212000-30214600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr15:30212200-30212800	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr15:30212200-30213000	Enhancers	HMEC	breast
41	chr15:30212200-30213800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr15:30212200-30213800	Enhancers	NH-A	brain
43	chr15:30212200-30214000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr15:30212200-30214000	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links