Variant report

Variant	rs2886527
Chromosome Location	chr3:61605739-61605740
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:56636052..56636690-chr3:61605499..61606152,3	MCF-7	breast:
2	chr17:56638650..56640955-chr3:61605126..61606787,2	MCF-7	breast:
3	chr17:56734668..56738970-chr3:61603973..61616839,24	MCF-7	breast:
4	chr17:56635071..56649233-chr3:61603708..61615718,44	MCF-7	breast:
5	chr19:33570754..33572499-chr3:61605256..61607373,2	MCF-7	breast:
6	chr17:56707443..56710525-chr3:61604154..61615875,21	MCF-7	breast:
7	chr17:56636075..56637147-chr3:61604733..61605975,7	MCF-7	breast:
8	chr17:56734480..56737024-chr3:61604208..61605747,2	MCF-7	breast:
9	chr17:56635069..56638406-chr3:61603721..61607564,12	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000266826	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000121101	Chromatin interaction
ENSG00000076650	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs13319699	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs13323186	1.00[AMR][1000 genomes]
rs13326667	0.82[YRI][hapmap];1.00[AMR][1000 genomes]
rs17065124	0.90[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17065131	1.00[ASW][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17065136	1.00[ASW][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28363967	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55849951	1.00[AMR][1000 genomes]
rs6798529	1.00[AMR][1000 genomes]
rs73838832	1.00[AMR][1000 genomes]
rs73838834	1.00[AMR][1000 genomes]
rs9810357	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9823399	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9827129	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9836164	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9839227	0.90[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9839369	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9868529	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9877032	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9879138	1.00[ASW][hapmap];1.00[MEX][hapmap]

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	nsv432423	chr3:61100255-61606060	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv834711	chr3:61413762-61612539	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1008615	chr3:61455419-61679037	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	esv2756995	chr3:61569557-61636156	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
5	esv2759153	chr3:61569557-61636156	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
6	esv35004	chr3:61570149-61626426	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
7	nsv822106	chr3:61577755-61631078	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
8	nsv1001611	chr3:61598148-61686809	Genic enhancers Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1000158	chr3:61598562-61682888	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	esv1800730	chr3:61599495-61620573	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS	Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:61581000-61609000	Weak transcription	NHEK	skin
2	chr3:61581400-61612200	Weak transcription	NHLF	lung
3	chr3:61581400-61613400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:61586400-61614200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:61587000-61611400	Weak transcription	HepG2	liver
6	chr3:61592800-61619800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr3:61594400-61610200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:61598200-61612200	Weak transcription	NHDF-Ad	bronchial
9	chr3:61598400-61611200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr3:61598800-61623200	Weak transcription	Aorta	Aorta
11	chr3:61601000-61611600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr3:61601200-61606800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr3:61602600-61606200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:61602800-61607000	Weak transcription	Fetal Stomach	stomach
15	chr3:61602800-61610200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr3:61602800-61613200	Weak transcription	NH-A	brain
17	chr3:61603000-61609800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr3:61603000-61610200	Weak transcription	Gastric	stomach
19	chr3:61603000-61612200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr3:61603000-61612200	Weak transcription	Lung	lung
21	chr3:61603000-61613600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr3:61603000-61613600	Weak transcription	Right Ventricle	heart
23	chr3:61603000-61614200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr3:61603000-61620000	Weak transcription	Left Ventricle	heart
25	chr3:61603200-61608600	Weak transcription	HSMM	muscle
26	chr3:61603200-61613000	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr3:61603200-61613200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr3:61603200-61623400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr3:61603400-61608600	Weak transcription	Fetal Muscle Leg	muscle
30	chr3:61603400-61609000	Weak transcription	Psoas Muscle	Psoas
31	chr3:61603400-61610600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr3:61603400-61612200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr3:61603400-61612200	Weak transcription	Right Atrium	heart
34	chr3:61603400-61613400	Weak transcription	Fetal Lung	lung
35	chr3:61603400-61613400	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr3:61603400-61613600	Weak transcription	Fetal Kidney	kidney
37	chr3:61603400-61615400	Weak transcription	HSMMtube	muscle
38	chr3:61603400-61620400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr3:61603400-61622600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr3:61603600-61612000	Weak transcription	Colon Smooth Muscle	Colon
41	chr3:61603600-61622800	Weak transcription	Ovary	ovary
42	chr3:61603800-61607600	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr3:61603800-61609400	Weak transcription	Fetal Intestine Large	intestine
44	chr3:61603800-61612200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:61604200-61607600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr3:61604200-61609600	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr3:61604200-61612200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr3:61604600-61611800	Weak transcription	Fetal Brain Male	brain
49	chr3:61605000-61605800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr3:61605000-61606200	Enhancers	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links