Variant report

Variant	rs13361485
Chromosome Location	chr5:95179960-95179961
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:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:95177864..95180977-chr5:95197821..95200225,3	MCF-7	breast:
2	chr5:95116606..95117631-chr5:95177527..95180416,16	MCF-7	breast:
3	chr5:95137350..95139988-chr5:95179916..95183018,3	MCF-7	breast:
4	chr5:95053439..95055836-chr5:95177234..95179999,3	MCF-7	breast:
5	chr5:95122048..95125672-chr5:95179642..95182375,3	MCF-7	breast:
6	chr5:95061804..95065801-chr5:95176790..95180360,3	MCF-7	breast:
7	chr5:95064707..95068604-chr5:95176347..95180425,6	MCF-7	breast:
8	chr5:95144281..95145870-chr5:95178022..95180919,2	MCF-7	breast:
9	chr5:95065827..95067681-chr5:95178770..95180353,2	K562	blood:
10	chr5:94978692..94981484-chr5:95178419..95181281,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf27-1	chr5:95179854-95180339	XLOC_004478
2	lnc-C5orf27-1	chr5:95179752-95180339	XLOC_004478
3	lnc-C5orf27-1	chr5:95179854-95180271	XLOC_004478

No data

Variant related genes	Relation type
ENSG00000164292	Chromatin interaction
ENSG00000250240	Chromatin interaction

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

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

rs_ID	r²[population]
rs10069749	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10077757	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13361488	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2161313	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2547996	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35234911	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3756704	0.95[ASN][1000 genomes]
rs3797206	0.84[ASN][1000 genomes]
rs60868839	0.81[ASN][1000 genomes]
rs6556890	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6873668	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6875489	0.87[ASN][1000 genomes]
rs7709560	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7725607	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs918469	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs918470	0.99[ASN][1000 genomes]
rs9314160	0.86[ASN][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	nsv830409	chr5:95006686-95204496	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1015180	chr5:95134357-95286446	Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95171800-95185800	Weak transcription	Pancreas	Pancrea
2	chr5:95172200-95180400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr5:95173400-95180800	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr5:95174400-95180000	Enhancers	Primary B cells from cord blood	blood
5	chr5:95175800-95182200	Weak transcription	Esophagus	oesophagus
6	chr5:95176000-95180200	Weak transcription	Gastric	stomach
7	chr5:95176200-95181200	Enhancers	Placenta	Placenta
8	chr5:95176400-95180400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:95176800-95180000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr5:95177000-95180200	Enhancers	Adipose Nuclei	Adipose
11	chr5:95177000-95180600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr5:95177000-95181400	Enhancers	Primary hematopoietic stem cells	blood
13	chr5:95177200-95180000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr5:95177200-95180200	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr5:95177600-95180000	Enhancers	K562	blood
16	chr5:95177800-95192200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr5:95178000-95180000	Enhancers	Fetal Intestine Large	intestine
18	chr5:95178200-95180000	Enhancers	Primary T cells from cord blood	blood
19	chr5:95178200-95182200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr5:95178400-95180000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr5:95178400-95180000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr5:95178400-95188400	Weak transcription	Stomach Mucosa	stomach
23	chr5:95178600-95180000	Enhancers	Fetal Intestine Small	intestine
24	chr5:95178600-95180000	Enhancers	Right Atrium	heart
25	chr5:95178800-95180000	Enhancers	A549	lung
26	chr5:95179000-95186200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr5:95179000-95206000	Weak transcription	Spleen	Spleen
28	chr5:95179200-95180000	Enhancers	Brain Hippocampus Middle	brain
29	chr5:95179200-95180200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr5:95179200-95180200	Enhancers	Hela-S3	cervix
31	chr5:95179200-95182200	Weak transcription	Thymus	Thymus
32	chr5:95179200-95182200	Weak transcription	HUVEC	blood vessel
33	chr5:95179200-95184200	Weak transcription	HSMM	muscle
34	chr5:95179200-95185800	Weak transcription	Lung	lung
35	chr5:95179400-95180400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr5:95179400-95180400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:95179400-95180600	Enhancers	Dnd41	blood
38	chr5:95179400-95181400	Weak transcription	HepG2	liver
39	chr5:95179400-95181600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr5:95179400-95181600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr5:95179400-95182000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr5:95179400-95182200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr5:95179400-95182200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr5:95179400-95182200	Weak transcription	NHLF	lung
45	chr5:95179400-95182400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:95179400-95182400	Weak transcription	Brain Anterior Caudate	brain
47	chr5:95179400-95182400	Weak transcription	Brain Substantia Nigra	brain
48	chr5:95179400-95183000	Weak transcription	Fetal Heart	heart
49	chr5:95179400-95183600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr5:95179400-95184600	Weak transcription	NH-A	brain

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