Variant report

Variant	rs9885082
Chromosome Location	chr5:108246854-108246855
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10038669	0.84[ASN][1000 genomes]
rs10040696	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10045220	0.82[ASN][1000 genomes]
rs10060694	0.82[ASN][1000 genomes]
rs10062204	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10063167	0.87[ASN][1000 genomes]
rs10073668	0.84[ASN][1000 genomes]
rs10477431	0.82[ASN][1000 genomes]
rs13180513	0.85[ASN][1000 genomes]
rs2081126	0.82[ASN][1000 genomes]
rs2081129	0.82[ASN][1000 genomes]
rs28637651	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs34125469	0.85[ASN][1000 genomes]
rs4604227	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56373044	0.82[ASN][1000 genomes]
rs6594338	0.80[ASN][1000 genomes]
rs6874229	0.85[ASN][1000 genomes]
rs6880284	0.87[ASN][1000 genomes]
rs6895027	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7712834	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7725391	0.82[ASN][1000 genomes]
rs7735235	0.82[ASN][1000 genomes]
rs9326748	0.85[ASN][1000 genomes]
rs9885168	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1016343	chr5:108220116-108364687	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv882691	chr5:108229760-108366473	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108183800-108260400	Weak transcription	Ovary	ovary
2	chr5:108194600-108260000	Weak transcription	Fetal Intestine Large	intestine
3	chr5:108197000-108268200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr5:108199200-108271400	Weak transcription	Aorta	Aorta
5	chr5:108203800-108323400	Weak transcription	Primary B cells from cord blood	blood
6	chr5:108208200-108268800	Weak transcription	Primary T cells from cord blood	blood
7	chr5:108214200-108272200	Weak transcription	Gastric	stomach
8	chr5:108217400-108253200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr5:108217600-108323200	Weak transcription	Left Ventricle	heart
10	chr5:108221400-108280600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:108223400-108247000	Weak transcription	Brain Substantia Nigra	brain
12	chr5:108228600-108247600	Weak transcription	Liver	Liver
13	chr5:108229600-108269800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:108230200-108302400	Weak transcription	HSMM	muscle
15	chr5:108230600-108249400	Weak transcription	Fetal Muscle Leg	muscle
16	chr5:108230600-108260000	Weak transcription	Fetal Intestine Small	intestine
17	chr5:108235000-108253200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:108235200-108252400	Weak transcription	NHEK	skin
19	chr5:108235200-108253000	Weak transcription	Adipose Nuclei	Adipose
20	chr5:108236800-108253400	Weak transcription	NH-A	brain
21	chr5:108238200-108247400	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr5:108240400-108252800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:108242200-108249400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:108242200-108271000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:108242800-108252800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:108244200-108295000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr5:108244600-108248400	Weak transcription	HMEC	breast
28	chr5:108246200-108247000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:108246400-108247200	Strong transcription	Fetal Lung	lung
30	chr5:108246400-108248800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr5:108246600-108247600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr5:108246600-108251000	Weak transcription	Psoas Muscle	Psoas
33	chr5:108246800-108253000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links