Variant report

Variant	rs9287901
Chromosome Location	chr2:169620615-169620616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10197317	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1063729	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12692886	0.86[MEX][hapmap]
rs12692887	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3732030	0.86[CHB][hapmap]
rs3843327	0.95[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3914919	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57805112	0.93[ASN][1000 genomes]
rs61386309	0.87[ASN][1000 genomes]
rs6433090	0.86[ASN][1000 genomes]
rs6433091	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7584527	0.86[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];0.86[JPT][hapmap];0.85[TSI][hapmap];0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915920	chr2:168851960-169696591	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9287901	C2orf77	cis	cerebellum	SCAN

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169565200-169622800	Weak transcription	Liver	Liver
2	chr2:169579600-169630200	Weak transcription	Aorta	Aorta
3	chr2:169579600-169630600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:169586000-169627600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:169587800-169623200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:169595200-169621000	Weak transcription	Brain Germinal Matrix	brain
7	chr2:169595200-169622800	Weak transcription	NHEK	skin
8	chr2:169597200-169635800	Weak transcription	Ovary	ovary
9	chr2:169598600-169622800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:169601600-169625800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr2:169604800-169627600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr2:169606000-169623000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:169606000-169630600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr2:169606000-169630600	Weak transcription	Adipose Nuclei	Adipose
15	chr2:169606200-169630400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:169606600-169630600	Weak transcription	Gastric	stomach
17	chr2:169606600-169632800	Weak transcription	Pancreas	Pancrea
18	chr2:169608000-169622000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:169608000-169625800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:169608200-169633800	Weak transcription	Psoas Muscle	Psoas
21	chr2:169608400-169626800	Weak transcription	Fetal Lung	lung
22	chr2:169608400-169627600	Weak transcription	HSMM	muscle
23	chr2:169608400-169632200	Weak transcription	HSMMtube	muscle
24	chr2:169608400-169633600	Weak transcription	Dnd41	blood
25	chr2:169609000-169628000	Weak transcription	Primary B cells from peripheral blood	blood
26	chr2:169609200-169636400	Weak transcription	Lung	lung
27	chr2:169609400-169633000	Weak transcription	Rectal Smooth Muscle	rectum
28	chr2:169609600-169634200	Weak transcription	Fetal Brain Male	brain
29	chr2:169610000-169625800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr2:169610000-169630600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr2:169610600-169622800	Weak transcription	Esophagus	oesophagus
32	chr2:169610800-169637400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr2:169611200-169636600	Weak transcription	HepG2	liver
34	chr2:169611600-169622800	Weak transcription	HMEC	breast
35	chr2:169611600-169625800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:169611600-169626800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:169612400-169623400	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr2:169612600-169622000	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr2:169612600-169622600	Weak transcription	Fetal Muscle Trunk	muscle
40	chr2:169612600-169625800	Weak transcription	Stomach Smooth Muscle	stomach
41	chr2:169612800-169622800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr2:169613400-169622800	Weak transcription	Thymus	Thymus
43	chr2:169613800-169621000	Weak transcription	Fetal Brain Female	brain
44	chr2:169614000-169620800	Weak transcription	GM12878-XiMat	blood
45	chr2:169614000-169622800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr2:169614000-169625800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:169614200-169622000	Weak transcription	Small Intestine	intestine
48	chr2:169614200-169623200	Weak transcription	Right Ventricle	heart
49	chr2:169614200-169628000	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr2:169614400-169621000	Weak transcription	Fetal Intestine Large	intestine

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