Variant report

Variant	rs3737146
Chromosome Location	chr9:101810159-101810160
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16918141	0.89[CHB][hapmap];0.82[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16918194	1.00[EUR][1000 genomes]
rs16918218	1.00[EUR][1000 genomes]
rs16918220	1.00[EUR][1000 genomes]
rs16918228	1.00[EUR][1000 genomes]
rs16918238	1.00[EUR][1000 genomes]
rs16918245	1.00[EUR][1000 genomes]
rs2274960	1.00[EUR][1000 genomes]
rs3780619	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3824512	0.82[JPT][hapmap];1.00[EUR][1000 genomes]
rs7022519	0.89[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs7863250	0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs914993	0.80[CHD][hapmap]

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	nsv466442	chr9:101788522-101816399	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv614954	chr9:101788522-101816399	Strong transcription Genic enhancers Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv893618	chr9:101800106-101886071	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101761600-101814400	Weak transcription	Gastric	stomach
2	chr9:101782000-101819800	Weak transcription	Colonic Mucosa	Colon
3	chr9:101789000-101812000	Weak transcription	Esophagus	oesophagus
4	chr9:101793800-101837600	Weak transcription	Psoas Muscle	Psoas
5	chr9:101798200-101811400	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr9:101798400-101819800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr9:101799200-101814600	Weak transcription	Pancreas	Pancrea
8	chr9:101804000-101820000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr9:101805800-101819400	Strong transcription	Adipose Nuclei	Adipose
10	chr9:101805800-101820600	Weak transcription	Right Ventricle	heart
11	chr9:101806400-101810600	Strong transcription	Ovary	ovary
12	chr9:101806600-101817000	Weak transcription	Left Ventricle	heart
13	chr9:101807000-101831800	Strong transcription	Fetal Muscle Trunk	muscle
14	chr9:101807200-101811400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr9:101807400-101811000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr9:101807400-101811600	Weak transcription	NHDF-Ad	bronchial
17	chr9:101807400-101814200	Weak transcription	Small Intestine	intestine
18	chr9:101807400-101819000	Strong transcription	Fetal Stomach	stomach
19	chr9:101807600-101810400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:101807600-101811800	Weak transcription	Lung	lung
21	chr9:101807600-101812000	Weak transcription	Aorta	Aorta
22	chr9:101807600-101831800	Strong transcription	Fetal Muscle Leg	muscle
23	chr9:101807800-101819800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr9:101808400-101810800	Strong transcription	Skeletal Muscle Male	skeletal muscle
25	chr9:101808400-101817200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr9:101808600-101812600	Weak transcription	HSMMtube	muscle
27	chr9:101808800-101811200	Enhancers	Placenta	Placenta
28	chr9:101809000-101811000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr9:101809200-101811200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr9:101809200-101812200	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr9:101809200-101821600	Weak transcription	Brain Anterior Caudate	brain
32	chr9:101809600-101810400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr9:101809600-101811200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr9:101809600-101811400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr9:101809800-101810600	Genic enhancers	Stomach Smooth Muscle	stomach
36	chr9:101809800-101811200	Weak transcription	Rectal Smooth Muscle	rectum
37	chr9:101809800-101815000	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr9:101810000-101810600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr9:101810000-101811400	Weak transcription	K562	blood
40	chr9:101810000-101813000	Strong transcription	Colon Smooth Muscle	Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links