Variant report

Variant	rs920800
Chromosome Location	chr7:4112268-4112269
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10226621	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10238275	0.81[EUR][1000 genomes]
rs10240845	0.86[EUR][1000 genomes]
rs10248212	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10248826	0.81[EUR][1000 genomes]
rs10270792	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10277661	0.81[EUR][1000 genomes]
rs10277830	0.86[EUR][1000 genomes]
rs10485859	0.81[EUR][1000 genomes]
rs12386628	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs1443646	0.81[EUR][1000 genomes]
rs2091406	0.86[EUR][1000 genomes]
rs2103233	0.86[EUR][1000 genomes]
rs2342500	0.81[EUR][1000 genomes]
rs28488873	0.86[EUR][1000 genomes]
rs28494068	1.00[EUR][1000 genomes]
rs58873518	0.84[EUR][1000 genomes]
rs59136980	0.81[EUR][1000 genomes]
rs59373847	0.81[EUR][1000 genomes]
rs59763818	0.81[EUR][1000 genomes]
rs61030165	0.81[EUR][1000 genomes]
rs61489118	0.81[EUR][1000 genomes]
rs61735696	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6965091	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs73299001	0.81[EUR][1000 genomes]
rs73300926	0.81[EUR][1000 genomes]
rs73300951	0.81[EUR][1000 genomes]
rs73300972	0.81[EUR][1000 genomes]
rs73300977	0.81[EUR][1000 genomes]
rs73300989	0.81[EUR][1000 genomes]
rs7456402	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7780738	1.00[EUR][1000 genomes]
rs7786018	0.81[EUR][1000 genomes]
rs7792644	0.81[EUR][1000 genomes]
rs7793027	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs7805307	0.81[EUR][1000 genomes]
rs7806117	0.81[EUR][1000 genomes]
rs7808027	0.81[EUR][1000 genomes]
rs920801	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs930534	0.81[EUR][1000 genomes]
rs930535	0.81[EUR][1000 genomes]
rs930536	0.81[EUR][1000 genomes]
rs930537	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021650	chr7:3665232-4577439	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1029406	chr7:3860894-4477095	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv538685	chr7:3860894-4477095	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1026410	chr7:3869104-4383606	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1025497	chr7:3905444-4176032	Enhancers Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv538686	chr7:3905444-4176032	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv464274	chr7:3955516-4613607	Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv464275	chr7:3955516-4613607	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv464276	chr7:3955516-4613607	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv464277	chr7:3955516-4613607	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv464278	chr7:3955516-4613607	Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv605939	chr7:3955516-4613607	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv1019305	chr7:3991646-4276004	Enhancers Weak transcription Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv1033687	chr7:4006020-4267871	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv538688	chr7:4006020-4267871	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv917252	chr7:4017819-4374090	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv527624	chr7:4027536-4424054	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv1022794	chr7:4063874-4137968	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv538689	chr7:4063874-4137968	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv869540	chr7:4063875-4302040	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
21	nsv1028689	chr7:4078345-4166552	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
22	nsv538690	chr7:4078345-4166552	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
23	nsv1018462	chr7:4097676-4173613	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
24	nsv1016507	chr7:4105420-4255439	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
25	nsv538691	chr7:4105420-4255439	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 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	chr7:4088800-4129400	Weak transcription	Right Ventricle	heart
2	chr7:4096000-4116400	Weak transcription	Adipose Nuclei	Adipose
3	chr7:4103000-4125600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:4104800-4116400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr7:4105200-4117000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:4105200-4120200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr7:4106600-4117000	Weak transcription	Fetal Brain Female	brain
8	chr7:4106800-4113400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr7:4107800-4120200	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr7:4109200-4116200	Weak transcription	Fetal Intestine Small	intestine
11	chr7:4109200-4118200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr7:4109600-4112400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:4109600-4112800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr7:4109600-4122000	Weak transcription	Esophagus	oesophagus
15	chr7:4109800-4116200	Weak transcription	Spleen	Spleen
16	chr7:4110200-4116200	Weak transcription	Pancreas	Pancrea
17	chr7:4110200-4116400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:4110200-4118400	Weak transcription	Gastric	stomach
19	chr7:4110200-4129400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:4110600-4116200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:4111200-4112600	Enhancers	Fetal Muscle Leg	muscle
22	chr7:4111200-4113000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:4111400-4119600	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr7:4111600-4113400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:4111600-4116200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr7:4111800-4112400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr7:4111800-4112400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:4111800-4112400	Strong transcription	Aorta	Aorta
29	chr7:4111800-4112600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr7:4111800-4113400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr7:4112000-4116600	Weak transcription	Fetal Stomach	stomach
32	chr7:4112200-4113000	Enhancers	Fetal Muscle Trunk	muscle
33	chr7:4112200-4116400	Weak transcription	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links