Variant report

Variant	rs9402031
Chromosome Location	chr6:128564417-128564418
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:128560883..128563115-chr6:128564262..128566598,2	K562	blood:

Variant related genes	Relation type
ENSG00000152894	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10485160	0.82[CHB][hapmap];0.80[JPT][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11961542	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12055654	0.84[ASN][1000 genomes]
rs12055776	0.81[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1543376	0.82[CHB][hapmap];0.80[JPT][hapmap];0.81[ASN][1000 genomes]
rs17055472	0.81[CHB][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs17055477	0.81[CHB][hapmap];0.80[JPT][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2073161	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2076572	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3813371	0.80[JPT][hapmap]
rs3813373	0.80[JPT][hapmap]
rs4140541	0.81[CHB][hapmap];0.80[JPT][hapmap];0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4140542	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4483000	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61422755	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61583694	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6928143	0.81[CHB][hapmap]
rs6930547	0.90[ASN][1000 genomes]
rs6933029	0.80[JPT][hapmap]
rs6938118	0.80[JPT][hapmap]
rs730202	0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73590673	0.84[ASN][1000 genomes]
rs742736	0.81[CHB][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7753945	0.80[JPT][hapmap]
rs7755473	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7755836	0.81[CHB][hapmap];0.80[JPT][hapmap];0.80[ASN][1000 genomes]
rs7773849	0.82[CHB][hapmap];0.80[JPT][hapmap];0.80[ASN][1000 genomes]
rs9321113	0.82[CHB][hapmap];0.80[JPT][hapmap];0.81[YRI][hapmap];0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9372886	0.82[CHB][hapmap];0.80[JPT][hapmap];0.81[YRI][hapmap];0.84[ASN][1000 genomes]
rs9372887	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9375553	0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs9375554	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9375555	0.81[CHB][hapmap];0.81[YRI][hapmap];0.84[ASN][1000 genomes]
rs9375556	0.82[CHB][hapmap];0.80[JPT][hapmap];0.81[YRI][hapmap];0.84[ASN][1000 genomes]
rs9375557	0.84[ASN][1000 genomes]
rs9375558	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9385452	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9385454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9385455	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9388621	0.80[JPT][hapmap]
rs9388622	0.80[JPT][hapmap]
rs9388623	0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs9388624	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9388625	0.84[ASN][1000 genomes]
rs9388626	0.82[CHB][hapmap];0.80[JPT][hapmap];0.80[ASN][1000 genomes]
rs9388627	0.81[CHB][hapmap];0.80[JPT][hapmap];0.81[YRI][hapmap];0.84[ASN][1000 genomes]
rs9398864	0.90[ASN][1000 genomes]
rs9398865	0.92[JPT][hapmap];0.88[ASN][1000 genomes]
rs9398866	0.80[JPT][hapmap]
rs9398867	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9398868	0.81[CHB][hapmap];0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9402023	0.80[JPT][hapmap]
rs9402024	0.82[CHB][hapmap];0.80[JPT][hapmap];0.81[YRI][hapmap];0.80[ASN][1000 genomes]
rs9402025	0.87[CHB][hapmap];0.92[JPT][hapmap];0.99[ASN][1000 genomes]
rs9402027	0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9402028	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9402029	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9402030	0.81[CHB][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9402032	0.80[ASN][1000 genomes]
rs9784773	0.82[CHB][hapmap];0.80[JPT][hapmap];0.81[YRI][hapmap];0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9784880	0.81[CHB][hapmap];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033443	chr6:128306654-128899203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers 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 target site	8 gene(s)	inside rSNPs	diseases
2	nsv538440	chr6:128306654-128899203	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv886649	chr6:128399657-128808054	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv886651	chr6:128450019-128565778	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128488200-128565200	Weak transcription	Fetal Stomach	stomach
2	chr6:128492600-128567800	Weak transcription	Ovary	ovary
3	chr6:128520400-128573800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:128531200-128567800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:128531200-128573800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:128537600-128573800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:128540200-128564800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr6:128540400-128569400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr6:128551400-128565800	Weak transcription	Psoas Muscle	Psoas
10	chr6:128551400-128584400	Weak transcription	Pancreas	Pancrea
11	chr6:128553200-128573800	Weak transcription	NHLF	lung
12	chr6:128553800-128570600	Weak transcription	Liver	Liver
13	chr6:128555200-128584400	Weak transcription	HMEC	breast
14	chr6:128555600-128595800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr6:128555800-128564800	Weak transcription	Fetal Brain Female	brain
16	chr6:128559600-128570600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr6:128559800-128565600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr6:128561400-128564800	Weak transcription	Osteobl	bone
19	chr6:128561400-128567800	Weak transcription	Right Ventricle	heart
20	chr6:128561400-128573000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr6:128561400-128587000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr6:128561600-128567600	Weak transcription	Brain Angular Gyrus	brain
23	chr6:128561600-128569200	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr6:128561600-128573800	Weak transcription	Thymus	Thymus
25	chr6:128562400-128576600	Weak transcription	Duodenum Mucosa	Duodenum
26	chr6:128562600-128567400	Weak transcription	Brain Anterior Caudate	brain
27	chr6:128562600-128573600	Weak transcription	Primary T cells from cord blood	blood
28	chr6:128562800-128567600	Weak transcription	Brain Substantia Nigra	brain
29	chr6:128562800-128567600	Weak transcription	Fetal Intestine Large	intestine
30	chr6:128562800-128567800	Weak transcription	Right Atrium	heart
31	chr6:128562800-128568000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:128562800-128573000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr6:128562800-128573000	Weak transcription	Aorta	Aorta
34	chr6:128562800-128573800	Weak transcription	Gastric	stomach
35	chr6:128562800-128579800	Weak transcription	Left Ventricle	heart
36	chr6:128562800-128588200	Weak transcription	HUVEC	blood vessel
37	chr6:128563000-128570600	Weak transcription	HSMMtube	muscle
38	chr6:128563000-128573000	Weak transcription	NH-A	brain
39	chr6:128563000-128574000	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr6:128563000-128585400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr6:128563200-128567600	Weak transcription	Fetal Intestine Small	intestine
42	chr6:128563600-128564600	Strong transcription	Fetal Thymus	thymus
43	chr6:128563800-128566200	Weak transcription	HSMM	muscle
44	chr6:128563800-128567800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr6:128564000-128565400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:128564000-128566800	Enhancers	Fetal Heart	heart
47	chr6:128564200-128565000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr6:128564400-128564800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr6:128564400-128565000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr6:128564400-128565800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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