Variant report

Variant	rs7756711
Chromosome Location	chr6:161443456-161443457
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1001808	0.83[AFR][1000 genomes]
rs12203648	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13200744	0.84[CHB][hapmap]
rs1562027	0.95[CEU][hapmap];0.85[CHB][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1822520	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs35894036	0.84[ASN][1000 genomes]
rs3734461	0.89[CHB][hapmap]
rs3757021	0.85[CEU][hapmap]
rs4324757	1.00[CEU][hapmap];0.93[YRI][hapmap];0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4709485	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.89[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs4709488	0.82[CEU][hapmap];0.87[YRI][hapmap];0.82[AFR][1000 genomes]
rs588284	0.84[ASN][1000 genomes]
rs589238	0.94[CHB][hapmap];0.88[ASN][1000 genomes]
rs590988	0.90[CHB][hapmap]
rs593184	0.84[ASN][1000 genomes]
rs594555	0.94[CHB][hapmap];0.82[JPT][hapmap];0.96[ASN][1000 genomes]
rs594602	1.00[CHB][hapmap];0.89[JPT][hapmap];0.96[ASN][1000 genomes]
rs602837	0.82[YRI][hapmap]
rs610638	0.80[AFR][1000 genomes]
rs619831	0.85[ASN][1000 genomes]
rs628075	0.90[CHB][hapmap];0.84[ASN][1000 genomes]
rs629015	0.82[ASN][1000 genomes]
rs630006	1.00[CHB][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs630430	0.87[ASN][1000 genomes]
rs643706	0.95[CHB][hapmap];0.87[ASN][1000 genomes]
rs644110	0.90[CHB][hapmap];0.83[ASN][1000 genomes]
rs645406	0.90[CHB][hapmap];0.83[ASN][1000 genomes]
rs657616	0.90[CHB][hapmap]
rs671335	0.93[ASN][1000 genomes]
rs673468	0.85[YRI][hapmap]
rs674220	0.84[ASN][1000 genomes]
rs675538	0.84[ASN][1000 genomes]
rs685939	0.84[ASN][1000 genomes]
rs686392	0.84[ASN][1000 genomes]
rs686755	0.84[ASN][1000 genomes]
rs6901173	1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[ASN][1000 genomes]
rs6901968	1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[ASN][1000 genomes]
rs6913867	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs787784	0.85[ASN][1000 genomes]
rs796835	0.84[ASN][1000 genomes]
rs9295134	0.84[CHB][hapmap]
rs9347478	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9355327	1.00[CHB][hapmap];0.84[JPT][hapmap];0.95[ASN][1000 genomes]
rs9365245	0.82[AMR][1000 genomes]
rs9458102	0.84[CHB][hapmap]

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	nsv1030045	chr6:161359075-161562255	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv886817	chr6:161371621-161846654	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	esv3381361	chr6:161373617-161864101	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1023982	chr6:161382188-161549831	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161414200-161458200	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr6:161414400-161469600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr6:161414600-161457400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:161415600-161450000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr6:161416600-161475200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr6:161417400-161449000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:161418000-161448800	Weak transcription	Lung	lung
8	chr6:161428600-161455800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr6:161432200-161450000	Weak transcription	HMEC	breast
10	chr6:161432200-161450400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:161432200-161451200	Weak transcription	NHEK	skin
12	chr6:161432600-161455400	Weak transcription	Fetal Intestine Large	intestine
13	chr6:161433000-161449000	Weak transcription	HSMM	muscle
14	chr6:161433000-161458000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr6:161433200-161448800	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr6:161433200-161450000	Weak transcription	Aorta	Aorta
17	chr6:161433200-161459200	Weak transcription	Fetal Stomach	stomach
18	chr6:161433400-161446200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr6:161433400-161450000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:161433400-161455600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:161433400-161455800	Weak transcription	Fetal Muscle Leg	muscle
22	chr6:161433400-161455800	Weak transcription	Stomach Smooth Muscle	stomach
23	chr6:161433400-161459000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr6:161433600-161458200	Weak transcription	Fetal Brain Female	brain
25	chr6:161433600-161459600	Weak transcription	Brain Germinal Matrix	brain
26	chr6:161433800-161444400	Weak transcription	NHDF-Ad	bronchial
27	chr6:161433800-161448400	Weak transcription	NH-A	brain
28	chr6:161433800-161451000	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr6:161434000-161449800	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr6:161434000-161455600	Weak transcription	Adipose Nuclei	Adipose
31	chr6:161434000-161459000	Weak transcription	Brain Hippocampus Middle	brain
32	chr6:161434200-161443800	Weak transcription	Osteobl	bone
33	chr6:161434200-161450000	Weak transcription	Primary B cells from peripheral blood	blood
34	chr6:161434800-161458200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr6:161435000-161448800	Weak transcription	Gastric	stomach
36	chr6:161435000-161448800	Weak transcription	Pancreas	Pancrea
37	chr6:161435000-161449600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:161435000-161452200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr6:161435000-161458000	Weak transcription	Fetal Muscle Trunk	muscle
40	chr6:161435000-161458800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr6:161435000-161490400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr6:161435200-161446800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr6:161435200-161446800	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr6:161435200-161450400	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr6:161435200-161454800	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr6:161435200-161455800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr6:161435400-161450400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr6:161436800-161443600	Weak transcription	Spleen	Spleen
49	chr6:161436800-161455600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr6:161437000-161444400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links