Variant report

Variant	rs56024732
Chromosome Location	chr6:2378156-2378157
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1016500	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10793836	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11242767	0.82[ASN][1000 genomes]
rs11759415	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12197998	0.83[ASN][1000 genomes]
rs12213061	0.82[ASN][1000 genomes]
rs13218890	0.83[ASN][1000 genomes]
rs1883586	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1883587	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1883588	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1883589	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1883590	0.82[ASN][1000 genomes]
rs2073002	0.81[ASN][1000 genomes]
rs2092403	0.83[ASN][1000 genomes]
rs4281006	0.84[ASN][1000 genomes]
rs4354194	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4413658	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4959183	0.84[ASN][1000 genomes]
rs4959649	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4959655	0.84[ASN][1000 genomes]
rs4959656	0.84[ASN][1000 genomes]
rs4959657	0.84[ASN][1000 genomes]
rs4959660	0.82[ASN][1000 genomes]
rs4959664	0.83[ASN][1000 genomes]
rs6907369	0.84[ASN][1000 genomes]
rs6920321	0.84[ASN][1000 genomes]
rs6925653	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6940450	0.84[ASN][1000 genomes]
rs7449538	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs764343	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs764344	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9503152	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9503158	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9503160	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9503162	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
2	nsv883388	chr6:2093432-2514911	Strong transcription Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
3	nsv883389	chr6:2093432-2776303	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
4	nsv1021573	chr6:2246721-2832408	Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
5	nsv538102	chr6:2246721-2832408	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
6	nsv883390	chr6:2265344-2584919	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv883391	chr6:2282747-2507448	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	esv3356254	chr6:2374553-2378751	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
9	nsv1016878	chr6:2375784-2680476	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2356200-2382200	Weak transcription	Aorta	Aorta
2	chr6:2356600-2382800	Weak transcription	Psoas Muscle	Psoas
3	chr6:2360400-2379600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:2362400-2391800	Weak transcription	Fetal Intestine Small	intestine
5	chr6:2362400-2397200	Weak transcription	Liver	Liver
6	chr6:2362800-2397200	Weak transcription	Left Ventricle	heart
7	chr6:2370200-2389000	Weak transcription	Esophagus	oesophagus
8	chr6:2376400-2378400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr6:2376600-2378800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:2376600-2380200	Enhancers	HSMM	muscle
11	chr6:2376800-2378200	Enhancers	NH-A	brain
12	chr6:2376800-2380400	Enhancers	HMEC	breast
13	chr6:2376800-2380400	Enhancers	NHDF-Ad	bronchial
14	chr6:2376800-2380600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:2376800-2389000	Weak transcription	Pancreas	Pancrea
16	chr6:2377000-2382600	Weak transcription	Gastric	stomach
17	chr6:2377400-2378200	Enhancers	Colon Smooth Muscle	Colon
18	chr6:2377400-2378200	Enhancers	Rectal Smooth Muscle	rectum
19	chr6:2377600-2378200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:2377600-2378200	Enhancers	A549	lung
21	chr6:2377600-2378600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr6:2377600-2379200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:2377800-2378800	Enhancers	HSMMtube	muscle
24	chr6:2377800-2379000	Weak transcription	Hela-S3	cervix
25	chr6:2377800-2380600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr6:2377800-2380600	Enhancers	Osteobl	bone
27	chr6:2377800-2381000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:2378000-2378200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr6:2378000-2378200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:2378000-2379200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links