Variant report

Variant	rs10455283
Chromosome Location	chr6:74425773-74425774
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12203043	0.83[EUR][1000 genomes]
rs13201723	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1501191	0.83[EUR][1000 genomes]
rs1875367	0.85[EUR][1000 genomes]
rs2134016	0.83[EUR][1000 genomes]
rs2173853	0.83[EUR][1000 genomes]
rs35027042	0.83[EUR][1000 genomes]
rs4235875	0.83[EUR][1000 genomes]
rs4708077	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6923034	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7767106	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9293937	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9293938	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9442953	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9442956	0.83[EUR][1000 genomes]
rs9446995	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9446996	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9447001	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886158	chr6:74126084-74436825	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
2	nsv1027968	chr6:74155378-74521923	Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
3	nsv538305	chr6:74155378-74521923	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	nsv1023250	chr6:74189642-74605976	Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
5	nsv538306	chr6:74189642-74605976	Strong transcription Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
6	nsv463154	chr6:74412048-74775904	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv603695	chr6:74412048-74775904	Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74408000-74446800	Weak transcription	Dnd41	blood
2	chr6:74414800-74474600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:74415200-74432200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:74421000-74432200	Weak transcription	HSMM	muscle
5	chr6:74422600-74432000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:74423600-74441000	Weak transcription	Stomach Smooth Muscle	stomach
7	chr6:74424200-74426400	Weak transcription	Right Ventricle	heart
8	chr6:74424200-74432200	Weak transcription	Colon Smooth Muscle	Colon
9	chr6:74424200-74432600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr6:74424200-74434400	Weak transcription	Placenta	Placenta
11	chr6:74424200-74443200	Weak transcription	Right Atrium	heart
12	chr6:74424400-74426000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:74424400-74426800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr6:74424400-74431600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:74424400-74434800	Weak transcription	Adipose Nuclei	Adipose
16	chr6:74424600-74430600	Weak transcription	Fetal Heart	heart
17	chr6:74424800-74431600	Weak transcription	NHLF	lung
18	chr6:74424800-74431800	Weak transcription	NH-A	brain
19	chr6:74425000-74425800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr6:74425000-74426000	Weak transcription	Fetal Muscle Trunk	muscle
21	chr6:74425000-74427800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:74425000-74432000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:74425000-74443600	Weak transcription	Lung	lung
24	chr6:74425200-74430400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:74425200-74430400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr6:74425200-74432000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:74425200-74439800	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr6:74425200-74475800	Weak transcription	Hela-S3	cervix
29	chr6:74425400-74431800	Weak transcription	HMEC	breast
30	chr6:74425400-74432000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr6:74425400-74432000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:74425400-74432000	Weak transcription	NHEK	skin
33	chr6:74425400-74432000	Weak transcription	Osteobl	bone
34	chr6:74425400-74483200	Weak transcription	A549	lung
35	chr6:74425600-74427200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:74425600-74427200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:74425600-74428800	Weak transcription	NHDF-Ad	bronchial
38	chr6:74425600-74430000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr6:74425600-74431800	Weak transcription	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links