Variant report

Variant	rs4474865
Chromosome Location	chr2:33385073-33385074
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:33383408..33387314-chr2:33391651..33394582,3	K562	blood:
2	chr2:33382825..33385246-chr2:33385612..33388538,2	K562	blood:

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10211514	0.81[EUR][1000 genomes]
rs10432657	0.89[CEU][hapmap]
rs1065324	0.96[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12104955	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12611532	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs12611549	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12617948	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12617970	0.96[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12620853	0.96[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17565877	0.96[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17566780	0.92[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17567417	0.88[CEU][hapmap];0.80[CHB][hapmap];0.82[JPT][hapmap]
rs17568051	0.93[CEU][hapmap];0.81[CHB][hapmap];0.83[JPT][hapmap]
rs17641062	0.96[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17641180	0.96[CEU][hapmap];0.87[JPT][hapmap];0.82[EUR][1000 genomes]
rs17641906	0.92[CEU][hapmap];0.82[JPT][hapmap]
rs17642074	0.84[CEU][hapmap];0.82[JPT][hapmap]
rs1947444	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2061026	0.82[CEU][hapmap]
rs2061027	0.96[CEU][hapmap];0.83[JPT][hapmap];0.83[EUR][1000 genomes]
rs2290448	0.84[CEU][hapmap];0.80[CHB][hapmap];0.82[JPT][hapmap]
rs2367619	0.80[EUR][1000 genomes]
rs2367623	0.88[CEU][hapmap];0.82[JPT][hapmap]
rs34577456	0.81[EUR][1000 genomes]
rs4630744	0.81[CEU][hapmap]
rs4670186	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4670245	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4670251	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4670252	0.80[EUR][1000 genomes]
rs4670660	0.80[ASN][1000 genomes]
rs4670778	0.96[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4670822	0.81[EUR][1000 genomes]
rs4670828	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4670833	0.81[EUR][1000 genomes]
rs4670836	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4670849	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4670857	0.82[CHB][hapmap];0.80[EUR][1000 genomes]
rs4670860	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs4670863	0.80[EUR][1000 genomes]
rs4670928	0.96[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4671010	0.96[CEU][hapmap];0.83[JPT][hapmap];0.83[EUR][1000 genomes]
rs4671024	0.85[CEU][hapmap];0.81[CHB][hapmap];0.83[JPT][hapmap]
rs4671035	0.85[CEU][hapmap];0.83[JPT][hapmap]
rs5006120	0.81[EUR][1000 genomes]
rs5006126	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55673259	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55911139	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56282338	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56988251	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs60000782	0.82[EUR][1000 genomes]
rs60692621	0.87[ASN][1000 genomes]
rs62133341	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62146677	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62146678	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62146679	0.80[EUR][1000 genomes]
rs62146726	0.83[EUR][1000 genomes]
rs6543698	0.82[CEU][hapmap];0.82[JPT][hapmap];0.81[EUR][1000 genomes]
rs6543699	0.93[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6543700	0.81[EUR][1000 genomes]
rs6705772	0.96[CEU][hapmap];0.83[JPT][hapmap];0.83[EUR][1000 genomes]
rs6707904	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6707962	0.81[CEU][hapmap]
rs6712473	0.81[CEU][hapmap];0.80[EUR][1000 genomes]
rs6715793	0.96[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6720059	0.81[EUR][1000 genomes]
rs6720185	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs6720405	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6728094	0.89[CEU][hapmap];0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs6736908	0.81[EUR][1000 genomes]
rs6743685	0.86[CEU][hapmap];0.88[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6748806	0.81[EUR][1000 genomes]
rs6751657	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs6759943	0.80[EUR][1000 genomes]
rs726429	0.96[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7580348	0.96[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs7584473	0.80[EUR][1000 genomes]
rs7595240	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs996103	0.88[CEU][hapmap];0.82[JPT][hapmap]

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	nsv998167	chr2:33074313-33541100	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv535623	chr2:33074313-33541100	Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1005435	chr2:33136117-33747159	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
4	nsv535624	chr2:33136117-33747159	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
5	esv33628	chr2:33257484-33455355	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv873789	chr2:33297967-33390188	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv873790	chr2:33369582-33466483	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33360200-33385800	Weak transcription	Placenta	Placenta
2	chr2:33369600-33389800	Weak transcription	Right Atrium	heart
3	chr2:33369800-33404000	Weak transcription	Right Ventricle	heart
4	chr2:33371600-33395600	Weak transcription	Psoas Muscle	Psoas
5	chr2:33375000-33408400	Weak transcription	Fetal Muscle Leg	muscle
6	chr2:33382000-33386200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:33382800-33385400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr2:33383000-33385400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:33383400-33385200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:33384000-33385400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr2:33384200-33385800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr2:33384200-33386600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:33384400-33385800	Weak transcription	Aorta	Aorta
14	chr2:33384400-33386000	Enhancers	Osteobl	bone
15	chr2:33384400-33386200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr2:33384400-33386200	Enhancers	NH-A	brain
17	chr2:33384400-33386200	Enhancers	NHLF	lung
18	chr2:33384400-33391800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:33384400-33391800	Weak transcription	Ovary	ovary
20	chr2:33384400-33392000	Weak transcription	Left Ventricle	heart
21	chr2:33384600-33390800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr2:33384800-33385200	Weak transcription	NHDF-Ad	bronchial
23	chr2:33384800-33385400	Weak transcription	Fetal Heart	heart
24	chr2:33384800-33387800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr2:33384800-33390200	Weak transcription	HUVEC	blood vessel
26	chr2:33384800-33392400	Weak transcription	Stomach Smooth Muscle	stomach
27	chr2:33385000-33385400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr2:33385000-33389800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links