Variant report

Variant	rs7581446
Chromosome Location	chr2:33423801-33423802
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10205739	0.82[ASN][1000 genomes]
rs10211514	0.83[EUR][1000 genomes]
rs1065324	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11124310	0.82[EUR][1000 genomes]
rs11681694	0.81[ASN][1000 genomes]
rs12104955	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12611532	0.83[EUR][1000 genomes]
rs12611549	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12617948	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12617970	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1377947	0.81[ASN][1000 genomes]
rs1454378	0.81[ASN][1000 genomes]
rs17566780	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17567417	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17641062	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17641180	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1869542	0.82[ASN][1000 genomes]
rs2061026	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2061027	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2367619	0.82[EUR][1000 genomes]
rs2367620	0.81[EUR][1000 genomes]
rs2367623	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34577456	0.82[EUR][1000 genomes]
rs4670245	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4670251	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4670252	0.82[EUR][1000 genomes]
rs4670307	0.81[ASN][1000 genomes]
rs4670778	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4670822	0.83[EUR][1000 genomes]
rs4670828	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4670833	0.83[EUR][1000 genomes]
rs4670836	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4670849	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4670857	0.82[EUR][1000 genomes]
rs4670860	0.82[EUR][1000 genomes]
rs4670863	0.82[EUR][1000 genomes]
rs4670928	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4671010	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4671024	0.82[EUR][1000 genomes]
rs5006120	0.83[EUR][1000 genomes]
rs5006124	0.80[EUR][1000 genomes]
rs5006125	0.82[EUR][1000 genomes]
rs5006126	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55911139	0.80[EUR][1000 genomes]
rs56282338	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56988251	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58774073	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58920936	0.92[ASN][1000 genomes]
rs60000782	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60558455	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62146677	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62146678	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62146679	0.82[EUR][1000 genomes]
rs62146726	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6543698	0.83[EUR][1000 genomes]
rs6543699	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6543700	0.83[EUR][1000 genomes]
rs6705772	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6707904	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6707962	0.82[EUR][1000 genomes]
rs6712473	0.83[EUR][1000 genomes]
rs6720059	0.83[EUR][1000 genomes]
rs6720185	0.83[EUR][1000 genomes]
rs6720405	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6736908	0.83[EUR][1000 genomes]
rs6748806	0.83[EUR][1000 genomes]
rs6751657	0.83[EUR][1000 genomes]
rs6759943	0.82[EUR][1000 genomes]
rs726429	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7423390	0.82[ASN][1000 genomes]
rs7580348	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7584473	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7595240	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9308931	0.82[ASN][1000 genomes]
rs964702	0.82[ASN][1000 genomes]
rs964703	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs996102	0.82[ASN][1000 genomes]
rs996103	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	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:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33403800-33489800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:33409200-33441600	Weak transcription	Psoas Muscle	Psoas
3	chr2:33410400-33438000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:33414000-33427800	Weak transcription	Right Ventricle	heart
5	chr2:33414000-33434200	Weak transcription	HUVEC	blood vessel
6	chr2:33414600-33455400	Weak transcription	Fetal Stomach	stomach
7	chr2:33415000-33434400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr2:33415200-33427600	Weak transcription	Left Ventricle	heart
9	chr2:33415200-33441600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr2:33415400-33441600	Weak transcription	Fetal Muscle Leg	muscle
11	chr2:33415600-33427000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr2:33415600-33431800	Weak transcription	NHDF-Ad	bronchial
13	chr2:33415600-33434200	Weak transcription	K562	blood
14	chr2:33415800-33431800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:33417400-33431800	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr2:33418200-33433400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr2:33418400-33435000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr2:33418800-33427000	Weak transcription	Ovary	ovary
19	chr2:33419000-33434200	Weak transcription	NH-A	brain
20	chr2:33419400-33427400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr2:33419800-33427800	Weak transcription	Aorta	Aorta
22	chr2:33420000-33432000	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr2:33420800-33430400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:33421000-33426800	Weak transcription	Osteobl	bone
25	chr2:33421000-33427400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:33421000-33427400	Weak transcription	NHLF	lung
27	chr2:33421200-33427200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:33422800-33427000	Weak transcription	Fetal Heart	heart
29	chr2:33423000-33427000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:33423000-33439400	Weak transcription	Pancreas	Pancrea
31	chr2:33423000-33439600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:33423200-33427400	Weak transcription	Liver	Liver

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