Variant report

Variant	rs3733961
Chromosome Location	chr5:112181283-112181284
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:112176263..112181367-chr5:112181688..112184725,5	K562	blood:
2	chr5:112089718..112092112-chr5:112180535..112183405,2	K562	blood:
3	chr5:112180772..112183270-chr5:112188278..112191041,2	K562	blood:
4	chr5:112180694..112183270-chr5:112188278..112192219,3	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10058561	0.80[ASN][1000 genomes]
rs10515446	0.91[CHB][hapmap];0.91[CHD][hapmap];0.83[GIH][hapmap];0.85[JPT][hapmap];0.89[MEX][hapmap]
rs11555908	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11950612	0.82[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs12189	1.00[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17135066	0.92[ASN][1000 genomes]
rs17135070	0.82[CHB][hapmap];0.81[CHD][hapmap];0.80[ASN][1000 genomes]
rs17135100	0.82[CHB][hapmap];0.81[CHD][hapmap]
rs17135108	0.81[CHD][hapmap]
rs17135149	0.82[CHB][hapmap];0.81[CHD][hapmap]
rs17135155	0.82[CHB][hapmap];0.81[CHD][hapmap]
rs17164132	1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap]
rs1734242	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs1804197	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2304793	1.00[ASW][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.82[GIH][hapmap];0.85[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes]
rs2707761	0.91[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2900065	0.80[ASN][1000 genomes]
rs3733963	0.82[CHB][hapmap];0.81[CHD][hapmap];0.80[ASN][1000 genomes]
rs3822652	0.80[ASN][1000 genomes]
rs3822654	0.82[CHB][hapmap];0.86[CHD][hapmap];0.80[ASN][1000 genomes]
rs58865195	0.80[ASN][1000 genomes]
rs6594652	0.82[CHB][hapmap]
rs6864403	0.82[CHB][hapmap]
rs6885768	0.83[ASN][1000 genomes]
rs6891448	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs6899169	1.00[EUR][1000 genomes]
rs7703438	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs7706623	0.82[CHB][hapmap];0.91[CHD][hapmap];0.94[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap]
rs7712157	1.00[EUR][1000 genomes]
rs7712303	1.00[EUR][1000 genomes]
rs7712537	1.00[EUR][1000 genomes]
rs7728109	0.91[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7728216	1.00[EUR][1000 genomes]
rs7728481	0.80[ASN][1000 genomes]
rs7728766	0.80[ASN][1000 genomes]
rs7729562	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7735121	0.82[CHB][hapmap]

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	nsv1032464	chr5:112076061-112192380	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
2	nsv537862	chr5:112076061-112192380	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
3	esv33290	chr5:112110808-112238295	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv1029271	chr5:112113308-112325943	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv1034239	chr5:112161239-112194693	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
6	nsv529536	chr5:112174106-112269758	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112093400-112183800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr5:112140400-112183800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:112152000-112183800	Weak transcription	Gastric	stomach
4	chr5:112155000-112183800	Weak transcription	Aorta	Aorta
5	chr5:112163400-112183800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr5:112165400-112182400	Weak transcription	Right Ventricle	heart
7	chr5:112174000-112182200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr5:112174000-112182400	Weak transcription	Esophagus	oesophagus
9	chr5:112174000-112183800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr5:112174200-112183800	Weak transcription	Hela-S3	cervix
11	chr5:112174400-112182400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr5:112174400-112183600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr5:112174600-112183800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr5:112174600-112184200	Weak transcription	Ovary	ovary
15	chr5:112174800-112183800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr5:112174800-112183800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr5:112174800-112183800	Weak transcription	NHEK	skin
18	chr5:112175200-112183800	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr5:112175400-112183800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr5:112175400-112187600	Weak transcription	NHLF	lung
21	chr5:112175600-112182200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr5:112175600-112183800	Weak transcription	Psoas Muscle	Psoas
23	chr5:112175600-112183800	Weak transcription	GM12878-XiMat	blood
24	chr5:112175600-112184000	Weak transcription	Colon Smooth Muscle	Colon
25	chr5:112175600-112184000	Weak transcription	Placenta	Placenta
26	chr5:112175800-112183600	Weak transcription	Liver	Liver
27	chr5:112175800-112183800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:112175800-112183800	Weak transcription	Duodenum Mucosa	Duodenum
29	chr5:112175800-112183800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr5:112175800-112183800	Weak transcription	A549	lung
31	chr5:112175800-112183800	Weak transcription	Dnd41	blood
32	chr5:112176000-112181600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:112176000-112183800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr5:112176000-112183800	Weak transcription	Brain Cingulate Gyrus	brain
35	chr5:112176200-112181600	Weak transcription	Fetal Heart	heart
36	chr5:112176200-112182000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr5:112176200-112182200	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr5:112176200-112182400	Weak transcription	Pancreas	Pancrea
39	chr5:112176200-112183800	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr5:112176200-112183800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr5:112176200-112183800	Weak transcription	HUVEC	blood vessel
42	chr5:112176200-112183800	Weak transcription	NH-A	brain
43	chr5:112176200-112183800	Weak transcription	Osteobl	bone
44	chr5:112176200-112184000	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr5:112176400-112182200	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr5:112176400-112182200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr5:112176400-112182400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr5:112176400-112183600	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr5:112176400-112183800	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr5:112176400-112183800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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