Variant report

Variant	rs7604033
Chromosome Location	chr2:179626017-179626018
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	chr2:179625849..179626645-chr2:179778697..179779282,2	MCF-7	breast:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10171049	0.86[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11895382	0.86[ASW][hapmap];0.84[GIH][hapmap];0.87[LWK][hapmap];0.83[AFR][1000 genomes]
rs11902709	0.80[CHB][hapmap]
rs12464703	0.86[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs12465449	0.81[AMR][1000 genomes]
rs12470905	0.87[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs12476289	0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs13421990	0.81[GIH][hapmap]
rs16866497	0.87[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs16866532	0.87[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs1883085	0.80[CHB][hapmap]
rs2054708	1.00[CEU][hapmap];0.85[GIH][hapmap];0.87[TSI][hapmap];0.89[EUR][1000 genomes]
rs2243804	0.80[CHB][hapmap]
rs2255480	0.80[CHB][hapmap]
rs2291304	0.87[CHB][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs2291305	0.90[ASN][1000 genomes]
rs2291308	0.87[CHB][hapmap];0.83[CHD][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs2291309	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2291310	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2291311	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2291312	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2306636	0.87[CHB][hapmap];0.83[CHD][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs2562829	0.80[CHB][hapmap]
rs2562832	0.80[CHB][hapmap]
rs2562835	0.80[CHB][hapmap]
rs2562837	0.80[CHB][hapmap]
rs2562841	0.80[CHB][hapmap]
rs2562852	0.80[CHB][hapmap]
rs2562853	0.80[CHB][hapmap]
rs2562854	0.83[CHB][hapmap]
rs2627037	0.89[CEU][hapmap];0.80[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];0.87[TSI][hapmap];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2627040	0.80[CHB][hapmap]
rs2627042	0.80[CHB][hapmap];0.88[CHD][hapmap];0.82[GIH][hapmap]
rs2627044	0.80[CHB][hapmap]
rs2742328	0.80[CHB][hapmap]
rs2742329	0.80[CHB][hapmap]
rs2742330	0.80[CHB][hapmap]
rs2742332	0.80[CHB][hapmap]
rs2742333	0.80[CHB][hapmap]
rs2742334	0.80[CHB][hapmap]
rs2742335	0.80[CHB][hapmap]
rs2742336	0.80[CHB][hapmap]
rs2742337	0.80[CHB][hapmap]
rs2742339	0.80[CHB][hapmap]
rs2742340	0.80[CHB][hapmap]
rs2742343	0.80[CHB][hapmap]
rs2742344	0.80[CHB][hapmap]
rs2742345	0.80[CHB][hapmap];0.88[CHD][hapmap]
rs2742347	0.80[CHB][hapmap]
rs2742357	0.80[CHB][hapmap]
rs3754953	1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4893853	0.84[GIH][hapmap];0.87[LWK][hapmap]
rs4894037	0.86[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4894048	0.81[GIH][hapmap]
rs55863869	0.89[ASN][1000 genomes]
rs56120016	0.85[ASN][1000 genomes]
rs56142888	0.89[ASN][1000 genomes]
rs66677602	0.85[ASN][1000 genomes]
rs72647889	0.92[ASN][1000 genomes]
rs72648917	0.85[ASN][1000 genomes]
rs7423101	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs7585334	1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs922984	1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834470	chr2:179555152-179728726	Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv934108	chr2:179556852-179729925	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr2:179483200-179655400	Weak transcription	Adipose Nuclei	Adipose
2	chr2:179533600-179669200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr2:179577800-179640800	Weak transcription	Fetal Intestine Large	intestine
4	chr2:179590800-179640400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr2:179605400-179662400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:179610800-179671400	Weak transcription	Ovary	ovary
7	chr2:179614200-179626400	Strong transcription	Primary T cells from cord blood	blood
8	chr2:179614200-179645200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr2:179614400-179632400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr2:179614800-179626600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr2:179614800-179628800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr2:179617200-179627800	Weak transcription	Psoas Muscle	Psoas
13	chr2:179618600-179626600	Genic enhancers	Fetal Heart	heart
14	chr2:179619000-179636000	Strong transcription	Left Ventricle	heart
15	chr2:179619200-179630400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr2:179620600-179634400	Weak transcription	Brain Anterior Caudate	brain
17	chr2:179621800-179629200	Weak transcription	Right Ventricle	heart
18	chr2:179622200-179628800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr2:179622400-179626400	Weak transcription	HSMM	muscle
20	chr2:179622600-179628800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:179622600-179628800	Strong transcription	HSMMtube	muscle
22	chr2:179622600-179640600	Weak transcription	Pancreas	Pancrea
23	chr2:179622800-179626200	Weak transcription	NHDF-Ad	bronchial
24	chr2:179622800-179630000	Weak transcription	Primary B cells from peripheral blood	blood
25	chr2:179623800-179631200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr2:179624000-179629000	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr2:179624200-179627600	Weak transcription	Primary B cells from cord blood	blood
28	chr2:179624400-179627600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr2:179625200-179626800	Strong transcription	Fetal Muscle Trunk	muscle
30	chr2:179625200-179627600	Strong transcription	Fetal Muscle Leg	muscle
31	chr2:179625800-179628000	Strong transcription	Skeletal Muscle Female	skeletal muscle
32	chr2:179625800-179629200	Strong transcription	Skeletal Muscle Male	skeletal muscle

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