Variant report

Variant	rs4894049
Chromosome Location	chr2:179639498-179639499
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10497522	0.90[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10497524	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10497525	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11884172	0.80[YRI][hapmap];0.91[AFR][1000 genomes]
rs11887915	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11892354	0.94[ASN][1000 genomes]
rs11897386	0.88[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11904138	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12693168	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1552280	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1872202	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1905521	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2029396	0.86[EUR][1000 genomes]
rs2035496	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2046778	0.90[CHB][hapmap]
rs2054706	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2054707	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2291301	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2291302	0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2291303	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303836	0.85[JPT][hapmap]
rs2306637	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3754949	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3754950	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3769859	0.90[CHB][hapmap];0.93[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3769861	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3769862	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3816781	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58025762	0.86[EUR][1000 genomes]
rs58152091	1.00[ASN][1000 genomes]
rs60305852	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61680869	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs719201	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72648911	0.81[AFR][1000 genomes]
rs72648915	0.91[AFR][1000 genomes]
rs73973151	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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
3	nsv962089	chr2:179635536-179643793	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:43 , 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	chr2:179614200-179645200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr2:179622600-179640600	Weak transcription	Pancreas	Pancrea
9	chr2:179627000-179655200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:179627400-179653200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr2:179627600-179652600	Weak transcription	Brain Substantia Nigra	brain
12	chr2:179627600-179663800	Weak transcription	Thymus	Thymus
13	chr2:179629600-179666200	Weak transcription	GM12878-XiMat	blood
14	chr2:179630600-179651000	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr2:179630800-179640800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr2:179631200-179649800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:179632000-179658800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr2:179632400-179667800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr2:179632800-179641000	Weak transcription	Fetal Thymus	thymus
20	chr2:179634200-179648600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr2:179634400-179645200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr2:179635200-179640800	Weak transcription	Primary hematopoietic stem cells	blood
23	chr2:179635600-179640800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr2:179635600-179640800	Weak transcription	Fetal Muscle Trunk	muscle
25	chr2:179635800-179640800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr2:179636200-179641000	Weak transcription	Right Ventricle	heart
27	chr2:179636200-179643000	Weak transcription	HSMM	muscle
28	chr2:179636200-179647000	Weak transcription	Lung	lung
29	chr2:179636200-179660600	Weak transcription	Brain Anterior Caudate	brain
30	chr2:179637200-179639600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
31	chr2:179637200-179651000	Strong transcription	Primary T cells from cord blood	blood
32	chr2:179637200-179651000	Strong transcription	HSMMtube	muscle
33	chr2:179637400-179641400	Genic enhancers	Fetal Heart	heart
34	chr2:179637400-179643800	Strong transcription	Primary B cells from cord blood	blood
35	chr2:179637600-179640200	Strong transcription	Left Ventricle	heart
36	chr2:179637600-179641200	Strong transcription	Psoas Muscle	Psoas
37	chr2:179637600-179647000	Strong transcription	Fetal Muscle Leg	muscle
38	chr2:179639000-179672000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr2:179639200-179639600	Genic enhancers	Skeletal Muscle Female	skeletal muscle
40	chr2:179639200-179640000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr2:179639200-179640600	Weak transcription	Primary B cells from peripheral blood	blood
42	chr2:179639400-179640200	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr2:179639400-179671400	Weak transcription	Gastric	stomach

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