Variant report

Variant	rs13011711
Chromosome Location	chr2:58338086-58338087
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:58337270..58338866-chr2:58352750..58354889,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1016771	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];0.95[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1051061	1.00[CEU][hapmap];0.91[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.81[LWK][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1100188	0.87[CEU][hapmap]
rs11678320	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12996679	0.80[CEU][hapmap];0.86[JPT][hapmap]
rs12999901	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2678902	0.82[MEX][hapmap]
rs2717026	0.82[MEX][hapmap]
rs2717038	0.82[MEX][hapmap]
rs2717039	0.82[MEX][hapmap]
rs35248619	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3771213	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57390191	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62140014	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6719889	0.87[YRI][hapmap]
rs7561688	0.91[MEX][hapmap]
rs848279	0.87[CEU][hapmap];0.82[MKK][hapmap];0.87[TSI][hapmap]
rs848280	0.83[CEU][hapmap];0.87[MKK][hapmap];0.85[TSI][hapmap]
rs848282	0.83[CEU][hapmap];0.82[MKK][hapmap];0.91[TSI][hapmap]
rs848291	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs848292	0.87[CEU][hapmap];0.81[TSI][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	nsv525988	chr2:58161520-58427786	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv582097	chr2:58266099-58346966	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv874201	chr2:58269871-58350504	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv874202	chr2:58269871-58375688	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv999042	chr2:58326123-58530903	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv535734	chr2:58326123-58530903	ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:58282600-58350400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr2:58303000-58358800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr2:58311200-58382400	Weak transcription	Aorta	Aorta
4	chr2:58315200-58389600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr2:58318200-58373200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr2:58319400-58358400	Weak transcription	Ovary	ovary
7	chr2:58319800-58349800	Weak transcription	Primary T cells from cord blood	blood
8	chr2:58319800-58350800	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr2:58319800-58359000	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr2:58319800-58367200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr2:58320000-58339600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr2:58320000-58347600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr2:58320000-58359000	Weak transcription	Left Ventricle	heart
14	chr2:58322200-58347400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:58322600-58349800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr2:58322600-58350400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr2:58323200-58347600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr2:58323200-58350400	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr2:58323600-58350200	Weak transcription	Liver	Liver
20	chr2:58326400-58347600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr2:58327000-58339600	Weak transcription	K562	blood
22	chr2:58327000-58347600	Weak transcription	Primary hematopoietic stem cells	blood
23	chr2:58332400-58370800	Weak transcription	Duodenum Mucosa	Duodenum
24	chr2:58333000-58341800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr2:58335200-58339400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr2:58335200-58348200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr2:58335600-58340000	Weak transcription	Stomach Mucosa	stomach
28	chr2:58335600-58347800	Weak transcription	Adipose Nuclei	Adipose
29	chr2:58335800-58339600	Weak transcription	HUVEC	blood vessel
30	chr2:58335800-58339800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr2:58335800-58339800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:58335800-58350600	Weak transcription	Brain Hippocampus Middle	brain
33	chr2:58335800-58358600	Weak transcription	Brain Anterior Caudate	brain
34	chr2:58336000-58339400	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr2:58336000-58339600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr2:58336200-58339400	Weak transcription	NHEK	skin
37	chr2:58336200-58339600	Weak transcription	HMEC	breast
38	chr2:58336200-58339800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:58336400-58339200	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr2:58336400-58339200	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr2:58336400-58339600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr2:58336400-58339600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr2:58336400-58339600	Weak transcription	NH-A	brain
44	chr2:58336400-58365000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr2:58336600-58339400	Weak transcription	Hela-S3	cervix
46	chr2:58336600-58339600	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr2:58336600-58339800	Weak transcription	Osteobl	bone
48	chr2:58336800-58339400	Genic enhancers	A549	lung
49	chr2:58336800-58339800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr2:58337000-58339800	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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