Variant report

Variant	rs11710738
Chromosome Location	chr3:111481775-111481776
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10212300	0.90[ASN][1000 genomes]
rs10470303	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10934106	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10934107	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11711533	0.87[CEU][hapmap]
rs11711582	0.91[CEU][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12330761	0.92[CEU][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12490166	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12490595	0.96[ASN][1000 genomes]
rs12496925	0.96[ASN][1000 genomes]
rs12496971	0.96[ASN][1000 genomes]
rs12497012	0.87[ASN][1000 genomes]
rs13069980	0.95[ASN][1000 genomes]
rs13074817	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs13079085	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2137595	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs4284954	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs4413291	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs4431081	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4682057	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4682299	0.96[CEU][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4682303	0.92[CEU][hapmap];0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4682305	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4682312	0.92[CEU][hapmap];1.00[YRI][hapmap]
rs4682314	0.92[CEU][hapmap];1.00[YRI][hapmap]
rs56028731	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62273780	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62275532	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6438008	0.96[ASN][1000 genomes]
rs6438009	0.96[ASN][1000 genomes]
rs6764720	0.85[ASN][1000 genomes]
rs6768713	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6777540	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6784753	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6786292	0.82[AFR][1000 genomes]
rs6786386	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6786612	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6788543	0.92[CEU][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6790072	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6790079	1.00[ASN][1000 genomes]
rs6792493	0.84[ASN][1000 genomes]
rs6796087	0.92[CEU][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6802995	0.99[ASN][1000 genomes]
rs7427201	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7609653	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7614443	1.00[ASN][1000 genomes]
rs955381	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs959540	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9818574	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9823974	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9825915	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9834030	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9838371	1.00[ASN][1000 genomes]
rs9863403	1.00[ASN][1000 genomes]
rs9868171	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9868909	0.96[CEU][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9870656	0.92[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs9870823	0.95[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	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv829676	chr3:111464087-111619200	Genic enhancers Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111477400-111481800	Weak transcription	Left Ventricle	heart
2	chr3:111477600-111484600	Enhancers	HMEC	breast
3	chr3:111478000-111484600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:111478800-111484200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr3:111478800-111484200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr3:111478800-111484800	Enhancers	Rectal Smooth Muscle	rectum
7	chr3:111479200-111482600	Weak transcription	HepG2	liver
8	chr3:111479800-111483800	Enhancers	A549	lung
9	chr3:111479800-111484400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr3:111479800-111484800	Enhancers	Osteobl	bone
11	chr3:111480000-111484000	Enhancers	NH-A	brain
12	chr3:111480000-111484400	Enhancers	Colon Smooth Muscle	Colon
13	chr3:111480000-111484400	Enhancers	Hela-S3	cervix
14	chr3:111480200-111482000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:111480200-111484200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr3:111480200-111484400	Enhancers	NHLF	lung
17	chr3:111480200-111484600	Enhancers	Placenta Amnion	Placenta Amnion
18	chr3:111480200-111492000	Enhancers	Liver	Liver
19	chr3:111480400-111482200	Enhancers	Duodenum Smooth Muscle	Duodenum
20	chr3:111480400-111482200	Enhancers	Fetal Thymus	thymus
21	chr3:111480400-111482800	Enhancers	Fetal Muscle Leg	muscle
22	chr3:111480400-111483000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:111480400-111483000	Enhancers	Fetal Stomach	stomach
24	chr3:111480400-111484400	Enhancers	NHEK	skin
25	chr3:111480600-111483000	Weak transcription	Fetal Lung	lung
26	chr3:111480600-111484200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr3:111480600-111484400	Enhancers	HSMMtube	muscle
28	chr3:111480600-111484800	Enhancers	NHDF-Ad	bronchial
29	chr3:111480600-111486000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr3:111480800-111481800	Weak transcription	Stomach Mucosa	stomach
31	chr3:111480800-111482000	Enhancers	Esophagus	oesophagus
32	chr3:111480800-111483400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr3:111480800-111483400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr3:111480800-111484200	Enhancers	Stomach Smooth Muscle	stomach
35	chr3:111480800-111484400	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr3:111480800-111484400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr3:111480800-111484400	Enhancers	HSMM	muscle
38	chr3:111480800-111484600	Enhancers	Adipose Nuclei	Adipose
39	chr3:111481000-111481800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr3:111481000-111481800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr3:111481000-111481800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr3:111481000-111481800	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr3:111481000-111482800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr3:111481000-111482800	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr3:111481000-111483800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:111481000-111487400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:111481000-111487400	Weak transcription	Right Atrium	heart
48	chr3:111481200-111481800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:111481200-111482200	Enhancers	Fetal Heart	heart
50	chr3:111481400-111482600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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