Variant report

Variant	rs16866260
Chromosome Location	chr2:179198946-179198947
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs12471986	1.00[CHB][hapmap]
rs12479027	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs12618595	1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs1368903	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1368907	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1434081	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16866263	1.00[CEU][hapmap];1.00[JPT][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]
rs16866274	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16866276	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1821412	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1836205	1.00[ASN][1000 genomes]
rs2366164	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs334595	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs334596	1.00[CHB][hapmap]
rs334597	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs334601	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs334605	1.00[JPT][hapmap]
rs334607	1.00[CHB][hapmap]
rs334609	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs35032920	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4894007	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs55633450	1.00[ASN][1000 genomes]
rs55981329	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6433718	1.00[CHB][hapmap]
rs6433719	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6725937	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs731845	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7585689	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];1.00[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	nsv1009312	chr2:178924318-179215566	Weak transcription Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv536057	chr2:178924318-179215566	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv834466	chr2:179140792-179284778	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179164600-179200800	Weak transcription	Aorta	Aorta
2	chr2:179183800-179247800	Weak transcription	Psoas Muscle	Psoas
3	chr2:179189200-179201200	Weak transcription	Ovary	ovary
4	chr2:179189400-179201200	Weak transcription	Fetal Brain Male	brain
5	chr2:179189800-179217000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr2:179192600-179200600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr2:179193000-179201400	Weak transcription	NH-A	brain
8	chr2:179193000-179201800	Weak transcription	Fetal Kidney	kidney
9	chr2:179193000-179214600	Weak transcription	Fetal Intestine Large	intestine
10	chr2:179193200-179199800	Enhancers	HSMMtube	muscle
11	chr2:179193200-179201000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr2:179193200-179201400	Weak transcription	Fetal Brain Female	brain
13	chr2:179193200-179210400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:179193200-179216200	Weak transcription	Adipose Nuclei	Adipose
15	chr2:179193400-179203400	Weak transcription	Fetal Intestine Small	intestine
16	chr2:179193400-179204800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:179193400-179215000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:179194600-179229400	Weak transcription	K562	blood
19	chr2:179195000-179199200	Enhancers	HSMM	muscle
20	chr2:179195400-179214600	Weak transcription	Left Ventricle	heart
21	chr2:179195400-179229000	Weak transcription	Brain Substantia Nigra	brain
22	chr2:179195600-179214200	Weak transcription	Brain Hippocampus Middle	brain
23	chr2:179195600-179214800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr2:179196000-179201000	Weak transcription	Brain Anterior Caudate	brain
25	chr2:179196200-179207000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr2:179196400-179201200	Weak transcription	Brain Germinal Matrix	brain
27	chr2:179196600-179201000	Weak transcription	Brain Angular Gyrus	brain
28	chr2:179196600-179204600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:179196600-179213600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:179197000-179200000	Weak transcription	HMEC	breast
31	chr2:179197000-179200800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr2:179197000-179201000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:179197000-179201000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr2:179197000-179209000	Weak transcription	Esophagus	oesophagus
35	chr2:179197200-179201000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr2:179197200-179201000	Weak transcription	Gastric	stomach
37	chr2:179197800-179200600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:179197800-179201200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr2:179197800-179204200	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr2:179198000-179199600	Strong transcription	Cortex derived primary cultured neurospheres	brain
41	chr2:179198200-179199000	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr2:179198200-179199000	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr2:179198200-179199200	Enhancers	Liver	Liver
44	chr2:179198200-179199200	Enhancers	Fetal Lung	lung
45	chr2:179198400-179199000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr2:179198400-179199200	Enhancers	HepG2	liver
47	chr2:179198400-179227400	Weak transcription	NHEK	skin
48	chr2:179198600-179199000	Enhancers	Fetal Heart	heart
49	chr2:179198600-179199200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:179198800-179199000	Genic enhancers	Fetal Muscle Leg	muscle

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