Variant report

Variant	rs7153041
Chromosome Location	chr14:33107318-33107319
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10129321	0.82[CEU][hapmap];0.81[AMR][1000 genomes]
rs10135558	0.83[AMR][1000 genomes]
rs10139885	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10139992	0.81[AMR][1000 genomes]
rs10140278	0.86[CEU][hapmap]
rs10143113	0.85[CEU][hapmap];0.83[AMR][1000 genomes]
rs11626506	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11627076	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11627566	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11627900	0.85[CEU][hapmap];0.82[AMR][1000 genomes]
rs12147120	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12433067	0.81[CEU][hapmap];0.82[AMR][1000 genomes]
rs12437429	0.81[AMR][1000 genomes]
rs12586675	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12586676	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12888621	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1956201	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1956220	0.95[CEU][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2180449	0.82[CEU][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7152377	0.95[CEU][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7154943	0.95[CEU][hapmap];0.88[EUR][1000 genomes]
rs7159519	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7160301	0.85[CEU][hapmap];0.82[AMR][1000 genomes]
rs8016257	0.95[CEU][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8021432	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs983766	0.95[CEU][hapmap];0.87[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045035	chr14:32986003-33543227	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv542021	chr14:32986003-33543227	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv428624	chr14:33065571-33214223	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv826913	chr14:33106831-33107529	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:33099200-33120400	Weak transcription	Fetal Muscle Leg	muscle
2	chr14:33101800-33107600	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr14:33102600-33107800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr14:33103200-33107800	Enhancers	Fetal Heart	heart
5	chr14:33103200-33114600	Weak transcription	Aorta	Aorta
6	chr14:33104600-33120400	Weak transcription	HSMMtube	muscle
7	chr14:33104800-33116400	Weak transcription	Brain Substantia Nigra	brain
8	chr14:33105000-33117000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr14:33105000-33117200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr14:33105200-33116000	Weak transcription	Brain Hippocampus Middle	brain
11	chr14:33105200-33116400	Weak transcription	Brain Angular Gyrus	brain
12	chr14:33106600-33107400	Enhancers	Right Atrium	heart
13	chr14:33106800-33107600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr14:33106800-33107600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr14:33106800-33107600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:33107000-33107400	Enhancers	Brain Anterior Caudate	brain
17	chr14:33107000-33107400	Enhancers	NH-A	brain
18	chr14:33107000-33107600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr14:33107000-33107600	Enhancers	NHDF-Ad	bronchial
20	chr14:33107000-33130600	Weak transcription	Left Ventricle	heart
21	chr14:33107200-33107400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr14:33107200-33107600	Enhancers	Osteobl	bone

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