Variant report

Variant	rs4981995
Chromosome Location	chr14:33111168-33111169
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10130459	0.88[CHB][hapmap];0.82[JPT][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10135053	0.88[CHB][hapmap];0.82[JPT][hapmap];0.97[ASN][1000 genomes]
rs10138218	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1033678	0.88[CHB][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11625087	0.88[CHB][hapmap];0.82[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12717222	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12896132	0.81[ASN][1000 genomes]
rs1884618	0.94[ASN][1000 genomes]
rs1956203	0.92[ASN][1000 genomes]
rs1956219	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3784203	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4981993	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6571547	0.88[CHB][hapmap];0.82[JPT][hapmap];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6571548	0.88[CHB][hapmap];0.92[ASN][1000 genomes]
rs7146517	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7152044	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7153048	0.82[JPT][hapmap];0.97[ASN][1000 genomes]
rs7154753	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7156763	0.88[CHB][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7157328	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7157533	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7157744	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7160156	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs927060	0.88[CHB][hapmap];0.83[AMR][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	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

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:33099200-33120400	Weak transcription	Fetal Muscle Leg	muscle
2	chr14:33103200-33114600	Weak transcription	Aorta	Aorta
3	chr14:33104600-33120400	Weak transcription	HSMMtube	muscle
4	chr14:33104800-33116400	Weak transcription	Brain Substantia Nigra	brain
5	chr14:33105000-33117000	Weak transcription	Brain Cingulate Gyrus	brain
6	chr14:33105000-33117200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr14:33105200-33116000	Weak transcription	Brain Hippocampus Middle	brain
8	chr14:33105200-33116400	Weak transcription	Brain Angular Gyrus	brain
9	chr14:33107000-33130600	Weak transcription	Left Ventricle	heart
10	chr14:33107800-33113000	Weak transcription	Fetal Heart	heart
11	chr14:33110400-33116600	Weak transcription	NHDF-Ad	bronchial

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