Variant report

Variant	rs4475303
Chromosome Location	chr6:163702711-163702712
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12174929	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12525217	0.95[AFR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1534939	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2874545	0.84[EUR][1000 genomes]
rs4470828	0.84[EUR][1000 genomes]
rs4576225	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4579329	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4708985	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4709688	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62428011	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7750165	0.82[EUR][1000 genomes]
rs7760002	0.82[YRI][hapmap]
rs7770851	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9365546	0.84[AFR][1000 genomes];0.84[EUR][1000 genomes];0.84[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	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1026490	chr6:163133433-163705708	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1022610	chr6:163591786-163814041	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv605188	chr6:163697439-163772096	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163686000-163706000	Weak transcription	Brain Angular Gyrus	brain
2	chr6:163701400-163705800	Weak transcription	Brain Anterior Caudate	brain
3	chr6:163701600-163705200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr6:163701800-163731200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:163702200-163702800	Enhancers	Placenta	Placenta
6	chr6:163702200-163703400	Enhancers	HUVEC	blood vessel
7	chr6:163702400-163705200	Weak transcription	Left Ventricle	heart
8	chr6:163702400-163710000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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