Variant report

Variant	rs35351510
Chromosome Location	chr5:79578246-79578247
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs13153456	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13172073	1.00[AFR][1000 genomes]
rs13175768	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs13179394	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13179638	0.81[EUR][1000 genomes]
rs13181284	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13182247	1.00[AFR][1000 genomes]
rs13186162	1.00[AFR][1000 genomes]
rs13188642	0.81[EUR][1000 genomes]
rs13190128	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13190586	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17260885	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34006305	0.81[EUR][1000 genomes]
rs34286825	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34324791	1.00[AFR][1000 genomes]
rs34325845	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34445888	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34700139	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35098852	1.00[AFR][1000 genomes]
rs35155855	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35162143	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35187099	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35271976	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35327965	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35375564	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35606070	1.00[AFR][1000 genomes]
rs35720953	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35762887	0.81[EUR][1000 genomes]
rs35860790	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35885173	1.00[AFR][1000 genomes]
rs71636213	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs71636215	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][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	nsv948807	chr5:79549207-79805765	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv522634	chr5:79577760-79580818	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv964902	chr5:79578051-79585364	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79567800-79580400	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr5:79577800-79578600	Enhancers	Left Ventricle	heart
3	chr5:79577800-79578600	Enhancers	Right Atrium	heart
4	chr5:79577800-79578800	Enhancers	Fetal Intestine Large	intestine
5	chr5:79578200-79580600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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