Variant report

Variant	rs61736814
Chromosome Location	chr10:97338433-97338434
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11188367	1.00[EUR][1000 genomes]
rs11188378	0.90[EUR][1000 genomes]
rs11188382	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11188383	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11188388	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11188391	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11188405	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11188410	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11188412	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11188413	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11188415	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11188419	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11188424	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11188431	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11188448	0.80[EUR][1000 genomes]
rs11188450	0.80[EUR][1000 genomes]
rs11188451	0.80[EUR][1000 genomes]
rs11188461	0.85[EUR][1000 genomes]
rs11188466	0.80[EUR][1000 genomes]
rs11188467	0.80[EUR][1000 genomes]
rs11188469	0.80[EUR][1000 genomes]
rs11188475	0.80[EUR][1000 genomes]
rs11553577	0.80[EUR][1000 genomes]
rs12354465	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12357211	0.85[EUR][1000 genomes]
rs12357513	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12358517	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3818833	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs41291576	0.80[EUR][1000 genomes]
rs55846129	1.00[AFR][1000 genomes]
rs56747025	0.80[EUR][1000 genomes]
rs58059905	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61587319	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7090630	0.80[EUR][1000 genomes]
rs73329287	0.80[EUR][1000 genomes]
rs73331134	0.80[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526180	chr10:97332195-97511037	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97334800-97339400	Weak transcription	Right Atrium	heart
2	chr10:97334800-97339600	Weak transcription	Left Ventricle	heart
3	chr10:97335000-97339000	Weak transcription	Aorta	Aorta
4	chr10:97335200-97373400	Weak transcription	Psoas Muscle	Psoas
5	chr10:97335600-97340800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr10:97338400-97339600	Enhancers	HSMMtube	muscle

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