Variant report

Variant	rs10146035
Chromosome Location	chr14:84771848-84771849
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10134005	0.92[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10137608	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10150745	0.85[EUR][1000 genomes]
rs17119896	0.91[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs28399118	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs28446157	0.85[EUR][1000 genomes]
rs3935697	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4075208	0.97[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4277283	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7142508	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7143199	0.95[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs7148565	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs8005901	0.85[EUR][1000 genomes]
rs8009583	0.89[AFR][1000 genomes];0.85[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	nsv832845	chr14:84726378-84900199	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84769800-84772600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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