Variant report

Variant	rs8015375
Chromosome Location	chr14:106135632-106135633
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10144746	0.82[EUR][1000 genomes]
rs10146949	0.82[EUR][1000 genomes]
rs12884681	0.81[CHB][hapmap];0.85[CHD][hapmap]
rs2516747	0.89[EUR][1000 genomes]
rs2516751	0.90[EUR][1000 genomes]
rs2516752	0.90[EUR][1000 genomes]
rs2516755	0.89[EUR][1000 genomes]
rs2855788	0.88[EUR][1000 genomes]
rs34678053	0.90[EUR][1000 genomes]
rs61984791	0.81[EUR][1000 genomes]
rs7154333	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][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	nsv530813	chr14:105607701-106453697	Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8015375	IGHJ6	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:106130600-106136000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:106131400-106137000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr14:106135600-106142000	Weak transcription	Primary B cells from peripheral blood	blood

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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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