Variant report

Variant	rs8013010
Chromosome Location	chr14:81030333-81030334
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12432505	0.82[AMR][1000 genomes]
rs12434618	0.90[CEU][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17110752	0.90[CEU][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17110815	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17110880	0.80[CEU][hapmap]
rs2122429	0.82[CEU][hapmap]
rs2619671	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs58877537	0.85[AMR][1000 genomes]
rs7153490	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs7160951	0.82[CEU][hapmap]
rs72689053	0.85[AMR][1000 genomes]
rs72689058	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72689070	0.82[EUR][1000 genomes]
rs8017133	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv902116	chr14:81018237-81082400	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81028400-81033400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:81029600-81044800	Weak transcription	Dnd41	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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