Variant report

Variant	rs8019870
Chromosome Location	chr14:63420403-63420404
allele	A/T
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:12)

rs_ID	r²[population]
rs17100517	0.86[YRI][hapmap]
rs17100522	0.91[YRI][hapmap]
rs17100528	0.87[YRI][hapmap]
rs17100551	0.95[YRI][hapmap];0.89[AMR][1000 genomes]
rs17100561	0.86[YRI][hapmap];0.89[AMR][1000 genomes]
rs17100564	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17100566	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58900215	0.89[AMR][1000 genomes]
rs7157114	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73276489	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8018130	0.83[YRI][hapmap];0.89[AMR][1000 genomes]
rs8019319	0.91[YRI][hapmap];0.89[AMR][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	nsv527251	chr14:63400786-64068806	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv902016	chr14:63411610-63439033	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63402800-63422600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:63414600-63422800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:63419600-63422400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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