Variant report

Variant	rs73286913
Chromosome Location	chr14:70306977-70306978
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:12)

rs_ID	r²[population]
rs10151946	1.00[EUR][1000 genomes]
rs17107328	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56203918	1.00[EUR][1000 genomes]
rs57714406	1.00[EUR][1000 genomes]
rs58194983	1.00[ASN][1000 genomes]
rs58712157	1.00[EUR][1000 genomes]
rs59938875	1.00[ASN][1000 genomes]
rs73283334	1.00[EUR][1000 genomes]
rs73285246	1.00[EUR][1000 genomes]
rs73285258	1.00[EUR][1000 genomes]
rs73285283	1.00[EUR][1000 genomes]
rs73285287	1.00[EUR][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	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
3	esv3440726	chr14:70304199-70308597	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70306400-70311200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:70306600-70307800	Enhancers	Brain Germinal Matrix	brain
3	chr14:70306600-70308200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr14:70306600-70310600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr14:70306800-70308400	Enhancers	HepG2	liver

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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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