Variant report

Variant	rs73285283
Chromosome Location	chr14:70284924-70284925
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10134553	1.00[ASN][1000 genomes]
rs10151946	1.00[EUR][1000 genomes]
rs10450925	1.00[ASN][1000 genomes]
rs12896497	1.00[ASN][1000 genomes]
rs17107278	1.00[ASN][1000 genomes]
rs17107328	1.00[EUR][1000 genomes]
rs28607349	1.00[ASN][1000 genomes]
rs56203918	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57714406	1.00[EUR][1000 genomes]
rs58712157	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73283334	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73285246	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73285258	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73285287	1.00[EUR][1000 genomes]
rs73286913	1.00[EUR][1000 genomes]
rs8014019	1.00[ASN][1000 genomes]
rs9323529	1.00[ASN][1000 genomes]

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	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

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70280000-70285200	Weak transcription	Hela-S3	cervix
2	chr14:70281200-70285200	Weak transcription	HepG2	liver
3	chr14:70282400-70287800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr14:70283600-70286000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:70284200-70288200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:70284800-70285000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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Input of quick search could be:

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

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