Variant report

Variant	rs4899784
Chromosome Location	chr14:81487500-81487501
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10873332	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12436366	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2268466	0.87[ASN][1000 genomes]
rs34146411	0.84[EUR][1000 genomes]
rs4903965	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4903967	0.94[ASN][1000 genomes]
rs59484155	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72689907	0.87[ASN][1000 genomes]
rs72689910	0.87[ASN][1000 genomes]
rs72695035	0.87[ASN][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	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	nsv1052999	chr14:81468860-81599074	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv542144	chr14:81468860-81599074	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81455800-81492200	Weak transcription	Fetal Thymus	thymus
2	chr14:81484600-81502400	Weak transcription	Liver	Liver
3	chr14:81486800-81487800	Enhancers	K562	blood
4	chr14:81487000-81489600	Weak transcription	Dnd41	blood
5	chr14:81487000-81498600	Weak transcription	Thymus	Thymus

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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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