Variant report

Variant	rs4903960
Chromosome Location	chr14:81455707-81455708
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11625251	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs2024428	0.90[CEU][hapmap];0.80[EUR][1000 genomes]
rs6574616	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7143071	0.80[EUR][1000 genomes]
rs7145701	0.80[EUR][1000 genomes]
rs726019	0.83[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81455000-81455800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr14:81455000-81455800	Enhancers	Osteobl	bone
3	chr14:81455200-81455800	Enhancers	Fetal Thymus	thymus
4	chr14:81455200-81456000	Enhancers	Primary B cells from peripheral blood	blood
5	chr14:81455400-81456200	Genic enhancers	Dnd41	blood
6	chr14:81455400-81463800	Weak transcription	Thymus	Thymus

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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