Variant report

Variant	rs36093037
Chromosome Location	chr14:81455306-81455307
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12184983	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12880945	0.83[EUR][1000 genomes]
rs12881268	0.83[EUR][1000 genomes]
rs12883673	0.83[EUR][1000 genomes]
rs12890676	0.83[EUR][1000 genomes]
rs17111361	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34074777	0.83[EUR][1000 genomes]
rs34277709	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35336887	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35523135	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35554250	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35789100	0.81[EUR][1000 genomes]
rs71416856	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]

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:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81451000-81455400	Enhancers	Dnd41	blood
2	chr14:81453400-81455600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr14:81454600-81455400	Enhancers	Thymus	Thymus
4	chr14:81455000-81455600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr14:81455000-81455600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr14:81455000-81455800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr14:81455000-81455800	Enhancers	Osteobl	bone
8	chr14:81455200-81455800	Enhancers	Fetal Thymus	thymus
9	chr14:81455200-81456000	Enhancers	Primary B cells from peripheral blood	blood

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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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