Variant report

Variant	rs12450787
Chromosome Location	chr17:66794003-66794004
allele	G/T
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:16)

rs_ID	r²[population]
rs11650010	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11657619	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12452140	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35131140	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35295565	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4968953	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4968955	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4968956	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4968957	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55982272	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9302983	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9894084	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9894119	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9898028	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9902321	0.90[EUR][1000 genomes]
rs9905519	0.96[EUR][1000 genomes];0.94[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	nsv1067334	chr17:66695039-67221585	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv543411	chr17:66695039-67221585	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv575927	chr17:66787428-66817866	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66788000-66805800	Weak transcription	Right Atrium	heart
2	chr17:66791600-66796800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr17:66791600-66797800	Weak transcription	Ovary	ovary
4	chr17:66791800-66796600	Weak transcription	Osteobl	bone
5	chr17:66791800-66796800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr17:66791800-66796800	Weak transcription	NHDF-Ad	bronchial
7	chr17:66791800-66797000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr17:66792400-66798000	Weak transcription	Fetal Muscle Leg	muscle
9	chr17:66792600-66803200	Weak transcription	HepG2	liver
10	chr17:66793200-66796600	Weak transcription	Adipose Nuclei	Adipose
11	chr17:66793800-66799400	Weak transcription	Brain Hippocampus Middle	brain

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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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