Variant report

Variant	rs28673055
Chromosome Location	chr3:118632075-118632076
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs28440859	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28484956	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28565574	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28573387	0.91[AFR][1000 genomes]
rs28655404	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6779428	0.91[AFR][1000 genomes]
rs6795721	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72966895	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968613	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968638	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968654	0.80[AFR][1000 genomes]
rs9809027	0.83[AMR][1000 genomes]
rs9811829	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9828087	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9841148	0.80[AFR][1000 genomes]
rs9849421	0.88[AFR][1000 genomes];1.00[AMR][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	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118619800-118651400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr3:118620200-118663200	Weak transcription	Pancreas	Pancrea
3	chr3:118622000-118644600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:118625400-118639800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr3:118627600-118632400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr3:118627800-118632600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:118627800-118632600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr3:118627800-118642200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr3:118630000-118641600	Weak transcription	Brain Angular Gyrus	brain
10	chr3:118631200-118632400	Weak transcription	K562	blood
11	chr3:118631600-118632600	Weak transcription	Brain Hippocampus Middle	brain
12	chr3:118631800-118639600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr3:118631800-118639600	Weak transcription	Ovary	ovary

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

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