Variant report

Variant	rs28719919
Chromosome Location	chr8:125127577-125127578
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10090974	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs10105799	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10107268	1.00[ASN][1000 genomes]
rs28610529	1.00[ASN][1000 genomes]
rs28616090	1.00[ASN][1000 genomes]
rs28625683	1.00[ASN][1000 genomes]
rs61354499	0.84[ASN][1000 genomes]
rs6988620	0.86[AMR][1000 genomes]
rs73332237	1.00[ASN][1000 genomes]
rs73332239	1.00[ASN][1000 genomes]
rs73332242	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv612144	chr8:125057728-125206503	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1023183	chr8:125060532-125206445	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv948556	chr8:125067187-125204721	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv831452	chr8:125099708-125259926	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 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	chr8:125119600-125129400	Enhancers	Fetal Heart	heart
2	chr8:125121800-125142000	Weak transcription	Stomach Mucosa	stomach
3	chr8:125124400-125129800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:125124600-125129800	Weak transcription	Fetal Intestine Small	intestine
5	chr8:125124800-125127600	Weak transcription	Left Ventricle	heart
6	chr8:125124800-125129800	Weak transcription	Fetal Intestine Large	intestine
7	chr8:125125000-125127600	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr8:125127200-125127800	Enhancers	Psoas Muscle	Psoas
9	chr8:125127400-125127800	Enhancers	Skeletal Muscle Male	skeletal muscle

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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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