Variant report

Variant	rs825144
Chromosome Location	chr1:223596937-223596938
allele	A/T
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]
rs1619161	0.88[ASN][1000 genomes]
rs1713213	0.88[ASN][1000 genomes]
rs1772288	0.88[ASN][1000 genomes]
rs1772289	0.88[ASN][1000 genomes]
rs1819706	0.83[ASN][1000 genomes]
rs2678369	0.88[ASN][1000 genomes]
rs2678370	0.88[ASN][1000 genomes]
rs825136	0.88[ASN][1000 genomes]
rs825137	0.88[ASN][1000 genomes]
rs825141	0.80[ASN][1000 genomes]
rs825142	0.83[ASN][1000 genomes]
rs825143	0.83[ASN][1000 genomes]
rs825145	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs825146	0.90[ASN][1000 genomes]
rs825148	0.88[ASN][1000 genomes]
rs866637	0.91[ASN][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	nsv832670	chr1:223561771-223683381	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv4687	chr1:223565080-223610362	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223592600-223597400	Weak transcription	Right Ventricle	heart
2	chr1:223594600-223597800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:223594800-223600600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:223595000-223597000	Weak transcription	Left Ventricle	heart
5	chr1:223595000-223597000	Weak transcription	Ovary	ovary
6	chr1:223595200-223597000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:223595200-223597200	Weak transcription	Fetal Heart	heart
8	chr1:223595200-223599000	Weak transcription	Esophagus	oesophagus
9	chr1:223595200-223609200	Weak transcription	Right Atrium	heart
10	chr1:223595600-223597000	Weak transcription	HMEC	breast
11	chr1:223595800-223597000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:223595800-223597000	Weak transcription	NHEK	skin
13	chr1:223596000-223597000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:223596200-223597800	Enhancers	HSMMtube	muscle
15	chr1:223596400-223597200	Enhancers	Pancreas	Pancrea
16	chr1:223596400-223597400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:223596400-223598400	Enhancers	HSMM	muscle
18	chr1:223596400-223599800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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