Variant report

Variant	rs73782226
Chromosome Location	chr5:113731574-113731575
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10060646	0.85[ASN][1000 genomes]
rs1457764	0.85[ASN][1000 genomes]
rs1840983	0.85[ASN][1000 genomes]
rs55697384	0.85[ASN][1000 genomes]
rs55914631	0.85[ASN][1000 genomes]
rs55941350	0.85[ASN][1000 genomes]
rs56088944	0.85[ASN][1000 genomes]
rs56247741	1.00[AMR][1000 genomes]
rs58003154	0.85[ASN][1000 genomes]
rs58263371	0.85[ASN][1000 genomes]
rs58502173	0.93[ASN][1000 genomes]
rs60410279	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs61115935	0.93[ASN][1000 genomes]
rs61223690	0.85[ASN][1000 genomes]
rs6885839	0.85[ASN][1000 genomes]
rs73779800	1.00[AMR][1000 genomes]
rs73779801	1.00[AMR][1000 genomes]
rs73782205	0.85[ASN][1000 genomes]
rs73782217	0.85[ASN][1000 genomes]
rs73782220	0.85[ASN][1000 genomes]
rs73782221	0.85[ASN][1000 genomes]
rs73782222	0.85[ASN][1000 genomes]
rs73782224	0.85[ASN][1000 genomes]
rs73782225	0.85[ASN][1000 genomes]
rs73782227	1.00[AMR][1000 genomes]
rs73782229	0.93[ASN][1000 genomes]
rs73782233	0.93[ASN][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	nsv830451	chr5:113684301-113829833	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr5:113728200-113732400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:113730200-113731800	Enhancers	H1 Cell Line	embryonic stem cell
3	chr5:113730800-113731600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr5:113730800-113731600	Enhancers	Pancreas	Pancrea
5	chr5:113731000-113732000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:113731200-113732200	Enhancers	Liver	Liver
7	chr5:113731400-113731800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:113731400-113731800	Enhancers	Brain Anterior Caudate	brain
9	chr5:113731400-113732000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr5:113731400-113732000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr5:113731400-113732000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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