Variant report

Variant	rs1779209
Chromosome Location	chr10:18514561-18514562
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11013065	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1277745	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1277746	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1277748	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1277749	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1277750	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1277754	0.97[ASN][1000 genomes]
rs1757225	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1757226	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1779207	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1779217	0.85[ASN][1000 genomes]
rs2250996	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2482110	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18511200-18520400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr10:18511400-18516200	Weak transcription	Fetal Heart	heart
3	chr10:18512400-18518400	Weak transcription	NHLF	lung
4	chr10:18513000-18514600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr10:18513600-18515400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:18513600-18515400	Enhancers	Ovary	ovary
7	chr10:18514000-18514600	Weak transcription	Fetal Stomach	stomach
8	chr10:18514000-18518800	Weak transcription	Colon Smooth Muscle	Colon
9	chr10:18514000-18522400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr10:18514000-18522800	Weak transcription	Esophagus	oesophagus
11	chr10:18514400-18518200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:18514400-18524400	Weak transcription	Stomach Smooth Muscle	stomach
13	chr10:18514400-18525600	Weak transcription	Fetal Lung	lung
14	chr10:18514400-18526600	Weak transcription	Rectal Smooth Muscle	rectum

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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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