Variant report

Variant	rs4147204
Chromosome Location	chr1:176350944-176350945
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10913160	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1503124	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs184764	0.83[GIH][hapmap]
rs2175177	0.80[MEX][hapmap]
rs2221333	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2455724	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2455725	0.81[ASN][1000 genomes]
rs2455748	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2504473	0.83[GIH][hapmap]
rs2504479	0.81[ASN][1000 genomes]
rs2504480	0.81[ASN][1000 genomes]
rs2504492	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2504494	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2504499	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3123622	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4130088	0.81[ASN][1000 genomes]
rs4526571	0.82[CHD][hapmap];0.87[MEX][hapmap];0.84[TSI][hapmap]
rs4642850	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4650941	0.81[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:176348800-176353200	Enhancers	Fetal Intestine Large	intestine
2	chr1:176349600-176351000	Weak transcription	Fetal Intestine Small	intestine
3	chr1:176350600-176353600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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