Variant report

Variant	rs2051153
Chromosome Location	chr1:61537695-61537696
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11207690	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11207691	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11207692	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11207694	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12130085	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12404093	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12406426	0.87[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61535400-61541200	Weak transcription	HepG2	liver
2	chr1:61537200-61537800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:61537600-61537800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:61537600-61540600	Weak transcription	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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