Variant report

Variant	rs4738654
Chromosome Location	chr8:59152769-59152770
allele	A/G
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:18)

rs_ID	r²[population]
rs10504251	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12546637	0.89[ASN][1000 genomes]
rs12546705	0.89[ASN][1000 genomes]
rs12677024	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12680043	0.93[ASN][1000 genomes]
rs13250098	0.89[ASN][1000 genomes]
rs13280150	0.89[ASN][1000 genomes]
rs16923211	0.92[CHB][hapmap]
rs34931209	0.89[ASN][1000 genomes]
rs4738653	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4738659	0.85[ASN][1000 genomes]
rs4738665	0.81[ASN][1000 genomes]
rs62512350	0.81[ASN][1000 genomes]
rs6995423	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6995739	0.89[ASN][1000 genomes]
rs6998045	0.89[ASN][1000 genomes]
rs9643501	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9643504	0.93[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59147400-59161000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:59150800-59155000	Weak transcription	Fetal Brain Female	brain
3	chr8:59151400-59154800	Weak transcription	Fetal Brain Male	brain

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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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