Variant report

Variant	rs6034565
Chromosome Location	chr20:16645278-16645279
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11697065	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11699089	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55719178	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6135843	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73105293	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73105295	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73109533	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73109535	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73109536	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73109538	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73109541	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:16641600-16646800	Enhancers	Fetal Muscle Trunk	muscle
2	chr20:16641800-16645800	Enhancers	Fetal Muscle Leg	muscle
3	chr20:16642600-16645600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr20:16644200-16645400	Enhancers	HSMMtube	muscle

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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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