Variant report

Variant	rs2813693
Chromosome Location	chr1:216868535-216868536
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10127480	0.83[JPT][hapmap]
rs1339341	0.83[YRI][hapmap]
rs2813705	0.92[AFR][1000 genomes]
rs3862956	1.00[CEU][hapmap];0.82[CHB][hapmap];0.93[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4085154	0.92[CEU][hapmap];0.90[CHB][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4846649	0.92[CEU][hapmap];0.85[CHB][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216856400-216869800	Weak transcription	Psoas Muscle	Psoas
2	chr1:216864000-216873200	Weak transcription	Fetal Heart	heart
3	chr1:216868200-216894000	Weak transcription	Placenta	Placenta

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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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