Variant report

Variant	rs1577985
Chromosome Location	chr1:211334531-211334532
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11119680	0.94[AFR][1000 genomes]
rs11119690	0.81[EUR][1000 genomes]
rs11119698	0.95[AFR][1000 genomes]
rs1933523	0.85[AFR][1000 genomes]
rs3811395	0.94[AFR][1000 genomes]
rs4951729	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6540660	0.92[ASN][1000 genomes]
rs6663683	0.92[AFR][1000 genomes]
rs6703560	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211334200-211340400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:211334400-211336400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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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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