Variant report

Variant	rs10949008
Chromosome Location	chr6:13879481-13879482
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12207817	0.90[EUR][1000 genomes]
rs12529958	0.89[EUR][1000 genomes]
rs13201631	0.92[EUR][1000 genomes]
rs2209250	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35139352	0.90[EUR][1000 genomes]
rs4712134	0.92[EUR][1000 genomes]
rs62385894	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6919722	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9475717	0.89[EUR][1000 genomes]
rs9475727	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13874800-13881800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:13875000-13880400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr6:13878600-13880400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:13879400-13879600	Weak transcription	Esophagus	oesophagus

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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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