Variant report

Variant	rs849304
Chromosome Location	chr7:106656413-106656414
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10234225	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12113322	0.87[EUR][1000 genomes]
rs17153745	0.93[EUR][1000 genomes]
rs6954575	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7795821	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7798500	0.86[EUR][1000 genomes]
rs7807247	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:106655400-106656800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:106655400-106657400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr7:106655600-106658400	Weak transcription	Adipose Nuclei	Adipose
4	chr7:106655600-106659400	Enhancers	K562	blood

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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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