Variant report

Variant	rs72906278
Chromosome Location	chr11:46171222-46171223
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11038785	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12361705	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34642764	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46170400-46171800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:46170600-46171400	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr11:46170800-46172000	Enhancers	K562	blood
4	chr11:46171000-46171600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr11:46171000-46171600	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr11:46171200-46172800	Weak transcription	iPS DF 6.9 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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