Variant report

Variant	rs11048420
Chromosome Location	chr12:26314380-26314381
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1077584	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11048419	0.87[AFR][1000 genomes]
rs12300500	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1471506	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4963968	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56686254	0.96[AFR][1000 genomes]
rs7134610	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7304527	0.82[AFR][1000 genomes]
rs7309947	0.94[AFR][1000 genomes]
rs7316143	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7979429	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26308000-26316800	Weak transcription	HMEC	breast
2	chr12:26310200-26316600	Enhancers	Primary B cells from peripheral blood	blood
3	chr12:26312200-26315600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:26312400-26317200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr12:26313600-26314800	Weak transcription	GM12878-XiMat	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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