Variant report

Variant	rs61939865
Chromosome Location	chr12:118273523-118273524
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10850906	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12318877	0.97[EUR][1000 genomes]
rs17439762	1.00[ASN][1000 genomes]
rs7309589	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7358657	0.89[EUR][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118267600-118274600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr12:118267800-118274800	Weak transcription	Brain Anterior Caudate	brain
3	chr12:118267800-118274800	Weak transcription	Pancreas	Pancrea
4	chr12:118269600-118274400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr12:118270600-118274800	Weak transcription	Dnd41	blood
6	chr12:118271200-118274400	Weak transcription	A549	lung
7	chr12:118271400-118274800	Weak transcription	HSMM	muscle
8	chr12:118271600-118274400	Weak transcription	NHDF-Ad	bronchial
9	chr12:118271600-118275000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr12:118272000-118274000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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