Variant report

Variant	rs215505
Chromosome Location	chr14:79302929-79302930
allele	A/T
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]
rs154310	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17108301	1.00[ASN][1000 genomes]
rs17108303	1.00[ASN][1000 genomes]
rs17108324	0.83[ASN][1000 genomes]
rs31355	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs31357	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs31361	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs31363	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs42568	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs749919	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79302000-79303000	Enhancers	Fetal Brain Female	brain
2	chr14:79302400-79303600	Enhancers	Brain Angular Gyrus	brain
3	chr14:79302600-79303200	Weak transcription	Brain Germinal Matrix	brain
4	chr14:79302800-79303800	Weak transcription	Fetal Brain Male	brain

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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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