Variant report

Variant	rs36002894
Chromosome Location	chr1:61525565-61525566
allele	A/T
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]
rs11207690	0.81[EUR][1000 genomes]
rs11207691	0.81[EUR][1000 genomes]
rs12402443	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12402756	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12404336	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12406426	0.97[EUR][1000 genomes]
rs12565220	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:61523600-61528000	Weak transcription	Brain Substantia Nigra	brain
2	chr1:61524400-61528000	Weak transcription	Liver	Liver
3	chr1:61524600-61528000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr1:61524800-61528200	Weak transcription	Cortex derived primary cultured neurospheres	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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