Variant report

Variant	rs1819256
Chromosome Location	chr1:92861155-92861156
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11164423	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs12070923	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs12078746	0.88[AFR][1000 genomes]
rs12090761	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs12098095	0.87[AFR][1000 genomes]
rs17131621	0.82[AFR][1000 genomes]
rs55993081	0.87[AFR][1000 genomes]
rs56665661	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs57992264	0.90[AFR][1000 genomes]
rs6603970	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6662381	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs6662565	0.87[AFR][1000 genomes]
rs6681027	0.90[AFR][1000 genomes]
rs72960872	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs7535181	0.90[AFR][1000 genomes]
rs7546528	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92853800-92862000	Weak transcription	HSMM	muscle
2	chr1:92854400-92862800	Weak transcription	Thymus	Thymus
3	chr1:92854600-92862000	Weak transcription	Pancreas	Pancrea
4	chr1:92854600-92863400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr1:92854800-92864600	Weak transcription	Spleen	Spleen

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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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