Variant report

Variant	rs195401
Chromosome Location	chr6:37318757-37318758
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1224294	1.00[AMR][1000 genomes]
rs149701	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs149717	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1756998	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs195387	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs195404	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs195411	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs195749	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2622894	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs262921	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs376155	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs415941	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6912213	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37315800-37321200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr6:37316000-37321200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:37317200-37321000	Weak transcription	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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