Variant report

Variant	rs632549
Chromosome Location	chr11:105836923-105836924
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1271104	1.00[YRI][hapmap]
rs2847179	1.00[AFR][1000 genomes]
rs473281	1.00[AFR][1000 genomes]
rs481203	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs503938	1.00[YRI][hapmap]
rs515931	1.00[YRI][hapmap]
rs517287	1.00[AFR][1000 genomes]
rs534788	1.00[YRI][hapmap]
rs539216	1.00[AFR][1000 genomes]
rs551893	1.00[YRI][hapmap]
rs558324	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs559190	0.86[AFR][1000 genomes]
rs584783	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs590908	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs592759	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs605666	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs611278	1.00[AFR][1000 genomes]
rs628230	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs630885	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs636686	0.86[AFR][1000 genomes]
rs638554	1.00[AFR][1000 genomes]
rs640354	0.86[AFR][1000 genomes]
rs648155	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs656636	0.86[AFR][1000 genomes]
rs659654	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs668564	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs669658	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs680049	1.00[AFR][1000 genomes]
rs688863	1.00[YRI][hapmap]
rs694854	1.00[AFR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105827400-105850200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:105831600-105838600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr11:105836200-105837000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr11:105836400-105837000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr11:105836400-105837000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr11:105836400-105837200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr11:105836400-105837200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr11:105836600-105837200	Enhancers	Brain Substantia Nigra	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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