Variant report

Variant	rs17096288
Chromosome Location	chr1:75591486-75591487
allele	C/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:11)

rs_ID	r²[population]
rs10493562	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs17096153	1.00[AFR][1000 genomes]
rs17096252	1.00[AFR][1000 genomes]
rs17096261	1.00[AFR][1000 genomes]
rs17096265	0.83[AFR][1000 genomes]
rs17096275	1.00[AFR][1000 genomes]
rs17096521	0.91[AFR][1000 genomes]
rs17096698	0.91[AFR][1000 genomes]
rs17096706	0.91[AFR][1000 genomes]
rs6678156	0.91[AFR][1000 genomes]
rs6685905	0.91[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv871743	chr1:75235082-75714554	Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3368999	chr1:75524762-75933220	Bivalent/Poised TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75590600-75591600	Bivalent Enhancer	Fetal Brain Male	brain
2	chr1:75590600-75591600	Bivalent/Poised TSS	Fetal Brain Female	brain
3	chr1:75591400-75592600	Weak transcription	Pancreas	Pancrea

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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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