Variant report

Variant	rs4907951
Chromosome Location	chr1:102166616-102166617
allele	A/C
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:12)

rs_ID	r²[population]
rs11164273	0.84[EUR][1000 genomes]
rs11164274	0.87[AFR][1000 genomes]
rs12096354	0.80[AFR][1000 genomes]
rs1601235	0.84[EUR][1000 genomes]
rs1843112	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4907950	0.87[EUR][1000 genomes]
rs55785127	0.80[AFR][1000 genomes]
rs56064810	0.87[EUR][1000 genomes]
rs56173817	0.84[ASN][1000 genomes]
rs56221742	0.84[EUR][1000 genomes]
rs7529743	0.82[AMR][1000 genomes]
rs7537078	0.87[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv870459	chr1:102112168-102166616	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:102166200-102166800	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr1:102166400-102167800	Enhancers	Dnd41	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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