Variant report

Variant	rs4766973
Chromosome Location	chr12:121064024-121064025
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11065176	0.87[ASN][1000 genomes]
rs12310124	0.87[ASN][1000 genomes]
rs12317166	0.86[ASN][1000 genomes]
rs12370780	0.87[ASN][1000 genomes]
rs4382980	0.81[ASN][1000 genomes]
rs4766974	0.88[ASN][1000 genomes]
rs7974387	0.87[ASN][1000 genomes]
rs7976299	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	nsv521928	chr12:121041728-121761800	Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 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	chr12:121063800-121066400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr12:121064000-121066600	Weak transcription	A549	lung
3	chr12:121064000-121069000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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