Variant report

Variant	rs4768302
Chromosome Location	chr12:41038005-41038006
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs55827941	0.96[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs56268203	0.96[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs57762151	0.96[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs58269853	0.92[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs59015015	0.82[AFR][1000 genomes]
rs60776914	0.96[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs73108912	0.88[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs73123168	0.96[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs73123171	0.94[AFR][1000 genomes];0.84[EUR][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	nsv899033	chr12:40758652-41122288	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv832378	chr12:40943111-41132305	Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr12:41037000-41041800	Enhancers	Fetal Lung	lung
2	chr12:41037200-41040800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr12:41037800-41038400	Weak transcription	Fetal Kidney	kidney

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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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