Variant report

Variant	rs1881754
Chromosome Location	chr4:160293543-160293544
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10011640	1.00[EUR][1000 genomes]
rs11100220	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11930767	1.00[MEX][hapmap]
rs11946018	1.00[EUR][1000 genomes]
rs1317334	1.00[EUR][1000 genomes]
rs17038050	1.00[MEX][hapmap]
rs17038266	1.00[EUR][1000 genomes]
rs28463255	1.00[EUR][1000 genomes]
rs28628113	1.00[EUR][1000 genomes]
rs28728335	1.00[EUR][1000 genomes]
rs28757609	1.00[EUR][1000 genomes]
rs3897680	1.00[EUR][1000 genomes]
rs6818489	1.00[EUR][1000 genomes]
rs72971811	1.00[EUR][1000 genomes]
rs72971815	1.00[EUR][1000 genomes]
rs7659664	1.00[EUR][1000 genomes]
rs7660063	1.00[EUR][1000 genomes]
rs7660599	1.00[EUR][1000 genomes]
rs7679524	1.00[EUR][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	nsv1022771	chr4:160188801-160324683	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160275200-160303800	Weak transcription	Right Atrium	heart
2	chr4:160280200-160295200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:160289000-160295800	Weak transcription	Fetal Heart	heart
4	chr4:160291000-160299000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:160291200-160299800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:160293400-160293600	Enhancers	Spleen	Spleen
7	chr4:160293400-160293600	Enhancers	HSMMtube	muscle

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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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