Variant report

Variant	rs72939918
Chromosome Location	chr4:143846802-143846803
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11931930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11936161	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11938074	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11942298	1.00[AMR][1000 genomes]
rs11945219	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11945221	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11946952	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17016916	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17016965	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17016976	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60837660	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6814142	0.97[AFR][1000 genomes]
rs72937983	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72939905	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72939914	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72939930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7435181	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7657815	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7674856	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7694316	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880174	chr4:143639498-143848024	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv880175	chr4:143779613-143892252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv10580	chr4:143794158-143856359	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv830102	chr4:143820268-143953611	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143837400-143848800	Weak transcription	Aorta	Aorta
2	chr4:143844600-143847000	Enhancers	Rectal Smooth Muscle	rectum
3	chr4:143845400-143849600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:143845600-143848200	Weak transcription	Fetal Stomach	stomach
5	chr4:143845600-143848200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr4:143845600-143850400	Weak transcription	Fetal Intestine Large	intestine
7	chr4:143845600-143850400	Weak transcription	Fetal Intestine Small	intestine
8	chr4:143846800-143848000	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:143846800-143850600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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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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