Variant report

Variant	rs9992040
Chromosome Location	chr4:18737754-18737755
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs1356473	0.81[AFR][1000 genomes]
rs28398433	0.81[AFR][1000 genomes]
rs28402993	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28439715	1.00[AMR][1000 genomes]
rs28671154	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003931	chr4:18241575-18849898	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv533087	chr4:18362040-19176896	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv532708	chr4:18596861-19176896	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv878722	chr4:18668957-18741988	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv878723	chr4:18668957-19005988	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:18735200-18737800	Enhancers	Fetal Heart	heart
2	chr4:18735200-18737800	Enhancers	Rectal Smooth Muscle	rectum
3	chr4:18735800-18737800	Enhancers	Colon Smooth Muscle	Colon
4	chr4:18736400-18737800	Enhancers	Fetal Lung	lung
5	chr4:18736600-18739200	Weak transcription	Brain Anterior Caudate	brain
6	chr4:18736600-18739200	Weak transcription	Brain Substantia Nigra	brain
7	chr4:18736600-18739600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr4:18736800-18739200	Weak transcription	Brain Hippocampus Middle	brain
9	chr4:18737000-18739200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr4:18737600-18739200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

Quick Search:

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

what's new

Quick links