Variant report

Variant	rs9962024
Chromosome Location	chr18:25228960-25228961
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11083220	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12458483	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1362726	0.85[EUR][1000 genomes]
rs1420936	0.85[EUR][1000 genomes]
rs1420938	0.85[EUR][1000 genomes]
rs1420943	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1420964	0.83[EUR][1000 genomes]
rs1420965	0.85[EUR][1000 genomes]
rs1477186	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17721591	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2041978	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7232506	0.83[EUR][1000 genomes]
rs8083881	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8088804	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8091588	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8092380	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs888291	0.84[EUR][1000 genomes]
rs888295	0.82[EUR][1000 genomes]
rs9304509	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs971244	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9952141	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9952238	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9958477	0.87[EUR][1000 genomes]
rs9963988	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9965477	0.87[AMR][1000 genomes];0.90[EUR][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	esv2761996	chr18:24866083-25818618	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv1061993	chr18:25211720-25239455	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1067348	chr18:25213808-25239455	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv833604	chr18:25226727-25417423	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:25228400-25229600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr18:25228600-25230200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr18:25228600-25230200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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