Variant report

Variant	rs1865370
Chromosome Location	chr18:44930510-44930511
allele	C/T
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:18)

rs_ID	r²[population]
rs10083906	0.98[ASN][1000 genomes]
rs10853551	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10853552	0.98[ASN][1000 genomes]
rs11082575	0.87[YRI][hapmap]
rs11082578	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11082579	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11082582	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11082583	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs11875780	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12955529	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12956050	0.98[ASN][1000 genomes]
rs34885067	0.98[ASN][1000 genomes]
rs4407146	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7230517	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7230554	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7231544	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7231597	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8088348	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][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	nsv833641	chr18:44815063-45020202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
2	esv1801141	chr18:44908270-44955409	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44930000-44931200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr18:44930000-44932800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr18:44930000-44932800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr18:44930400-44931800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr18:44930400-44931800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr18:44930400-44932000	Enhancers	H1 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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