Variant report

Variant	rs73727538
Chromosome Location	chr6:24378865-24378866
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs57322986	1.00[EUR][1000 genomes]
rs58118499	1.00[EUR][1000 genomes]
rs73391991	1.00[EUR][1000 genomes]
rs73394039	1.00[EUR][1000 genomes]
rs73394050	1.00[EUR][1000 genomes]
rs73725407	1.00[EUR][1000 genomes]
rs73725408	1.00[EUR][1000 genomes]
rs73727536	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73727537	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73727539	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73727541	1.00[EUR][1000 genomes]
rs73727546	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	nsv1026638	chr6:24347972-24475300	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24372800-24381600	Weak transcription	Fetal Intestine Small	intestine
2	chr6:24376800-24383200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:24377200-24379400	Genic enhancers	HepG2	liver
4	chr6:24378400-24379200	Enhancers	GM12878-XiMat	blood
5	chr6:24378800-24379000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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