Variant report

Variant	rs10025747
Chromosome Location	chr4:111207807-111207808
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]
rs12233726	0.92[EUR][1000 genomes]
rs12711004	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17440767	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17620645	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2713949	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4698825	0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4698826	0.94[EUR][1000 genomes]
rs4698827	0.94[EUR][1000 genomes]
rs4698828	0.94[EUR][1000 genomes]
rs4698829	0.94[EUR][1000 genomes]
rs4698830	0.94[EUR][1000 genomes]
rs72886465	0.92[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	nsv869392	chr4:110945459-111235071	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:111206800-111208000	Weak transcription	GM12878-XiMat	blood
2	chr4:111206800-111208600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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