Variant report

Variant	rs10022576
Chromosome Location	chr4:30332185-30332186
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10010447	0.84[ASN][1000 genomes]
rs10020607	0.80[ASN][1000 genomes]
rs10030599	0.80[ASN][1000 genomes]
rs10050144	0.84[ASN][1000 genomes]
rs16883183	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16883243	0.84[ASN][1000 genomes]
rs16883246	0.91[ASN][1000 genomes]
rs2164180	0.84[ASN][1000 genomes]
rs28367258	0.84[ASN][1000 genomes]
rs28608614	0.84[ASN][1000 genomes]
rs28754328	0.84[ASN][1000 genomes]
rs28889636	0.84[ASN][1000 genomes]
rs6846199	0.84[ASN][1000 genomes]
rs7675877	0.84[ASN][1000 genomes]
rs7676526	0.84[ASN][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	nsv878804	chr4:30162762-30412195	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30327800-30332600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:30332000-30332600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:30332000-30332600	Weak transcription	H1 Derived Neuronal Progenitor 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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