Variant report

Variant	rs1922120
Chromosome Location	chr10:23202847-23202848
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10828372	0.89[AFR][1000 genomes]
rs10828373	0.89[AFR][1000 genomes]
rs72818809	1.00[ASN][1000 genomes]
rs74121670	1.00[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	esv2764013	chr10:23087298-23239345	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23201000-23204000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr10:23201600-23203000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr10:23201600-23203400	Weak transcription	Ovary	ovary
4	chr10:23202200-23204000	Weak transcription	Fetal Kidney	kidney

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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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