Variant report

Variant	rs12359791
Chromosome Location	chr10:91330137-91330138
allele	C/T
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]
rs11185761	0.83[ASN][1000 genomes]
rs61855207	0.82[ASN][1000 genomes]
rs7392559	0.81[ASN][1000 genomes]
rs7908686	0.85[AMR][1000 genomes];0.86[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	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91324800-91332800	Weak transcription	Ovary	ovary
2	chr10:91325000-91333200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr10:91328000-91330200	Weak transcription	NHDF-Ad	bronchial
4	chr10:91328000-91334000	Weak transcription	Fetal Lung	lung
5	chr10:91328000-91334200	Weak transcription	NHLF	lung
6	chr10:91328200-91347200	Weak transcription	HSMM	muscle
7	chr10:91330000-91330400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte 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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