Variant report

Variant	rs12111126
Chromosome Location	chr6:117928566-117928567
allele	C/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]
rs28522156	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28628829	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9688553	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9689787	0.93[AFR][1000 genomes];1.00[AMR][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	nsv532050	chr6:117528154-118203005	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 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	chr6:117924600-117933200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr6:117924800-117928800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:117925000-117934600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:117926800-117929200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:117928200-117929600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr6:117928400-117928800	Enhancers	GM12878-XiMat	blood
7	chr6:117928400-117928800	Enhancers	Monocytes-CD14+_RO01746	blood

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Input of quick search could be:

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

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