Variant report

Variant	rs12283645
Chromosome Location	chr11:102442839-102442840
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11225340	1.00[AMR][1000 genomes]
rs11225341	1.00[AMR][1000 genomes]
rs11225342	1.00[AMR][1000 genomes]
rs11225379	0.83[AFR][1000 genomes]
rs11825664	1.00[AMR][1000 genomes]
rs12289419	1.00[AMR][1000 genomes]
rs17098686	1.00[AMR][1000 genomes]
rs7125086	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	esv1815657	chr11:102413582-102490794	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102434600-102446600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr11:102437200-102445000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:102442600-102444200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:102442800-102443000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:102442800-102447400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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