Variant report

Variant	rs73620033
Chromosome Location	chr6:130804958-130804959
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs73621742	1.00[AFR][1000 genomes]
rs73621755	1.00[AFR][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	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:130802800-130806600	Enhancers	Dnd41	blood
2	chr6:130803200-130805400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr6:130803200-130805800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr6:130803200-130805800	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr6:130803400-130805000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:130803400-130805200	Enhancers	Primary T cells from cord blood	blood
7	chr6:130803400-130805600	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr6:130804400-130805800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr6:130804600-130805600	Weak transcription	Ovary	ovary
10	chr6:130804600-130806000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:130804800-130805800	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr6:130804800-130806200	Weak transcription	Osteobl	bone

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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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