Variant report

Variant	rs10898821
Chromosome Location	chr11:71831312-71831313
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs588693	1.00[YRI][hapmap];1.00[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	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71824800-71834600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:71827400-71833400	Weak transcription	Hela-S3	cervix
3	chr11:71828000-71834200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:71828200-71834200	Weak transcription	NHEK	skin
5	chr11:71828400-71850800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:71829400-71831400	Enhancers	Primary B cells from cord blood	blood
7	chr11:71829400-71831400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr11:71830000-71832200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr11:71830400-71832000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:71830400-71833400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr11:71830600-71833200	Weak transcription	K562	blood
12	chr11:71830800-71832200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr11:71831200-71835000	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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