Variant report

Variant	rs17881703
Chromosome Location	chr11:102398729-102398730
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11225310	1.00[ASN][1000 genomes]
rs12794864	1.00[ASN][1000 genomes]
rs17098329	1.00[ASN][1000 genomes]
rs17769668	1.00[ASN][1000 genomes]
rs33945990	1.00[ASN][1000 genomes]
rs34422940	1.00[ASN][1000 genomes]
rs58527547	1.00[ASN][1000 genomes]
rs59379441	1.00[ASN][1000 genomes]
rs59437179	1.00[ASN][1000 genomes]
rs60724341	1.00[ASN][1000 genomes]
rs61395048	1.00[ASN][1000 genomes]
rs61895369	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035567	chr11:102264516-102431607	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv469990	chr11:102335609-102413943	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv556150	chr11:102335609-102415859	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv468854	chr11:102336617-102413943	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv556151	chr11:102336617-102413943	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr11:102393400-102401200	Weak transcription	Pancreas	Pancrea
2	chr11:102393800-102399000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr11:102394000-102401200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr11:102397800-102399800	Enhancers	A549	lung
5	chr11:102398200-102399400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:102398200-102399600	Enhancers	Hela-S3	cervix
7	chr11:102398200-102400000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:102398200-102400000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr11:102398200-102400200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr11:102398400-102399000	Enhancers	HUVEC	blood vessel
11	chr11:102398400-102400000	Enhancers	HMEC	breast
12	chr11:102398400-102400200	Enhancers	NHEK	skin

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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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