Variant report

Variant	rs61602379
Chromosome Location	chr11:119935440-119935441
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10431043	0.91[ASN][1000 genomes]
rs10892514	0.81[ASN][1000 genomes]
rs10892519	0.87[ASN][1000 genomes]
rs10892521	0.86[ASN][1000 genomes]
rs11217636	0.81[ASN][1000 genomes]
rs11217637	0.81[ASN][1000 genomes]
rs11217647	0.86[ASN][1000 genomes]
rs11217665	0.92[ASN][1000 genomes]
rs11217666	0.92[ASN][1000 genomes]
rs12223988	0.81[ASN][1000 genomes]
rs12225953	0.92[ASN][1000 genomes]
rs12573999	0.87[ASN][1000 genomes]
rs12574203	0.83[ASN][1000 genomes]
rs12575245	0.84[ASN][1000 genomes]
rs56745971	0.81[ASN][1000 genomes]
rs56778655	0.82[ASN][1000 genomes]
rs57589469	0.87[ASN][1000 genomes]
rs58844530	0.91[ASN][1000 genomes]
rs59838357	0.95[ASN][1000 genomes]
rs60914924	1.00[ASN][1000 genomes]
rs60967975	0.82[ASN][1000 genomes]
rs61218458	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv832285	chr11:119789595-119957724	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv508657	chr11:119891578-119971212	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119922600-119936000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:119933600-119938000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:119933800-119936800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:119933800-119938400	Weak transcription	Fetal Kidney	kidney
5	chr11:119933800-119939000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:119934200-119939000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:119934800-119936200	Enhancers	Esophagus	oesophagus
8	chr11:119934800-119936600	Weak transcription	Brain Hippocampus Middle	brain
9	chr11:119934800-119936800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr11:119935000-119938000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:119935200-119943000	Weak transcription	Brain Angular Gyrus	brain
12	chr11:119935400-119936800	Weak transcription	Fetal Brain Female	brain
13	chr11:119935400-119937200	Weak transcription	Fetal Brain Male	brain

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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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