Variant report

Variant	rs7130424
Chromosome Location	chr11:92713693-92713694
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11020125	0.87[EUR][1000 genomes]
rs11020126	0.87[EUR][1000 genomes]
rs12272268	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12275765	0.96[EUR][1000 genomes]
rs12277904	1.00[EUR][1000 genomes]
rs12283180	0.96[EUR][1000 genomes]
rs12290860	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12292400	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs271042	0.96[EUR][1000 genomes]
rs55985911	1.00[EUR][1000 genomes]
rs61747139	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6483208	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6483209	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6483210	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7127128	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044571	chr11:92495213-92742314	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv555903	chr11:92640787-92877533	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv555904	chr11:92640787-92881933	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:92710600-92714000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:92711400-92713800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:92711400-92714000	Enhancers	HMEC	breast
4	chr11:92711800-92714000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:92712200-92717600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:92713200-92713800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:92713200-92714000	Bivalent Enhancer	Fetal Muscle Leg	muscle
8	chr11:92713200-92717200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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