Variant report

Variant	rs11188776
Chromosome Location	chr10:98229546-98229547
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10882797	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs10882806	1.00[EUR][1000 genomes]
rs11188787	0.95[ASN][1000 genomes]
rs11188794	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11188806	1.00[EUR][1000 genomes]
rs11188824	1.00[EUR][1000 genomes]
rs12218172	0.95[ASN][1000 genomes]
rs9633705	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3413353	chr10:98039370-98561524	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv831950	chr10:98080972-98245434	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98228200-98230400	Enhancers	Dnd41	blood
2	chr10:98228400-98229800	Enhancers	Fetal Thymus	thymus
3	chr10:98228800-98230000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:98229000-98229600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr10:98229000-98229600	Weak transcription	Brain Hippocampus Middle	brain
6	chr10:98229000-98230000	Enhancers	Fetal Brain Male	brain
7	chr10:98229200-98229600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr10:98229200-98229600	Enhancers	Fetal Brain Female	brain
9	chr10:98229200-98230000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr10:98229200-98230200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr10:98229200-98230400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr10:98229400-98229600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr10:98229400-98231400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr10:98229400-98239400	Weak transcription	Right Ventricle	heart

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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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