Variant report

Variant	rs10077918
Chromosome Location	chr5:36590603-36590604
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10053299	1.00[EUR][1000 genomes]
rs10054009	1.00[EUR][1000 genomes]
rs10056349	1.00[EUR][1000 genomes]
rs10056352	1.00[EUR][1000 genomes]
rs10056466	1.00[EUR][1000 genomes]
rs10058111	1.00[EUR][1000 genomes]
rs10058115	1.00[EUR][1000 genomes]
rs10058314	1.00[EUR][1000 genomes]
rs10058422	1.00[EUR][1000 genomes]
rs10058564	1.00[EUR][1000 genomes]
rs10061999	1.00[EUR][1000 genomes]
rs10073164	1.00[EUR][1000 genomes]
rs10073279	1.00[EUR][1000 genomes]
rs10077206	1.00[EUR][1000 genomes]
rs10079668	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10085047	1.00[EUR][1000 genomes]
rs10085102	1.00[EUR][1000 genomes]
rs11954566	1.00[EUR][1000 genomes]
rs13354988	1.00[EUR][1000 genomes]
rs28376702	1.00[EUR][1000 genomes]
rs28479598	1.00[EUR][1000 genomes]
rs28505610	1.00[EUR][1000 genomes]
rs28523559	1.00[EUR][1000 genomes]
rs28647761	1.00[EUR][1000 genomes]
rs56288606	1.00[EUR][1000 genomes]
rs57336573	1.00[EUR][1000 genomes]
rs58556892	1.00[EUR][1000 genomes]
rs59457338	1.00[EUR][1000 genomes]
rs60856949	1.00[EUR][1000 genomes]
rs61246645	1.00[EUR][1000 genomes]
rs61448540	1.00[EUR][1000 genomes]
rs73089650	1.00[EUR][1000 genomes]
rs73089652	1.00[EUR][1000 genomes]
rs73089653	1.00[EUR][1000 genomes]
rs73089661	1.00[EUR][1000 genomes]
rs73089667	1.00[EUR][1000 genomes]
rs73089669	1.00[EUR][1000 genomes]
rs73089699	1.00[EUR][1000 genomes]
rs73089701	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	nsv492319	chr5:36570707-37061019	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv881025	chr5:36575021-36613053	Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
3	nsv830263	chr5:36576504-36755093	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36584800-36590800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr5:36585400-36590800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr5:36586200-36590800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr5:36587800-36591400	Weak transcription	Left Ventricle	heart
5	chr5:36589600-36591600	Weak transcription	Right Atrium	heart
6	chr5:36590400-36590800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr5:36590400-36591800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:36590600-36590800	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr5:36590600-36591200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr5:36590600-36591400	Enhancers	Brain Anterior Caudate	brain
11	chr5:36590600-36591800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr5:36590600-36591800	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr5:36590600-36591800	Enhancers	Brain Substantia Nigra	brain
14	chr5:36590600-36592000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:36590600-36592000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:36590600-36592000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr5:36590600-36592000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:36590600-36592200	Enhancers	HUES6 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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