Variant report

Variant	rs59184670
Chromosome Location	chr14:97490885-97490886
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10134981	0.89[AMR][1000 genomes]
rs10148082	0.89[AMR][1000 genomes]
rs17094877	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17094884	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17094887	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2024663	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56871417	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58955411	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs710271	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7149193	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs742881	0.98[EUR][1000 genomes];0.95[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	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948620	chr14:97334444-98133191	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv832867	chr14:97365919-97541763	Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1048462	chr14:97421360-97804598	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97489200-97491800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr14:97489200-97494600	Enhancers	H1 Cell Line	embryonic stem cell
3	chr14:97489400-97491800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr14:97489400-97494000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr14:97489600-97491800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr14:97489600-97491800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr14:97489600-97495200	Enhancers	H9 Cell Line	embryonic stem cell
8	chr14:97489800-97491000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr14:97489800-97491800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr14:97489800-97491800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr14:97490000-97495200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:97490200-97491800	Enhancers	Brain Germinal Matrix	brain
13	chr14:97490400-97491800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr14:97490600-97495200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr14:97490800-97491000	Bivalent Enhancer	Fetal Brain Male	brain
16	chr14:97490800-97491800	Enhancers	Fetal Brain Female	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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