Variant report

Variant	rs7214520
Chromosome Location	chr17:15072451-15072452
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10521298	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4792577	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4792578	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4792579	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4792581	0.87[EUR][1000 genomes]
rs62072220	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072244	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072246	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62072247	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7215556	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7538	1.00[CHB][hapmap]
rs8078320	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9891766	0.85[EUR][1000 genomes]
rs9892470	0.85[EUR][1000 genomes]
rs9894434	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9899726	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9914844	0.85[EUR][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	nsv1066329	chr17:14983674-15294071	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv543212	chr17:14983674-15294071	Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
3	nsv1990	chr17:15041267-15094044	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv492304	chr17:15043353-15611753	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15071800-15072600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr17:15071800-15073400	Enhancers	Fetal Stomach	stomach
3	chr17:15072000-15072600	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr17:15072000-15072600	Bivalent Enhancer	Fetal Lung	lung
5	chr17:15072000-15072600	Enhancers	Right Atrium	heart
6	chr17:15072200-15072600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr17:15072200-15072600	Enhancers	Placenta	Placenta
8	chr17:15072400-15072600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr17:15072400-15072600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr17:15072400-15074400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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