Variant report

Variant	rs17102614
Chromosome Location	chr14:65806115-65806116
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12100674	1.00[EUR][1000 genomes]
rs17102582	1.00[EUR][1000 genomes]
rs17102621	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17102690	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17102756	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2069276	0.83[AFR][1000 genomes]
rs28465145	1.00[EUR][1000 genomes]
rs56966413	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59324651	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60514832	1.00[EUR][1000 genomes]
rs61004469	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7154681	1.00[EUR][1000 genomes]
rs8010623	1.00[EUR][1000 genomes]
rs8012057	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8014977	1.00[EUR][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	nsv832817	chr14:65637069-65810406	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
2	nsv832818	chr14:65706859-65882320	Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1036403	chr14:65724229-66208114	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
4	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
5	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 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	chr14:65796000-65807200	Enhancers	Placenta	Placenta
2	chr14:65803400-65806600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr14:65803400-65806600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr14:65803400-65806800	Weak transcription	Gastric	stomach
5	chr14:65803400-65811600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr14:65803400-65813200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr14:65803400-65813200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr14:65803400-65813400	Weak transcription	NHLF	lung
9	chr14:65803400-65821000	Weak transcription	Esophagus	oesophagus
10	chr14:65803600-65806800	Weak transcription	NHDF-Ad	bronchial
11	chr14:65805400-65806400	Weak transcription	Fetal Intestine Large	intestine
12	chr14:65805400-65806400	Weak transcription	Stomach Mucosa	stomach
13	chr14:65805400-65806600	Weak transcription	Fetal Intestine Small	intestine
14	chr14:65805800-65806200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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