Variant report

Variant	rs7146147
Chromosome Location	chr14:85036660-85036661
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10151029	1.00[EUR][1000 genomes]
rs1449096	0.85[ASN][1000 genomes]
rs1551011	0.85[ASN][1000 genomes]
rs2372778	0.85[ASN][1000 genomes]
rs2922628	1.00[EUR][1000 genomes]
rs2998296	0.85[ASN][1000 genomes]
rs2998297	1.00[EUR][1000 genomes]
rs55798405	1.00[EUR][1000 genomes]
rs58840513	1.00[EUR][1000 genomes]
rs60743202	1.00[ASN][1000 genomes]
rs72687280	1.00[EUR][1000 genomes]
rs72687282	1.00[EUR][1000 genomes]
rs72687290	1.00[EUR][1000 genomes]
rs72687292	1.00[EUR][1000 genomes]
rs72687293	1.00[EUR][1000 genomes]
rs72687296	1.00[EUR][1000 genomes]
rs72687298	1.00[EUR][1000 genomes]
rs72687300	1.00[EUR][1000 genomes]
rs72687302	1.00[EUR][1000 genomes]
rs72688804	1.00[EUR][1000 genomes]
rs72688806	1.00[EUR][1000 genomes]
rs72688808	1.00[EUR][1000 genomes]
rs72688814	1.00[EUR][1000 genomes]
rs72688883	1.00[EUR][1000 genomes]
rs72688893	1.00[EUR][1000 genomes]
rs72688898	1.00[EUR][1000 genomes]
rs72690604	1.00[EUR][1000 genomes]
rs72690616	1.00[EUR][1000 genomes]
rs72690617	1.00[EUR][1000 genomes]
rs72690619	1.00[EUR][1000 genomes]
rs72690622	1.00[EUR][1000 genomes]
rs72690624	1.00[EUR][1000 genomes]
rs72706914	1.00[EUR][1000 genomes]
rs72706915	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	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046875	chr14:84993510-85193250	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1052415	chr14:85001891-85078853	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85036200-85036800	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr14:85036200-85037000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr14:85036400-85037000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr14:85036600-85046200	Weak transcription	iPS-18 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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