Variant report

Variant	rs7150534
Chromosome Location	chr14:39664767-39664768
allele	C/T
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:18)

rs_ID	r²[population]
rs17108984	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58306156	1.00[AMR][1000 genomes]
rs58506434	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59045671	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59143464	1.00[AMR][1000 genomes]
rs6571902	1.00[AMR][1000 genomes]
rs6571903	1.00[AMR][1000 genomes]
rs7146968	1.00[AMR][1000 genomes]
rs7154840	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73291602	1.00[AMR][1000 genomes]
rs73293324	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8006043	1.00[AMR][1000 genomes]
rs8010195	1.00[AMR][1000 genomes]
rs8010944	1.00[AMR][1000 genomes]
rs8011297	1.00[AMR][1000 genomes]
rs8013863	1.00[AMR][1000 genomes]
rs8015801	1.00[AMR][1000 genomes]
rs8018947	0.98[AFR][1000 genomes];1.00[AMR][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	nsv1246	chr14:39656597-39701520	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1053133	chr14:39657535-39770729	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv974270	chr14:39664152-39680061	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39654400-39672000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:39658000-39672400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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