Variant report

Variant	rs62269514
Chromosome Location	chr3:88628087-88628088
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17487324	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62269512	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62269513	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62269516	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62269530	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62269535	0.80[EUR][1000 genomes]
rs62269536	0.80[EUR][1000 genomes]
rs62271215	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62271216	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62271217	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6803194	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916330	chr3:88083580-88884125	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv3906	chr3:88609226-88654550	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1014703	chr3:88623532-88733631	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3394276	chr3:88626087-88628635	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
5	esv3431022	chr3:88626337-88628535	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
6	esv3323108	chr3:88626662-88628160	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:88627800-88628200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:88627800-88628200	Enhancers	H9 Derived Neuron 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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