Variant report

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEL1L-7	chr14:84373216-84373525	ENSG00000258532

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10148908	0.93[ASN][1000 genomes]
rs11159614	0.94[ASN][1000 genomes]
rs11159616	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11159623	0.91[AMR][1000 genomes]
rs11159624	0.91[AMR][1000 genomes]
rs12437313	0.88[AMR][1000 genomes]
rs12587946	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12587963	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12588549	0.88[AMR][1000 genomes]
rs12590059	0.88[AMR][1000 genomes]
rs1511315	0.91[AMR][1000 genomes]
rs1698247	0.93[ASN][1000 genomes]
rs1698250	0.94[ASN][1000 genomes]
rs1705652	0.93[ASN][1000 genomes]
rs1705660	0.94[ASN][1000 genomes]
rs4899844	0.98[ASN][1000 genomes]
rs4904146	0.88[AMR][1000 genomes]
rs4904148	0.88[AMR][1000 genomes]
rs6574761	1.00[YRI][hapmap]
rs7156908	1.00[YRI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902159	chr14:84336944-84447356	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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