Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:72694736..72697580-chr14:72698002..72700652,3	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10131012	0.82[ASN][1000 genomes]
rs10134489	0.81[ASN][1000 genomes]
rs10134542	0.82[ASN][1000 genomes]
rs10143449	0.81[ASN][1000 genomes]
rs10149098	0.82[ASN][1000 genomes]
rs10150159	0.82[ASN][1000 genomes]
rs10150242	0.81[ASN][1000 genomes]
rs12148024	0.86[ASN][1000 genomes]
rs12432346	0.94[ASN][1000 genomes]
rs12432632	0.90[ASN][1000 genomes]
rs12894979	0.88[ASN][1000 genomes]
rs1402056	0.89[ASN][1000 genomes]
rs1402061	0.80[EUR][1000 genomes]
rs1520326	0.86[ASN][1000 genomes]
rs1544487	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1558071	0.82[ASN][1000 genomes]
rs1558073	0.81[ASN][1000 genomes]
rs17180251	0.82[ASN][1000 genomes]
rs2079502	0.85[ASN][1000 genomes]
rs2108466	0.85[ASN][1000 genomes]
rs2238212	0.81[ASN][1000 genomes]
rs2238213	0.82[ASN][1000 genomes]
rs2238217	0.81[ASN][1000 genomes]
rs2238218	0.82[ASN][1000 genomes]
rs2239257	0.81[ASN][1000 genomes]
rs2239261	0.82[ASN][1000 genomes]
rs2283407	0.81[EUR][1000 genomes]
rs2332807	0.92[ASN][1000 genomes]
rs2332808	0.82[ASN][1000 genomes]
rs3784049	0.86[ASN][1000 genomes]
rs4903004	0.82[ASN][1000 genomes]
rs6574055	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6574056	0.94[ASN][1000 genomes]
rs6574057	0.81[ASN][1000 genomes]
rs699369	0.84[ASN][1000 genomes]
rs7157673	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7350728	0.82[ASN][1000 genomes]
rs740337	0.82[ASN][1000 genomes]
rs8007922	0.82[ASN][1000 genomes]
rs847241	0.82[ASN][1000 genomes]
rs847305	0.81[AMR][1000 genomes]
rs847345	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1041492	chr14:72634606-72768970	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv977614	chr14:72696106-72702781	Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72687800-72700200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr14:72687800-72705800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:72699400-72699800	Enhancers	Right Ventricle	heart
4	chr14:72699600-72700600	Enhancers	Left Ventricle	heart

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