Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:37667647..37669347-chr2:37672463..37673987,2	K562	blood:

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

rs_ID	r²[population]
rs13425396	0.92[EUR][1000 genomes]
rs17020676	0.89[EUR][1000 genomes]
rs17020693	0.89[EUR][1000 genomes]
rs17020696	0.89[EUR][1000 genomes]
rs57223658	0.89[EUR][1000 genomes]
rs60003859	0.89[EUR][1000 genomes]
rs61022900	0.86[EUR][1000 genomes]
rs61356018	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6708554	0.86[EUR][1000 genomes]
rs6708931	0.86[EUR][1000 genomes]
rs6711805	0.89[EUR][1000 genomes]
rs6727245	0.89[EUR][1000 genomes]
rs6739990	0.89[EUR][1000 genomes]
rs6741256	0.86[EUR][1000 genomes]
rs6751874	0.89[EUR][1000 genomes]
rs6752214	0.89[EUR][1000 genomes]
rs6752559	0.86[EUR][1000 genomes]
rs6755472	0.89[EUR][1000 genomes]
rs6755835	0.89[EUR][1000 genomes]
rs6756253	0.89[EUR][1000 genomes]
rs72879949	0.86[EUR][1000 genomes]
rs72879952	0.89[EUR][1000 genomes]
rs72879959	0.89[EUR][1000 genomes]
rs72879966	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72879969	0.89[EUR][1000 genomes]
rs72879979	0.89[EUR][1000 genomes]
rs72879983	0.89[EUR][1000 genomes]
rs72881514	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72881515	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72881519	0.92[EUR][1000 genomes]
rs72881552	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72881557	1.00[EUR][1000 genomes]
rs72881560	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7603115	0.80[EUR][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	nsv833814	chr2:37643132-37840247	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv456374	chr2:37669487-37868214	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv470453	chr2:37669487-37868214	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv581473	chr2:37669487-37868214	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37669200-37675200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:37670000-37678400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:37672800-37676600	Weak transcription	Aorta	Aorta

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