Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:127765926..127767639-chr4:127769595..127772371,2	K562	blood:

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10446736	0.90[ASN][1000 genomes]
rs11098895	0.83[AMR][1000 genomes]
rs12507438	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12642632	0.83[AMR][1000 genomes]
rs12645687	0.82[ASN][1000 genomes]
rs12646282	0.83[ASN][1000 genomes]
rs12649784	0.95[CEU][hapmap];0.85[CHB][hapmap];0.83[AMR][1000 genomes]
rs13122470	0.83[ASN][1000 genomes]
rs13152329	0.88[ASN][1000 genomes]
rs13152790	0.83[ASN][1000 genomes]
rs1472702	0.89[ASN][1000 genomes]
rs1503609	0.93[ASN][1000 genomes]
rs1503613	0.95[ASN][1000 genomes]
rs1503632	0.90[ASN][1000 genomes]
rs1503634	0.89[ASN][1000 genomes]
rs16997944	0.90[ASN][1000 genomes]
rs1847345	0.81[AMR][1000 genomes]
rs1948826	0.94[ASN][1000 genomes]
rs2089063	0.85[ASN][1000 genomes]
rs2102215	0.85[ASN][1000 genomes]
rs2202279	0.82[ASN][1000 genomes]
rs2391100	0.83[AMR][1000 genomes]
rs55832124	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs56261161	0.83[AMR][1000 genomes]
rs56807249	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs59656578	0.81[ASN][1000 genomes]
rs60076307	0.84[AMR][1000 genomes]
rs60860289	0.84[AMR][1000 genomes]
rs62322183	0.84[AMR][1000 genomes]
rs62322221	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6855733	0.82[ASN][1000 genomes]
rs72675928	0.80[ASN][1000 genomes]
rs7665607	0.83[AMR][1000 genomes]
rs7695444	0.81[AMR][1000 genomes]
rs7696279	0.83[AMR][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	nsv879909	chr4:127646765-127792639	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv879910	chr4:127646765-127805466	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv879911	chr4:127646765-127835677	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv879912	chr4:127706053-127775563	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3367258	chr4:127749396-127772702	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv428773	chr4:127760014-127913973	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127765200-127771600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:127767400-127770600	Weak transcription	HMEC	breast
3	chr4:127767600-127770600	Weak transcription	K562	blood
4	chr4:127770000-127770200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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