Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EBF1	chr14:71685047-71685310	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000269945	TF binding region
ENSG00000267901	TF binding region

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10144392	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17177822	0.84[CEU][hapmap]
rs17767266	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs17767296	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1990035	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs4899390	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4902887	1.00[CHB][hapmap]
rs4902916	0.83[CEU][hapmap]
rs4902922	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55737377	0.80[AMR][1000 genomes]
rs60526802	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61989206	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61989207	0.84[AMR][1000 genomes]
rs61989208	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6574006	0.83[CEU][hapmap]
rs6574007	0.85[CEU][hapmap]
rs7146169	0.94[CEU][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7153194	0.82[AMR][1000 genomes]
rs72726677	0.84[AMR][1000 genomes]
rs8005089	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs8010203	0.84[CEU][hapmap]
rs8017895	0.81[AMR][1000 genomes];0.92[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	nsv1041980	chr14:71196358-71767339	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv542125	chr14:71196358-71767339	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1044090	chr14:71496198-71780026	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv832827	chr14:71676178-71833519	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71680600-71702600	Weak transcription	Brain Angular Gyrus	brain
2	chr14:71680800-71691600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr14:71680800-71691800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr14:71682400-71687200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:71682600-71694800	Weak transcription	Pancreas	Pancrea
6	chr14:71684800-71686200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr14:71685000-71685400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr14:71685000-71685400	Enhancers	Osteobl	bone
9	chr14:71685000-71687000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr14:71685200-71686600	Weak transcription	Spleen	Spleen

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