Variant report

No.	Distal block	Cell Line	Cell type
1	chr10:22290815..22294027-chr10:22304843..22309151,5	K562	blood:
2	chr10:22303929..22306379-chr10:22718603..22721179,2	K562	blood:
3	chr10:22299405..22301907-chr10:22302576..22305786,3	MCF-7	breast:
4	chr10:22290901..22292656-chr10:22304512..22306179,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136770	Chromatin interaction

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11814448	0.82[EUR][1000 genomes]
rs11818726	0.90[EUR][1000 genomes]
rs12248406	0.82[EUR][1000 genomes]
rs16921919	0.82[EUR][1000 genomes]
rs55702118	0.89[EUR][1000 genomes]
rs55742770	1.00[EUR][1000 genomes]
rs55789720	0.89[EUR][1000 genomes]
rs56024469	0.89[EUR][1000 genomes]
rs56121502	0.89[EUR][1000 genomes]
rs56328322	0.89[EUR][1000 genomes]
rs66954116	0.89[EUR][1000 genomes]
rs67106981	0.89[EUR][1000 genomes]
rs67626393	0.89[EUR][1000 genomes]
rs7078177	0.82[EUR][1000 genomes]
rs72797462	1.00[EUR][1000 genomes]
rs72797470	1.00[EUR][1000 genomes]
rs72797476	1.00[EUR][1000 genomes]
rs72797490	0.89[EUR][1000 genomes]
rs72802957	0.89[EUR][1000 genomes]
rs72802961	0.89[EUR][1000 genomes]
rs72802964	0.89[EUR][1000 genomes]
rs72804398	0.90[EUR][1000 genomes]
rs72806334	1.00[EUR][1000 genomes]
rs72806949	1.00[EUR][1000 genomes]
rs72806951	0.82[EUR][1000 genomes]
rs72806987	0.97[AFR][1000 genomes]
rs72806995	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72806996	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72807000	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72807001	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72810732	0.89[EUR][1000 genomes]
rs72810741	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72810756	0.89[EUR][1000 genomes]
rs72810759	0.89[EUR][1000 genomes]
rs72810761	0.89[EUR][1000 genomes]
rs72810769	0.89[EUR][1000 genomes]
rs7912711	0.90[EUR][1000 genomes]

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	nsv831808	chr10:22187850-22357814	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr10:22299800-22305000	Weak transcription	Fetal Lung	lung
2	chr10:22300400-22305400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr10:22303600-22305800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr10:22303600-22306200	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr10:22303800-22305800	Enhancers	K562	blood
6	chr10:22304000-22306800	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr10:22304200-22305200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr10:22304200-22305400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr10:22304400-22305400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr10:22304600-22305800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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