Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:74117628..74120128-chr6:74125785..74127778,2	K562	blood:

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1066686	1.00[AMR][1000 genomes]
rs11961485	1.00[EUR][1000 genomes]
rs11962073	1.00[EUR][1000 genomes]
rs11964811	1.00[EUR][1000 genomes]
rs311687	1.00[AMR][1000 genomes]
rs471125	1.00[AMR][1000 genomes]
rs472956	1.00[AMR][1000 genomes]
rs489006	1.00[AMR][1000 genomes]
rs497243	1.00[AMR][1000 genomes]
rs505344	1.00[AMR][1000 genomes]
rs520570	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs528895	1.00[AMR][1000 genomes]
rs531672	1.00[EUR][1000 genomes]
rs562270	1.00[EUR][1000 genomes]
rs571304	1.00[AMR][1000 genomes]
rs571508	1.00[ASW][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs577250	1.00[EUR][1000 genomes]
rs58857515	1.00[EUR][1000 genomes]
rs59903417	1.00[EUR][1000 genomes]
rs6905319	1.00[EUR][1000 genomes]
rs73450693	1.00[EUR][1000 genomes]
rs73452548	1.00[EUR][1000 genomes]
rs73754636	1.00[EUR][1000 genomes]
rs73754640	1.00[EUR][1000 genomes]
rs7750842	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9350496	0.80[AFR][1000 genomes]
rs9442927	1.00[EUR][1000 genomes]
rs9446898	1.00[AMR][1000 genomes]
rs9446934	1.00[EUR][1000 genomes]
rs9446936	1.00[EUR][1000 genomes]
rs9446937	1.00[EUR][1000 genomes]
rs966427	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3410973	chr6:73716033-74419545	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv830693	chr6:74049342-74216080	Flanking Active TSS Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74115000-74131000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr6:74115800-74131200	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr6:74117200-74120400	Strong transcription	Placenta	Placenta
4	chr6:74117400-74123000	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr6:74117800-74131800	Weak transcription	Primary B cells from cord blood	blood
6	chr6:74118600-74125600	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr6:74119000-74119200	Enhancers	Fetal Intestine Large	intestine
8	chr6:74119000-74119400	Enhancers	HepG2	liver
9	chr6:74119000-74119800	Enhancers	Small Intestine	intestine

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