Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:25764701..25766710-chr10:25768952..25770466,2	K562	blood:

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

rs_ID	r²[population]
rs10828809	1.00[EUR][1000 genomes]
rs11014525	1.00[CEU][hapmap]
rs12249673	1.00[EUR][1000 genomes]
rs12259717	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12263407	1.00[CEU][hapmap]
rs12267402	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12781894	1.00[CEU][hapmap]
rs1329253	1.00[CEU][hapmap]
rs16926013	1.00[CEU][hapmap]
rs16926017	1.00[CEU][hapmap]
rs16926019	1.00[CEU][hapmap]
rs59780253	1.00[EUR][1000 genomes]
rs6482486	1.00[CEU][hapmap]
rs6482487	1.00[CEU][hapmap]
rs7085469	1.00[CEU][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73608302	1.00[EUR][1000 genomes]
rs73610305	1.00[EUR][1000 genomes]
rs73610306	1.00[EUR][1000 genomes]
rs7907745	1.00[EUR][1000 genomes]
rs7907884	1.00[EUR][1000 genomes]
rs7912976	1.00[EUR][1000 genomes]
rs7915434	1.00[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	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25756800-25775000	Weak transcription	K562	blood
2	chr10:25757200-25769600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr10:25765600-25766000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr10:25765800-25770000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr10:25765800-25782800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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