Variant report

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

rs_ID	r²[population]
rs10508693	1.00[CHB][hapmap]
rs12357174	1.00[CHB][hapmap]
rs1335195	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes]
rs1335197	1.00[CHB][hapmap]
rs16926121	0.90[EUR][1000 genomes]
rs16926124	1.00[CHB][hapmap]
rs16926153	1.00[CHB][hapmap];0.86[EUR][1000 genomes]
rs16926158	0.86[EUR][1000 genomes]
rs16926172	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes]
rs17628278	1.00[CHB][hapmap]
rs2001385	0.86[EUR][1000 genomes]
rs2026055	1.00[CHB][hapmap]
rs4523593	1.00[CHB][hapmap]
rs4747532	1.00[CHB][hapmap]
rs6482497	1.00[CHB][hapmap]
rs6482498	1.00[CHB][hapmap]
rs6482499	1.00[CHB][hapmap]
rs73610307	0.82[EUR][1000 genomes]
rs74124215	0.86[EUR][1000 genomes]
rs7909167	0.86[EUR][1000 genomes]
rs7911892	1.00[CHB][hapmap];0.90[EUR][1000 genomes]
rs7921299	1.00[CHB][hapmap]

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	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
2	nsv894972	chr10:25849998-25917909	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25861600-25873800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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