Variant report

No.	Distal block	Cell Line	Cell type
1	chr6:11944959..11946761-chr6:12016853..12018812,2	K562	blood:
2	chr6:11945990..11949036-chr6:11950804..11953646,3	K562	blood:
3	chr6:11928396..11930237-chr6:11946465..11949444,2	K562	blood:
4	chr6:11946393..11948154-chr6:11992265..11994588,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12193434	0.89[EUR][1000 genomes]
rs16872077	1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs16872108	0.91[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs169716	0.86[EUR][1000 genomes]
rs17533974	1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs209778	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs209808	0.89[EUR][1000 genomes]
rs209811	0.86[EUR][1000 genomes]
rs61128649	0.83[ASN][1000 genomes]
rs6901986	0.83[ASN][1000 genomes]
rs6905403	0.93[ASN][1000 genomes]
rs6919025	0.83[ASN][1000 genomes]
rs6927887	0.85[ASN][1000 genomes]
rs6928723	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7775818	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs9296237	1.00[JPT][hapmap]
rs9380630	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs9380639	0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9394442	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs9394473	1.00[JPT][hapmap]

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	esv2427616	chr6:11945409-11946714	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11944600-11946800	Weak transcription	K562	blood
2	chr6:11946000-11947800	Weak transcription	Liver	Liver

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