Variant report

Variant	rs2357678
Chromosome Location	chr6:120102321-120102322
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:120100263..120103492-chr6:120105625..120107815,3	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1156148	0.83[EUR][1000 genomes]
rs12197190	0.80[EUR][1000 genomes]
rs1341501	0.82[CHB][hapmap]
rs1417842	0.80[EUR][1000 genomes]
rs1417844	0.82[EUR][1000 genomes]
rs1417845	0.82[EUR][1000 genomes]
rs1884254	0.84[EUR][1000 genomes]
rs1884256	0.81[CHB][hapmap]
rs2207611	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs4310086	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4946435	0.81[EUR][1000 genomes]
rs6569085	0.82[EUR][1000 genomes]
rs6569088	0.82[ASN][1000 genomes]
rs6569089	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6899335	0.81[EUR][1000 genomes]
rs6922103	0.82[ASN][1000 genomes]
rs7739068	0.85[ASN][1000 genomes]
rs7739078	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7747886	0.82[ASN][1000 genomes]
rs7763039	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7771532	0.82[ASN][1000 genomes]
rs9372550	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9372551	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9372553	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9374815	0.81[EUR][1000 genomes]
rs9374819	0.81[EUR][1000 genomes]
rs9374826	0.85[ASN][1000 genomes]
rs9374827	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9387675	0.84[CEU][hapmap];0.84[EUR][1000 genomes]
rs9387678	0.82[ASN][1000 genomes]
rs9387679	0.82[ASN][1000 genomes]
rs9387681	0.82[EUR][1000 genomes]
rs9398521	0.81[EUR][1000 genomes]
rs9398527	0.85[ASN][1000 genomes]
rs9401163	0.81[EUR][1000 genomes]
rs9401171	0.82[EUR][1000 genomes]
rs9481954	0.80[EUR][1000 genomes]
rs9489766	0.80[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	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:120101400-120102600	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr6:120101400-120102800	Enhancers	Dnd41	blood
3	chr6:120102200-120102600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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