Variant report

Variant	rs34934295
Chromosome Location	chr6:15195265-15195266
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:15194327..15197318-chr6:15210091..15212891,2	K562	blood:
2	chr6:15177562..15179581-chr6:15194132..15195996,2	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs13191127	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13197919	0.88[EUR][1000 genomes]
rs13198600	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13201343	0.85[EUR][1000 genomes]
rs13206138	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13206695	0.93[EUR][1000 genomes]
rs13209122	1.00[EUR][1000 genomes]
rs13209721	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13210652	0.92[EUR][1000 genomes]
rs13213534	0.93[EUR][1000 genomes]
rs13215638	0.93[EUR][1000 genomes]
rs13216551	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13216625	0.93[EUR][1000 genomes]
rs13219748	1.00[EUR][1000 genomes]
rs34048058	0.92[EUR][1000 genomes]
rs34144528	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34156913	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34229995	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34340185	0.88[EUR][1000 genomes]
rs34390534	1.00[EUR][1000 genomes]
rs34470245	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34488826	0.92[EUR][1000 genomes]
rs34677259	1.00[EUR][1000 genomes]
rs34790337	0.92[EUR][1000 genomes]
rs34816087	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34816488	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35147300	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35378362	1.00[EUR][1000 genomes]
rs35468212	0.85[EUR][1000 genomes]
rs35659244	0.93[EUR][1000 genomes]
rs35660009	0.93[EUR][1000 genomes]
rs35981238	1.00[EUR][1000 genomes]
rs67845400	0.93[EUR][1000 genomes]
rs71533639	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71533640	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71533642	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71551024	0.85[EUR][1000 genomes]
rs71551025	1.00[EUR][1000 genomes]
rs71551028	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71551030	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71551032	1.00[EUR][1000 genomes]
rs71551033	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71551034	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71551035	0.96[EUR][1000 genomes]
rs71551040	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71551041	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71551042	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs71551043	0.88[EUR][1000 genomes]
rs71551045	0.88[EUR][1000 genomes]
rs71551046	0.88[EUR][1000 genomes]
rs7740407	1.00[EUR][1000 genomes]
rs9383028	0.93[EUR][1000 genomes]
rs9476760	0.93[EUR][1000 genomes]
rs9476761	0.93[EUR][1000 genomes]
rs9476782	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9476783	1.00[EUR][1000 genomes]
rs9476784	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9476790	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9476793	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9476794	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9476797	1.00[EUR][1000 genomes]
rs9476798	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830593	chr6:15049636-15244190	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv830594	chr6:15171158-15261296	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	esv1011225	chr6:15188151-15198037	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15193600-15195400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:15194000-15195400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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