Variant report

Variant	rs10021246
Chromosome Location	chr4:110829811-110829812
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:110829810-110829941	A549	lung:	n/a	n/a

Variant related genes	Relation type
EGF	TF binding region

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10000762	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs10002835	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10003648	1.00[EUR][1000 genomes]
rs10008969	1.00[CEU][hapmap]
rs10011256	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs10015673	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10018671	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10018709	1.00[EUR][1000 genomes]
rs10021699	1.00[CEU][hapmap]
rs10023766	1.00[EUR][1000 genomes]
rs10024160	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs10025706	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10027781	1.00[EUR][1000 genomes]
rs10028950	1.00[EUR][1000 genomes]
rs10029493	1.00[EUR][1000 genomes]
rs10029765	1.00[CEU][hapmap];0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10029774	1.00[EUR][1000 genomes]
rs10032001	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10034447	1.00[EUR][1000 genomes]
rs11569065	1.00[EUR][1000 genomes]
rs11569134	1.00[EUR][1000 genomes]
rs12331156	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12386405	1.00[EUR][1000 genomes]
rs17040963	1.00[CEU][hapmap]
rs17041311	1.00[CEU][hapmap]
rs17041322	1.00[CEU][hapmap]
rs1860131	1.00[CEU][hapmap]
rs28372160	1.00[EUR][1000 genomes]
rs28387677	1.00[EUR][1000 genomes]
rs28414645	1.00[EUR][1000 genomes]
rs28419786	1.00[EUR][1000 genomes]
rs28421711	1.00[EUR][1000 genomes]
rs28542074	1.00[EUR][1000 genomes]
rs28553469	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28592692	1.00[EUR][1000 genomes]
rs28599924	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28659909	1.00[EUR][1000 genomes]
rs28662394	1.00[EUR][1000 genomes]
rs28678255	1.00[EUR][1000 genomes]
rs28680960	1.00[EUR][1000 genomes]
rs28684716	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28687523	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28715029	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28719677	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28729403	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28733095	1.00[EUR][1000 genomes]
rs28780412	1.00[EUR][1000 genomes]
rs28803170	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28888150	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28889289	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28892978	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs41397647	1.00[EUR][1000 genomes]
rs41475346	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59590892	1.00[EUR][1000 genomes]
rs6533490	1.00[EUR][1000 genomes]
rs72896557	1.00[EUR][1000 genomes]
rs72898536	1.00[EUR][1000 genomes]
rs72898540	1.00[EUR][1000 genomes]
rs72898560	1.00[EUR][1000 genomes]
rs7442505	1.00[EUR][1000 genomes]
rs7668395	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs7691725	1.00[CEU][hapmap]
rs9307346	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9990841	1.00[CEU][hapmap]
rs9991664	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9992217	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9992709	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9993323	1.00[EUR][1000 genomes]
rs9994891	1.00[CEU][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	nsv530156	chr4:110721397-110911297	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr4:110825000-110834000	Weak transcription	Psoas Muscle	Psoas
2	chr4:110829800-110830400	Enhancers	Fetal Lung	lung

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