Variant report

Variant	rs7111913
Chromosome Location	chr11:75419003-75419004
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:75297859..75300646-chr11:75417581..75420277,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10160335	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs10160495	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs11236475	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs11236480	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs12279672	0.92[EUR][1000 genomes]
rs12281880	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs12282340	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs12294083	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12574289	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12574551	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12576145	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12576629	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12576635	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12577202	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17134189	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs17134192	0.89[EUR][1000 genomes]
rs17134210	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs17134231	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17134235	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2009247	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs3862804	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs4544029	0.89[EUR][1000 genomes]
rs57777945	0.89[EUR][1000 genomes]
rs61895122	0.81[EUR][1000 genomes]
rs61895124	0.89[EUR][1000 genomes]
rs61895125	0.89[EUR][1000 genomes]
rs61895126	0.89[EUR][1000 genomes]
rs61895128	0.89[EUR][1000 genomes]
rs61895131	0.89[EUR][1000 genomes]
rs61895132	0.89[EUR][1000 genomes]
rs61895133	0.89[EUR][1000 genomes]
rs61895134	0.89[EUR][1000 genomes]
rs61895137	0.89[EUR][1000 genomes]
rs61895139	0.89[EUR][1000 genomes]
rs61895140	0.89[EUR][1000 genomes]
rs61895141	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61895142	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61895143	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61897960	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7128429	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs73488490	0.92[EUR][1000 genomes]
rs73488497	0.92[EUR][1000 genomes]
rs73502466	0.95[EUR][1000 genomes]
rs7482921	0.84[EUR][1000 genomes]

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	esv3381903	chr11:75123498-75587233	Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75417400-75419200	Weak transcription	Right Atrium	heart
2	chr11:75417800-75423800	Weak transcription	Colonic Mucosa	Colon
3	chr11:75417800-75424000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr11:75418400-75419200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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