Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:32431985..32434925-chr11:32436480..32438156,2	K562	blood:
2	chr11:32431798..32437144-chr11:32439795..32446613,10	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs16923250	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17673047	1.00[JPT][hapmap]
rs1799933	1.00[CHB][hapmap]
rs2234588	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2234593	1.00[JPT][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes]
rs5030166	1.00[CHB][hapmap]
rs5030188	1.00[ASN][1000 genomes]
rs5030194	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030195	0.90[AFR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030219	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030228	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5030255	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs5030278	1.00[JPT][hapmap]
rs5030302	1.00[JPT][hapmap]
rs5030311	1.00[JPT][hapmap]
rs5030315	1.00[JPT][hapmap]
rs5030316	1.00[JPT][hapmap]
rs5030335	1.00[JPT][hapmap];0.86[YRI][hapmap];0.89[AFR][1000 genomes]
rs59961456	0.84[AFR][1000 genomes]
rs7105471	0.84[AFR][1000 genomes]
rs7120483	0.88[AFR][1000 genomes]
rs72893506	0.81[ASN][1000 genomes]
rs73473736	0.92[AFR][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	nsv832108	chr11:32395937-32560583	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1038188	chr11:32410305-32449799	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32427800-32435000	Weak transcription	K562	blood
2	chr11:32433400-32437200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr11:32434000-32442400	Weak transcription	Right Ventricle	heart
4	chr11:32434200-32438000	Weak transcription	Ovary	ovary
5	chr11:32434400-32435400	Strong transcription	Fetal Kidney	kidney

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