Variant report

Variant	rs35111535
Chromosome Location	chr11:114253747-114253748
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	chr11:114251835..114255649-chr11:114257498..114260898,3	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10457565	1.00[ASN][1000 genomes]
rs10457566	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12193575	1.00[ASN][1000 genomes]
rs12193685	1.00[ASN][1000 genomes]
rs12198862	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12200100	0.80[AMR][1000 genomes]
rs12202022	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12202345	1.00[ASN][1000 genomes]
rs12204522	1.00[ASN][1000 genomes]
rs12205351	0.80[AMR][1000 genomes]
rs12207007	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12210131	1.00[ASN][1000 genomes]
rs12211363	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12212907	1.00[ASN][1000 genomes]
rs12213224	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12214117	1.00[ASN][1000 genomes]
rs13191751	1.00[ASN][1000 genomes]
rs13193708	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13194156	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13199082	1.00[ASN][1000 genomes]
rs13205393	1.00[ASN][1000 genomes]
rs13214846	1.00[ASN][1000 genomes]
rs13218427	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13219477	1.00[ASN][1000 genomes]
rs34206551	1.00[ASN][1000 genomes]
rs34948572	1.00[ASN][1000 genomes]
rs35061946	1.00[ASN][1000 genomes]
rs35089988	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35916985	1.00[ASN][1000 genomes]
rs6935560	1.00[ASN][1000 genomes]
rs71572945	1.00[ASN][1000 genomes]
rs71572950	1.00[ASN][1000 genomes]
rs72989868	0.80[AMR][1000 genomes]
rs72989873	0.80[AMR][1000 genomes]
rs7760822	1.00[ASN][1000 genomes]
rs7767569	1.00[ASN][1000 genomes]
rs9885632	1.00[ASN][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	nsv949464	chr11:114186645-114480364	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv898396	chr11:114223577-114381972	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 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	chr11:114249200-114270400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:114250200-114255200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:114250400-114255200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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