Variant report

Variant	rs9444837
Chromosome Location	chr6:91951308-91951309
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs17605336	1.00[EUR][1000 genomes]
rs17667431	1.00[EUR][1000 genomes]
rs58594683	1.00[AMR][1000 genomes]
rs59941830	1.00[EUR][1000 genomes]
rs73518444	1.00[AMR][1000 genomes]
rs73520536	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73520569	1.00[EUR][1000 genomes]
rs73520587	1.00[EUR][1000 genomes]
rs73520596	1.00[EUR][1000 genomes]
rs73520597	1.00[EUR][1000 genomes]
rs73520598	1.00[EUR][1000 genomes]
rs73520600	1.00[EUR][1000 genomes]
rs73522303	1.00[EUR][1000 genomes]
rs73522307	1.00[EUR][1000 genomes]
rs9444853	1.00[EUR][1000 genomes]
rs9451645	1.00[EUR][1000 genomes]
rs9451648	1.00[EUR][1000 genomes]
rs9451650	1.00[EUR][1000 genomes]
rs9451651	1.00[EUR][1000 genomes]
rs9451652	1.00[EUR][1000 genomes]
rs9451653	1.00[EUR][1000 genomes]
rs9451655	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752130	chr6:91740447-92196479	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1031681	chr6:91784557-92075312	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv538359	chr6:91784557-92075312	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1017467	chr6:91802015-92417554	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
5	nsv538360	chr6:91802015-92417554	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
6	esv2422475	chr6:91818508-91998748	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	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	chr6:91951000-91951400	Enhancers	Fetal Stomach	stomach
2	chr6:91951000-91952400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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