Variant report

Variant	rs72972364
Chromosome Location	chr11:93122128-93122129
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10466368	0.81[EUR][1000 genomes]
rs11601056	0.82[EUR][1000 genomes]
rs11604909	0.82[EUR][1000 genomes]
rs1456238	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1869914	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1975820	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2259633	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2605574	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2605580	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2605581	0.90[EUR][1000 genomes]
rs2605611	0.81[EUR][1000 genomes]
rs2658773	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2658775	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2658791	0.87[EUR][1000 genomes]
rs2925355	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2925362	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2925938	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3019205	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3019206	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3019221	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3019222	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3019223	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3020057	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3020073	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3020076	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56091149	0.84[EUR][1000 genomes]
rs7116173	0.81[EUR][1000 genomes]
rs72972357	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039134	chr11:92790000-93219942	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv468793	chr11:93068163-93129893	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
4	nsv1035530	chr11:93114111-93148948	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs72972364	CCDC67	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93111200-93128200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:93116600-93122400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:93116800-93126000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:93118600-93124600	Weak transcription	Aorta	Aorta
5	chr11:93121000-93130200	Weak transcription	K562	blood

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