Variant report

Variant	rs34188562
Chromosome Location	chr3:42769974-42769975
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFK	chr3:42769965-42770190	HepG2	liver:	n/a	chr3:42770066-42770077 chr3:42770065-42770079
2	MAFK	chr3:42769939-42770139	HepG2	liver:	n/a	chr3:42770066-42770077 chr3:42770065-42770079

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:42746557..42750988-chr3:42768421..42772654,4	K562	blood:

Variant related genes	Relation type
CCDC13-AS1	TF binding region

Extended variants
information (count: 49 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs12485678	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12486439	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12487055	0.96[EUR][1000 genomes]
rs12488174	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12490743	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12492886	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12493321	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12495805	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13064320	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13072026	0.97[EUR][1000 genomes]
rs13085272	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13090185	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13095730	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1871121	0.92[ASN][1000 genomes]
rs2240860	0.97[EUR][1000 genomes]
rs2290972	0.83[ASN][1000 genomes]
rs2372111	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2372114	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs339693	0.86[ASN][1000 genomes]
rs339695	0.86[ASN][1000 genomes]
rs339696	0.86[ASN][1000 genomes]
rs34025253	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34482203	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34510173	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34648075	0.94[ASN][1000 genomes]
rs35389123	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35647815	0.92[ASN][1000 genomes]
rs35659560	0.97[EUR][1000 genomes]
rs35697625	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35766391	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36061398	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3912102	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3912103	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3916333	0.95[EUR][1000 genomes]
rs4488806	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55799024	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56232384	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56978598	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62246602	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62246607	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62250122	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66665035	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6765740	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6779396	0.97[EUR][1000 genomes]
rs6799524	0.80[ASN][1000 genomes]
rs7429327	0.92[ASN][1000 genomes]
rs7617368	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];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	nsv1013578	chr3:42747858-42817321	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv999713	chr3:42749022-42817321	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs34188562	CCDC13	cis	Thyroid	GTEx
rs34188562	CCDC13-AS1	cis	Thyroid	GTEx

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:42760400-42773600	Enhancers	Brain Substantia Nigra	brain
2	chr3:42763600-42773600	Enhancers	Brain Anterior Caudate	brain
3	chr3:42763600-42774800	Enhancers	Brain Angular Gyrus	brain
4	chr3:42763800-42771400	Weak transcription	Colon Smooth Muscle	Colon
5	chr3:42764000-42771000	Weak transcription	Psoas Muscle	Psoas
6	chr3:42765000-42771000	Weak transcription	Right Ventricle	heart
7	chr3:42765000-42772600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr3:42765200-42770800	Weak transcription	Fetal Heart	heart
9	chr3:42767600-42772600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr3:42767800-42774400	Enhancers	Brain Cingulate Gyrus	brain
11	chr3:42768600-42776000	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr3:42769000-42770000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr3:42769000-42770200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr3:42769000-42773600	Enhancers	Brain Hippocampus Middle	brain
15	chr3:42769000-42774200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr3:42769000-42774800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr3:42769000-42775000	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr3:42769600-42771200	Enhancers	Ovary	ovary
19	chr3:42769600-42785600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr3:42769800-42770200	Weak transcription	Left Ventricle	heart
21	chr3:42769800-42771000	Weak transcription	Adipose Nuclei	Adipose
22	chr3:42769800-42771000	Weak transcription	Right Atrium	heart
23	chr3:42769800-42773200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:42769800-42774200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr3:42769800-42787600	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links