Variant report

Variant	rs60179902
Chromosome Location	chr4:141836891-141836892
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10004141	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10004146	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10009037	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10009916	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11100687	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11726482	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11732171	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11735133	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11735986	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11930379	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12503723	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12511709	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12642167	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12649305	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13111614	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13111885	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13120735	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13131785	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13135760	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13138724	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1425440	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1425441	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1425447	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1541735	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17338560	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17338710	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28445329	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4388161	0.91[EUR][1000 genomes]
rs62345041	0.91[EUR][1000 genomes]
rs6537018	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6537019	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6537020	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6537021	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6827543	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6829247	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6838120	0.96[EUR][1000 genomes]
rs6848867	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6856531	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72722364	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7656504	0.93[EUR][1000 genomes]
rs7662414	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7678079	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7683060	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7686712	0.93[EUR][1000 genomes];0.80[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	nsv880167	chr4:141616979-142092124	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv830090	chr4:141770494-141947764	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830091	chr4:141796603-141980546	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv880168	chr4:141826780-141900370	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:141816200-141851400	Weak transcription	Brain Anterior Caudate	brain
2	chr4:141823200-141855800	Weak transcription	Osteobl	bone
3	chr4:141825800-141847200	Weak transcription	Fetal Kidney	kidney
4	chr4:141829600-141845600	Weak transcription	Fetal Heart	heart
5	chr4:141830200-141847600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr4:141832200-141845800	Weak transcription	Ovary	ovary
7	chr4:141832200-141846200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr4:141832200-141855200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr4:141832400-141846000	Weak transcription	Adipose Nuclei	Adipose
10	chr4:141832400-141846400	Weak transcription	Right Ventricle	heart
11	chr4:141832600-141846200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr4:141832600-141847800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr4:141833800-141846000	Weak transcription	Spleen	Spleen
14	chr4:141834000-141846200	Weak transcription	Colon Smooth Muscle	Colon
15	chr4:141834000-141846200	Weak transcription	Fetal Stomach	stomach
16	chr4:141836200-141837000	ZNF genes & repeats	Fetal Muscle Trunk	muscle
17	chr4:141836600-141837000	ZNF genes & repeats	Fetal Muscle Leg	muscle
18	chr4:141836800-141837000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr4:141836800-141837000	Weak transcription	Fetal Brain Female	brain
20	chr4:141836800-141837200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:141836800-141837200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr4:141836800-141845600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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