Variant report

Variant	rs72722364
Chromosome Location	chr4:141846753-141846754
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10004141	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10004146	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10009037	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10009916	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11100687	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11726482	0.88[ASN][1000 genomes]
rs11732171	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11735133	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11735986	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11930379	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12503723	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12511709	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12642167	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12649305	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13104985	0.81[AMR][1000 genomes]
rs13111614	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13111885	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13120735	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13131785	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13135760	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13138724	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1425440	0.89[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1425441	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1425447	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1541735	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17338560	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17338710	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28445329	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4388161	0.86[EUR][1000 genomes]
rs60179902	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62345041	0.81[EUR][1000 genomes]
rs6537018	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6537019	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6537020	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6537021	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6827543	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6829247	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6838120	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6848867	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6856531	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7656504	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7662414	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7678079	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7683060	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7686712	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[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:36 , 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	chr4:141830200-141847600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:141832200-141855200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr4:141832600-141847800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr4:141842800-141852200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:141843200-141853400	Weak transcription	Fetal Brain Female	brain
9	chr4:141845600-141847000	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr4:141845600-141848000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:141845600-141848400	Enhancers	Fetal Heart	heart
12	chr4:141845600-141850000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr4:141845800-141846800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:141845800-141847000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:141845800-141847200	Strong transcription	Ovary	ovary
16	chr4:141846000-141846800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:141846000-141846800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:141846000-141846800	Genic enhancers	Spleen	Spleen
19	chr4:141846000-141847000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr4:141846000-141847000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:141846000-141847000	Genic enhancers	Fetal Muscle Leg	muscle
22	chr4:141846000-141847200	Strong transcription	Adipose Nuclei	Adipose
23	chr4:141846000-141847200	Enhancers	Psoas Muscle	Psoas
24	chr4:141846000-141847400	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr4:141846200-141846800	Enhancers	Fetal Thymus	thymus
26	chr4:141846200-141847200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr4:141846200-141847200	Strong transcription	Fetal Muscle Trunk	muscle
28	chr4:141846400-141847400	Genic enhancers	Right Ventricle	heart
29	chr4:141846400-141855200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:141846600-141847000	Genic enhancers	Colon Smooth Muscle	Colon
31	chr4:141846600-141847000	Genic enhancers	Fetal Stomach	stomach
32	chr4:141846600-141847200	Genic enhancers	Left Ventricle	heart
33	chr4:141846600-141847200	Genic enhancers	Stomach Smooth Muscle	stomach
34	chr4:141846600-141847600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr4:141846600-141849600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr4:141846600-141855600	Weak transcription	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links