Variant report

Variant	rs67325872
Chromosome Location	chr6:4663022-4663023
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11242965	0.82[ASN][1000 genomes]
rs11964064	0.80[EUR][1000 genomes]
rs12201817	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12201861	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12213814	0.97[EUR][1000 genomes]
rs1971444	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1971445	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2063677	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2063678	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2073042	0.96[EUR][1000 genomes]
rs2281275	0.96[EUR][1000 genomes]
rs443430	0.97[EUR][1000 genomes]
rs6918242	0.96[EUR][1000 genomes]
rs72819438	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs742570	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9328267	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9328268	0.97[EUR][1000 genomes]
rs9378408	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9392619	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9405760	0.97[EUR][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	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv528627	chr6:4614058-4731340	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4659000-4664200	Weak transcription	Right Ventricle	heart
2	chr6:4661000-4663400	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr6:4661200-4664200	Weak transcription	Right Atrium	heart
4	chr6:4661400-4664400	Weak transcription	Fetal Stomach	stomach
5	chr6:4661600-4664000	Weak transcription	Psoas Muscle	Psoas
6	chr6:4661600-4665000	Enhancers	Stomach Smooth Muscle	stomach
7	chr6:4661800-4663400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr6:4661800-4664400	Weak transcription	Spleen	Spleen
9	chr6:4661800-4664600	Weak transcription	Aorta	Aorta
10	chr6:4662000-4667200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:4662000-4667800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:4662400-4663200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:4662400-4664800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:4662600-4663200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr6:4662600-4663200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:4662600-4663600	Enhancers	HSMMtube	muscle
17	chr6:4662800-4663200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:4662800-4663200	Enhancers	Placenta	Placenta
19	chr6:4662800-4664200	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr6:4662800-4665000	Enhancers	Fetal Muscle Leg	muscle
21	chr6:4663000-4663200	Enhancers	NHLF	lung
22	chr6:4663000-4664000	Weak transcription	K562	blood
23	chr6:4663000-4664000	Weak transcription	Osteobl	bone
24	chr6:4663000-4664200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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