Variant report

Variant	rs10012637
Chromosome Location	chr4:30851743-30851744
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10006361	0.80[YRI][hapmap]
rs10010406	1.00[AMR][1000 genomes]
rs10013155	1.00[AMR][1000 genomes]
rs10014165	1.00[ASW][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.90[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10015789	0.85[YRI][hapmap];1.00[AMR][1000 genomes]
rs10019451	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10025381	0.87[ASW][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10026764	1.00[AMR][1000 genomes]
rs10026911	0.83[AMR][1000 genomes]
rs10028626	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10028966	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10034034	0.89[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10939319	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1348921	0.80[YRI][hapmap]
rs1447360	0.85[YRI][hapmap]
rs1447364	0.80[YRI][hapmap]
rs1447365	0.80[ASW][hapmap];0.85[YRI][hapmap]
rs16884130	0.90[YRI][hapmap];1.00[AMR][1000 genomes]
rs28363824	0.85[AMR][1000 genomes]
rs28408956	1.00[AMR][1000 genomes]
rs28441501	0.83[AMR][1000 genomes]
rs28534792	0.83[AMR][1000 genomes]
rs28593247	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28650136	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs28655825	0.83[AMR][1000 genomes]
rs28676746	1.00[AMR][1000 genomes]
rs57816723	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6812478	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6815248	1.00[ASW][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6823602	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6827169	0.84[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6844992	0.93[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9291550	0.90[YRI][hapmap];0.85[AMR][1000 genomes]
rs9884647	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9884648	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9997990	0.81[AFR][1000 genomes];1.00[AMR][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	nsv878810	chr4:30823157-30987395	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30842000-30854400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:30842400-30855200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:30842600-30854600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:30842600-30855800	Weak transcription	Aorta	Aorta
5	chr4:30846600-30855000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:30846800-30854600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:30849200-30854600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr4:30849200-30872200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:30850800-30855800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:30851000-30854000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:30851000-30854600	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr4:30851000-30855800	Weak transcription	Colon Smooth Muscle	Colon
13	chr4:30851000-30857800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr4:30851200-30851800	Weak transcription	Fetal Heart	heart
15	chr4:30851200-30854000	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr4:30851600-30855600	Weak transcription	NHLF	lung

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