Variant report

Variant	rs4504214
Chromosome Location	chr4:30826506-30826507
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10006361	0.80[CEU][hapmap];0.96[CHB][hapmap];0.91[JPT][hapmap];0.87[YRI][hapmap];0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10008728	0.81[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs10021424	0.81[ASN][1000 genomes]
rs10024115	0.95[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs10517219	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10939312	0.82[ASN][1000 genomes]
rs11727285	0.80[AMR][1000 genomes]
rs12331633	0.82[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13108018	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1348921	0.95[CHB][hapmap];0.91[JPT][hapmap];0.86[YRI][hapmap];0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1374658	0.81[EUR][1000 genomes]
rs1447360	1.00[CEU][hapmap];0.91[YRI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1447364	0.91[CHB][hapmap];0.91[JPT][hapmap];0.87[YRI][hapmap];0.86[ASN][1000 genomes]
rs1447365	0.81[YRI][hapmap]
rs1486787	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs16884130	0.87[YRI][hapmap]
rs28716204	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35428738	0.82[ASN][1000 genomes]
rs4235010	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4368569	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4380480	0.91[CHB][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs4466008	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4498103	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4505780	0.91[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs4557224	0.85[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4611883	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4613528	0.83[ASN][1000 genomes]
rs4615135	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4619848	0.82[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4692105	0.91[CHB][hapmap];0.85[JPT][hapmap]
rs4995324	0.88[ASN][1000 genomes]
rs6448723	0.95[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs6812005	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs6815007	0.96[CHB][hapmap];0.91[JPT][hapmap]
rs6822350	0.89[EUR][1000 genomes]
rs6827723	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6828872	0.91[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs6832173	0.83[ASN][1000 genomes]
rs6844992	0.87[YRI][hapmap]
rs6855232	0.83[ASN][1000 genomes]
rs6855570	0.83[ASN][1000 genomes]
rs6856144	0.89[CHB][hapmap];0.91[JPT][hapmap];0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6858230	0.82[ASN][1000 genomes]
rs7654583	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7664926	0.83[ASN][1000 genomes]
rs7670155	0.96[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs7678055	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7685283	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7692210	0.90[CHB][hapmap];0.80[JPT][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7695488	0.96[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs9291549	0.91[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs9291550	0.87[YRI][hapmap]
rs9291553	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9999290	0.96[CHB][hapmap];0.91[JPT][hapmap];0.95[YRI][hapmap];0.80[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[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	nsv4285	chr4:30815642-30838784	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv499039	chr4:30819213-30830142	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	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
4	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:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30813800-30835800	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:30823800-30826600	Weak transcription	HUVEC	blood vessel
3	chr4:30823800-30827000	Weak transcription	Fetal Muscle Leg	muscle
4	chr4:30824200-30826800	Weak transcription	HSMM	muscle
5	chr4:30825200-30826800	Weak transcription	Hela-S3	cervix
6	chr4:30825200-30835800	Weak transcription	Aorta	Aorta
7	chr4:30826200-30827200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:30826400-30827200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:30826400-30827200	Enhancers	NH-A	brain
10	chr4:30826400-30830400	Weak transcription	Fetal Heart	heart

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