Variant report

Variant	rs17036480
Chromosome Location	chr4:106922483-106922484
allele	A/G
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:46)

rs_ID	r²[population]
rs1108244	1.00[ASN][1000 genomes]
rs1108245	1.00[ASN][1000 genomes]
rs1108246	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12500199	0.94[ASN][1000 genomes]
rs13128995	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17036424	0.92[ASN][1000 genomes]
rs17036425	0.99[ASN][1000 genomes]
rs17036491	0.94[ASN][1000 genomes]
rs17036492	0.94[ASN][1000 genomes]
rs1893715	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1893716	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2156507	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2866784	0.81[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2866785	0.99[ASN][1000 genomes]
rs28790999	0.87[ASN][1000 genomes]
rs28798389	0.89[ASN][1000 genomes]
rs34855241	0.91[ASN][1000 genomes]
rs35019375	0.81[ASN][1000 genomes]
rs35341779	0.91[ASN][1000 genomes]
rs35686571	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35716368	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4142419	0.94[ASN][1000 genomes]
rs4277780	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4345186	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4345187	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4585305	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4698952	0.80[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs4699206	0.80[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs4699207	0.80[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs6533233	0.95[ASN][1000 genomes]
rs6812365	0.80[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs6813376	0.81[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs71599091	0.91[ASN][1000 genomes]
rs72958841	0.96[ASN][1000 genomes]
rs72958868	0.80[AFR][1000 genomes]
rs869929	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs884691	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs915880	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs915881	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs959786	1.00[ASN][1000 genomes]
rs959787	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9683620	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9683630	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9683643	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9683650	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9684387	1.00[ASN][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	nsv1014993	chr4:106796019-106980727	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv522792	chr4:106895964-106982793	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106907800-106925000	Weak transcription	Pancreas	Pancrea
2	chr4:106919800-106924200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:106921000-106924200	Weak transcription	HepG2	liver
4	chr4:106921200-106923600	Weak transcription	Fetal Kidney	kidney
5	chr4:106922200-106922600	Enhancers	Fetal Stomach	stomach
6	chr4:106922200-106923200	Enhancers	Colon Smooth Muscle	Colon

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