Variant report

Variant	rs4902812
Chromosome Location	chr14:70752703-70752704
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10134376	0.86[CHB][hapmap]
rs10140161	0.86[CHB][hapmap]
rs10140916	0.86[CHB][hapmap]
rs10140938	0.82[CHB][hapmap]
rs10141034	0.86[CHB][hapmap]
rs10142875	0.82[CHB][hapmap]
rs10150618	0.82[CHB][hapmap]
rs10220380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11158856	0.86[CHB][hapmap]
rs11620731	0.86[CHB][hapmap]
rs12431557	0.86[CHB][hapmap]
rs12433437	0.86[CHB][hapmap]
rs12434413	0.86[CHB][hapmap]
rs12588332	0.86[CHB][hapmap]
rs2275297	0.85[CHB][hapmap]
rs2275298	0.86[CHB][hapmap]
rs2332278	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2332279	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2332281	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2332363	0.86[CHB][hapmap]
rs2332364	0.86[CHB][hapmap]
rs2332418	0.86[CHB][hapmap]
rs2332419	0.85[CHB][hapmap]
rs2332420	0.86[CHB][hapmap]
rs2332422	0.86[CHB][hapmap]
rs2877659	0.86[CHB][hapmap]
rs2877670	0.86[CHB][hapmap]
rs3784155	0.85[CHB][hapmap]
rs4331283	0.90[MEX][hapmap];0.92[TSI][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4600398	0.85[CHB][hapmap]
rs4749	0.86[CHB][hapmap]
rs4899343	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902811	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6420899	0.85[CHB][hapmap]
rs6573950	0.85[CHB][hapmap]
rs6573951	0.86[CHB][hapmap]
rs6573952	0.85[CHB][hapmap]
rs6573953	0.86[CHB][hapmap]
rs6573954	0.86[CHB][hapmap]
rs6573956	0.86[CHB][hapmap]
rs6573957	0.86[CHB][hapmap]
rs7144850	0.86[CHB][hapmap]
rs7148889	0.86[CHB][hapmap]
rs7155332	0.86[CHB][hapmap]
rs7155763	0.86[CHB][hapmap]
rs7157399	0.82[CHB][hapmap]
rs7157430	0.86[CHB][hapmap]
rs8017274	0.84[CHB][hapmap]
rs8018531	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9323537	0.85[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902075	chr14:70612618-70919016	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4902812	PAPLN	cis	parietal	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70749400-70758400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:70749600-70756800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr14:70750200-70755600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr14:70750200-70757800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr14:70752600-70753400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links