Variant report

Variant	rs12429697
Chromosome Location	chr13:48355915-48355916
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10507561	0.85[CEU][hapmap]
rs12586040	0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap]
rs1924803	0.85[CEU][hapmap]
rs1924804	0.89[EUR][1000 genomes]
rs2077433	0.85[CEU][hapmap]
rs7326024	0.90[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7326753	0.84[CEU][hapmap]
rs9526395	0.84[CEU][hapmap]
rs9526396	0.84[CEU][hapmap]
rs9526399	0.91[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs9526400	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs9534831	0.90[EUR][1000 genomes]
rs9534832	0.89[EUR][1000 genomes]
rs9534834	0.89[EUR][1000 genomes]
rs9534835	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs9534836	0.89[EUR][1000 genomes]
rs9534856	1.00[YRI][hapmap]
rs9534857	1.00[YRI][hapmap]

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	esv3510679	chr13:48236624-48498185	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3510680	chr13:48236624-48498185	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv561589	chr13:48251736-48420218	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv561590	chr13:48350699-48399027	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs12429697	RCBTB1	cis	parietal	SCAN
rs12429697	CDADC1	cis	cerebellum	SCAN
rs12429697	LOC220429	cis	cerebellum	SCAN
rs12429697	CCDC122	cis	cerebellum	SCAN
rs12429697	RCBTB1	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:48350400-48356000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links