Variant report

Variant	rs4769681
Chromosome Location	chr13:29699041-29699042
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1109007	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1887749	0.86[ASN][1000 genomes]
rs1927838	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1927840	0.81[ASN][1000 genomes]
rs1952421	0.87[ASN][1000 genomes]
rs2025972	0.82[ASN][1000 genomes]
rs4238115	0.81[ASN][1000 genomes]
rs4365146	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4432107	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4769002	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6490355	0.81[ASN][1000 genomes]
rs7331539	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7331934	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7332351	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7994936	0.81[ASN][1000 genomes]
rs7999357	0.86[ASN][1000 genomes]
rs7999521	0.86[ASN][1000 genomes]
rs9508281	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9508284	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9508285	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9508288	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9579284	0.83[ASN][1000 genomes]
rs9579290	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[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	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv3406145	chr13:29616606-29917459	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr13:29692600-29703400	Weak transcription	Aorta	Aorta
2	chr13:29692600-29703800	Weak transcription	Left Ventricle	heart
3	chr13:29692600-29705600	Weak transcription	Right Ventricle	heart
4	chr13:29697800-29699200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr13:29697800-29700200	Enhancers	Fetal Heart	heart
6	chr13:29698200-29699800	Enhancers	Liver	Liver
7	chr13:29698600-29699600	Enhancers	Primary T cells from cord blood	blood
8	chr13:29698800-29699400	Enhancers	Dnd41	blood
9	chr13:29698800-29699600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr13:29699000-29699200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr13:29699000-29699400	Enhancers	GM12878-XiMat	blood
12	chr13:29699000-29699600	Enhancers	Rectal Smooth Muscle	rectum
13	chr13:29699000-29700000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr13:29699000-29700600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr13:29699000-29700600	Enhancers	Primary B cells from peripheral blood	blood
16	chr13:29699000-29701400	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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