Variant report

Variant	rs568694
Chromosome Location	chr13:91784921-91784922
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:91784421..91786041-chr13:92003504..92005785,2	K562	blood:

Variant related genes	Relation type
ENSG00000215417	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs1020800	0.85[EUR][1000 genomes]
rs1020801	0.85[EUR][1000 genomes]
rs1174782	0.88[EUR][1000 genomes]
rs1174784	0.85[EUR][1000 genomes]
rs1332218	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs148771	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs167003	0.96[EUR][1000 genomes]
rs16952571	0.96[EUR][1000 genomes]
rs287490	0.91[EUR][1000 genomes]
rs287491	0.89[EUR][1000 genomes]
rs287492	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs287493	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs287494	0.93[EUR][1000 genomes]
rs287495	0.92[EUR][1000 genomes]
rs287496	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs287497	0.90[EUR][1000 genomes]
rs287498	0.90[EUR][1000 genomes]
rs287499	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs287500	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs287501	0.93[EUR][1000 genomes]
rs287502	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs287504	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs287505	0.93[EUR][1000 genomes]
rs287506	0.94[EUR][1000 genomes]
rs287508	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs287509	0.94[EUR][1000 genomes]
rs287510	0.94[EUR][1000 genomes]
rs287511	0.94[EUR][1000 genomes]
rs287512	0.94[EUR][1000 genomes]
rs287513	0.94[EUR][1000 genomes]
rs287514	0.96[EUR][1000 genomes]
rs287515	0.94[EUR][1000 genomes]
rs287516	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs287517	0.96[EUR][1000 genomes]
rs287518	0.96[EUR][1000 genomes]
rs287522	0.96[EUR][1000 genomes]
rs287523	0.96[EUR][1000 genomes]
rs287524	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs287525	0.92[EUR][1000 genomes]
rs287526	0.96[EUR][1000 genomes]
rs287527	0.98[EUR][1000 genomes]
rs287528	0.96[EUR][1000 genomes]
rs287529	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs287535	0.82[EUR][1000 genomes]
rs3764129	0.88[EUR][1000 genomes]
rs476066	0.82[EUR][1000 genomes]
rs481037	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs492117	0.85[EUR][1000 genomes]
rs504180	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs505160	0.85[EUR][1000 genomes]
rs506173	0.85[EUR][1000 genomes]
rs506238	0.85[EUR][1000 genomes]
rs512524	0.85[EUR][1000 genomes]
rs515029	0.85[EUR][1000 genomes]
rs515097	0.85[EUR][1000 genomes]
rs515850	0.85[EUR][1000 genomes]
rs521178	0.83[EUR][1000 genomes]
rs536365	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs538062	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs539504	0.85[EUR][1000 genomes]
rs543567	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs544464	0.85[EUR][1000 genomes]
rs549865	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs550731	0.83[EUR][1000 genomes]
rs558827	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs568455	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs571202	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs582256	0.96[EUR][1000 genomes]
rs583053	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs612195	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs613553	0.85[EUR][1000 genomes]
rs620620	0.88[EUR][1000 genomes]
rs622426	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs623637	0.85[EUR][1000 genomes]
rs644953	0.85[EUR][1000 genomes]
rs647785	0.85[EUR][1000 genomes]
rs650892	0.84[EUR][1000 genomes]
rs657464	0.85[EUR][1000 genomes]
rs665530	0.84[EUR][1000 genomes]
rs684050	0.85[EUR][1000 genomes]
rs693016	0.83[EUR][1000 genomes]
rs693721	0.85[EUR][1000 genomes]
rs7324853	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs76384	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs922083	0.85[EUR][1000 genomes]
rs9515887	0.96[EUR][1000 genomes]
rs9523263	0.85[EUR][1000 genomes]
rs9560762	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932206	chr13:91370888-91878374	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1042947	chr13:91571040-92416897	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
3	nsv541871	chr13:91571040-92416897	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
4	nsv900880	chr13:91625722-91848290	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv1803618	chr13:91669587-92277699	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1945 gene(s)	inside rSNPs	diseases
6	nsv900881	chr13:91704312-91829940	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1050259	chr13:91759549-92152078	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1944 gene(s)	inside rSNPs	diseases
8	nsv541872	chr13:91759549-92152078	Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1944 gene(s)	inside rSNPs	diseases
9	nsv832678	chr13:91771619-91932241	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr13:91778400-91786800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr13:91782800-91793800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:91784600-91785400	Enhancers	Fetal Lung	lung
4	chr13:91784600-91785600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr13:91784800-91785000	Enhancers	Fetal Brain Male	brain
6	chr13:91784800-91785200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links