Variant report

Variant	rs595864
Chromosome Location	chr6:13251072-13251073
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:13244619..13246352-chr6:13250637..13252515,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10948561	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11757292	0.84[YRI][hapmap]
rs11968818	0.85[JPT][hapmap]
rs12525892	1.00[ASN][1000 genomes]
rs12525906	1.00[ASN][1000 genomes]
rs12527600	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529141	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12665408	0.94[ASN][1000 genomes]
rs1569418	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs16873893	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1706941	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1736501	1.00[ASN][1000 genomes]
rs1736502	1.00[CHB][hapmap];0.85[JPT][hapmap];0.98[ASN][1000 genomes]
rs1937765	0.94[ASN][1000 genomes]
rs202024	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs202026	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs202055	0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs202058	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs202059	0.86[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs202067	0.87[CEU][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes]
rs34373947	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs393032	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs396360	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs413167	0.85[CHB][hapmap];0.85[JPT][hapmap];1.00[ASN][1000 genomes]
rs416852	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs426518	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs428975	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs429919	1.00[ASN][1000 genomes]
rs429935	1.00[ASN][1000 genomes]
rs430216	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs434703	1.00[ASN][1000 genomes]
rs436268	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs436490	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs443150	1.00[ASN][1000 genomes]
rs4711945	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4711948	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4711949	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4711956	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4715157	0.85[JPT][hapmap]
rs4715159	0.85[JPT][hapmap]
rs4715168	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4715174	0.85[JPT][hapmap]
rs521960	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs527857	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs533512	1.00[ASN][1000 genomes]
rs534266	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs534404	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs534449	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs546673	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs555496	0.92[ASN][1000 genomes]
rs58474010	0.90[ASN][1000 genomes]
rs7759256	1.00[CEU][hapmap];0.85[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7763251	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7765972	0.86[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432849	chr6:13225077-13253733	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv532021	chr6:13232627-13805381	Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
3	nsv1028533	chr6:13239059-13484814	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv538136	chr6:13239059-13484814	Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv981320	chr6:13247460-13253055	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1034016	chr6:13248122-13418225	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs595864	PHACTR1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13230600-13253400	Weak transcription	Spleen	Spleen
2	chr6:13233200-13256000	Weak transcription	Right Ventricle	heart
3	chr6:13234600-13267200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:13237600-13252800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr6:13239000-13253200	Weak transcription	Aorta	Aorta
6	chr6:13240200-13251200	Weak transcription	Left Ventricle	heart
7	chr6:13241600-13251200	Weak transcription	Stomach Smooth Muscle	stomach
8	chr6:13242800-13256000	Weak transcription	Pancreas	Pancrea
9	chr6:13248600-13256600	Weak transcription	Brain Hippocampus Middle	brain
10	chr6:13248600-13260200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr6:13248800-13256200	Weak transcription	Brain Germinal Matrix	brain
12	chr6:13248800-13266600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:13249000-13257800	Weak transcription	Brain Anterior Caudate	brain
14	chr6:13249000-13266000	Weak transcription	Fetal Brain Female	brain
15	chr6:13249200-13251200	Weak transcription	Lung	lung
16	chr6:13249200-13253600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:13249200-13254400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr6:13249200-13272200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr6:13249600-13252200	Weak transcription	Fetal Muscle Leg	muscle
20	chr6:13249600-13256400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:13249800-13287000	Weak transcription	Fetal Brain Male	brain
22	chr6:13250200-13251200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:13250200-13251600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:13250600-13251600	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr6:13250800-13251200	Enhancers	HepG2	liver
26	chr6:13250800-13251400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr6:13250800-13251600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr6:13251000-13251200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:13251000-13251800	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr6:13251000-13253000	Weak transcription	Primary B cells from peripheral blood	blood
31	chr6:13251000-13253000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:13251000-13253200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr6:13251000-13253200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr6:13251000-13259000	Weak transcription	Fetal Heart	heart

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