Variant report

Variant	rs35031559
Chromosome Location	chr8:100876705-100876706
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:100872705..100875370-chr8:100875936..100878606,2	K562	blood:
2	chr8:100871123..100872758-chr8:100876064..100877951,2	MCF-7	breast:
3	chr8:100872197..100874205-chr8:100875613..100878606,3	K562	blood:
4	chr8:100871760..100874701-chr8:100875723..100879242,3	MCF-7	breast:

Extended variants
information (count: 44 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10955222	0.86[ASN][1000 genomes]
rs1130474	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1130569	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1135382	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11987173	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12541837	0.82[ASN][1000 genomes]
rs12545930	0.81[EUR][1000 genomes]
rs12546882	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12548344	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12548542	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12548840	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13259051	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13260744	0.90[EUR][1000 genomes]
rs13264726	0.84[ASN][1000 genomes]
rs13265660	0.90[EUR][1000 genomes]
rs13271488	0.90[EUR][1000 genomes]
rs13274441	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34513504	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34830464	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35135010	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35769167	0.96[ASN][1000 genomes]
rs4409375	0.86[AMR][1000 genomes]
rs4434590	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4480092	0.81[ASN][1000 genomes]
rs4510829	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4626565	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62534626	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62534633	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6468694	0.86[ASN][1000 genomes]
rs6468695	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6468696	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6468697	0.95[ASN][1000 genomes]
rs6984511	0.82[ASN][1000 genomes]
rs7009713	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7157	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7812991	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7824037	0.90[EUR][1000 genomes]
rs7828241	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7831963	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7832488	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7840626	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7844439	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[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	nsv1033944	chr8:100737321-100916345	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv1830910	chr8:100791156-101114794	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking 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 miRNA target site	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs35031559	VPS13B	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100846400-100903800	Weak transcription	Stomach Mucosa	stomach
2	chr8:100850200-100887600	Weak transcription	Psoas Muscle	Psoas
3	chr8:100858600-100894000	Weak transcription	Fetal Brain Male	brain
4	chr8:100860200-100893000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr8:100860400-100887000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:100864800-100879800	Weak transcription	Small Intestine	intestine
7	chr8:100866200-100888000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr8:100866400-100880600	Weak transcription	GM12878-XiMat	blood
9	chr8:100867400-100879600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr8:100868600-100898400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr8:100869600-100883600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:100870400-100883200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:100871800-100877600	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr8:100871800-100887600	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:100872000-100877800	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr8:100872000-100883800	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr8:100872000-100898200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr8:100872200-100878000	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr8:100872200-100884800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr8:100872400-100879000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr8:100872400-100883400	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr8:100872400-100883600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr8:100872400-100884400	Weak transcription	Brain Angular Gyrus	brain
24	chr8:100872400-100884400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr8:100872600-100877000	Weak transcription	Right Atrium	heart
26	chr8:100872600-100882800	Weak transcription	K562	blood
27	chr8:100872600-100883200	Weak transcription	Brain Substantia Nigra	brain
28	chr8:100872600-100883600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:100872600-100885000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr8:100872800-100878600	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr8:100872800-100883600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr8:100872800-100883800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr8:100872800-100883800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr8:100872800-100885200	Weak transcription	Hela-S3	cervix
35	chr8:100872800-100903800	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr8:100873000-100878800	Strong transcription	Fetal Muscle Leg	muscle
37	chr8:100873000-100885800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:100873200-100881400	Weak transcription	Brain Anterior Caudate	brain
39	chr8:100873200-100882600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr8:100873200-100882800	Weak transcription	Brain Hippocampus Middle	brain
41	chr8:100873200-100883000	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr8:100873200-100883200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr8:100873200-100883400	Weak transcription	HMEC	breast
44	chr8:100873200-100885400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:100873200-100885400	Weak transcription	NHEK	skin
46	chr8:100873200-100886800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr8:100873400-100877200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr8:100873400-100878200	Strong transcription	Fetal Intestine Large	intestine
49	chr8:100873400-100881200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr8:100873400-100883400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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