Variant report

Variant	rs7836549
Chromosome Location	chr8:117697574-117697575
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:117697505..117699043-chr8:117703582..117706384,2	K562	blood:
2	chr8:117696331..117699023-chr8:117777229..117780131,3	K562	blood:
3	chr8:117686959..117689799-chr8:117696195..117697939,2	MCF-7	breast:
4	chr8:117695254..117697926-chr8:117699947..117701822,2	K562	blood:
5	chr8:117694279..117697121-chr8:117697195..117699219,2	K562	blood:

Variant related genes	Relation type
ENSG00000147679	Chromatin interaction
ENSG00000147677	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10085939	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10086419	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10088177	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10093551	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10096134	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10105610	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10112279	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10112604	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10283129	0.88[YRI][hapmap]
rs10505282	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10505286	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs10505287	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10808484	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11781970	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12547058	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1317271	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13258529	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs13262725	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13277714	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13277958	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1347626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1436765	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1436766	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1529945	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2118108	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3088140	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34519652	0.83[EUR][1000 genomes]
rs35338453	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35905748	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4256624	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4278180	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4289846	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4289847	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4335152	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4335153	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4422805	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4472547	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4601347	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4623456	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4629900	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4645587	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4876679	0.93[YRI][hapmap]
rs55951040	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6469656	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6469657	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6980504	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6983032	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6988841	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6996020	0.85[YRI][hapmap]
rs7007250	0.83[EUR][1000 genomes]
rs7013617	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7464414	0.83[EUR][1000 genomes]
rs7820778	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7830860	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7831811	0.86[YRI][hapmap]
rs7833054	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7833618	0.81[YRI][hapmap]
rs7843852	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530386	chr8:117509968-118391406	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:117654600-117715200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:117659000-117698000	Weak transcription	Hela-S3	cervix
3	chr8:117666000-117699000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr8:117667000-117699200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr8:117668200-117707000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr8:117670200-117707000	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr8:117671000-117717600	Weak transcription	HepG2	liver
8	chr8:117674800-117706800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr8:117675800-117697600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:117677400-117699200	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr8:117678200-117697600	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr8:117678200-117700600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr8:117678200-117705600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr8:117679000-117703200	Weak transcription	Brain Hippocampus Middle	brain
15	chr8:117681200-117698000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr8:117682800-117698600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr8:117682800-117703400	Weak transcription	Primary T cells from cord blood	blood
18	chr8:117682800-117707400	Weak transcription	Right Atrium	heart
19	chr8:117684000-117698600	Weak transcription	Fetal Stomach	stomach
20	chr8:117684000-117698800	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr8:117684200-117700400	Weak transcription	K562	blood
22	chr8:117685200-117698800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:117685400-117707200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr8:117686200-117703200	Weak transcription	GM12878-XiMat	blood
25	chr8:117690000-117697600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr8:117690000-117698800	Weak transcription	Fetal Kidney	kidney
27	chr8:117690000-117707000	Weak transcription	Primary B cells from cord blood	blood
28	chr8:117690400-117697800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:117693400-117700000	Weak transcription	Fetal Intestine Small	intestine
30	chr8:117694600-117703200	Weak transcription	Brain Substantia Nigra	brain
31	chr8:117695400-117697600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr8:117695400-117699400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:117695600-117704400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:117695600-117707600	Weak transcription	Dnd41	blood
35	chr8:117695800-117698800	Weak transcription	Left Ventricle	heart
36	chr8:117696200-117697600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:117696200-117697600	Enhancers	Colon Smooth Muscle	Colon
38	chr8:117696400-117698800	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr8:117696600-117697800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr8:117696600-117698200	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr8:117696800-117698400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr8:117696800-117700600	Enhancers	HUVEC	blood vessel
43	chr8:117697000-117698200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr8:117697000-117701000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr8:117697000-117704800	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr8:117697200-117697600	Enhancers	Rectal Smooth Muscle	rectum
47	chr8:117697200-117701400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr8:117697200-117701400	Enhancers	Fetal Heart	heart
49	chr8:117697200-117701600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:117697200-117702400	Weak transcription	Brain Anterior Caudate	brain

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