Variant report

Variant	rs2387331
Chromosome Location	chr8:102990347-102990348
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	chr8:102989164..102991049-chr8:102992314..102994744,2	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10089091	0.92[CEU][hapmap]
rs10090732	1.00[CEU][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10091084	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10102923	0.90[CEU][hapmap];0.84[EUR][1000 genomes]
rs10105502	1.00[CEU][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10505017	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs1269711	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs1269712	0.86[EUR][1000 genomes]
rs16868893	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs1992330	1.00[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs2023268	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2023269	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28379664	0.81[EUR][1000 genomes]
rs28680363	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34417909	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4734049	0.92[CEU][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4734050	0.92[CEU][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4734052	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs4734607	1.00[CEU][hapmap];1.00[JPT][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4734609	0.92[CEU][hapmap]
rs55837041	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs59321812	0.84[EUR][1000 genomes]
rs60389438	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6468809	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs72679088	0.85[EUR][1000 genomes]
rs7814225	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7814951	0.91[CEU][hapmap]
rs7818772	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7837198	1.00[CEU][hapmap]
rs9297317	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9656850	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs984928	1.00[CEU][hapmap];1.00[JPT][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9886578	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018653	chr8:102818271-103009082	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv539700	chr8:102818271-103009082	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv831411	chr8:102937991-103108140	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102976000-102992000	Weak transcription	Right Ventricle	heart
2	chr8:102981000-102992000	Weak transcription	Esophagus	oesophagus
3	chr8:102983400-102991400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:102983600-102991200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr8:102983600-102992000	Weak transcription	Left Ventricle	heart
6	chr8:102986400-102990400	Weak transcription	Fetal Heart	heart
7	chr8:102987200-102991000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr8:102987400-102990800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr8:102987800-102992000	Weak transcription	Lung	lung
10	chr8:102988200-102991000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr8:102988200-102991200	Weak transcription	K562	blood
12	chr8:102988400-102991200	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr8:102988600-102991400	Weak transcription	Spleen	Spleen
14	chr8:102988600-102992600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:102989000-102990800	Enhancers	GM12878-XiMat	blood
16	chr8:102989000-102993400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr8:102989600-102991000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:102989600-102993200	Enhancers	Ovary	ovary
19	chr8:102989800-102990400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:102989800-102990400	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr8:102989800-102990400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr8:102989800-102990400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:102989800-102990600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr8:102989800-102990600	Enhancers	Stomach Smooth Muscle	stomach
25	chr8:102989800-102992400	Enhancers	Fetal Brain Male	brain
26	chr8:102989800-102992600	Enhancers	Aorta	Aorta
27	chr8:102989800-102994800	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr8:102990000-102990800	Weak transcription	Fetal Muscle Leg	muscle
29	chr8:102990000-102990800	Weak transcription	Psoas Muscle	Psoas
30	chr8:102990000-102991200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr8:102990000-102991400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr8:102990000-102992200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:102990200-102990400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:102990200-102991400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr8:102990200-102991400	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr8:102990200-102992200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:102990200-102992400	Weak transcription	HMEC	breast
38	chr8:102990200-102992400	Weak transcription	NHEK	skin
39	chr8:102990200-102993000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr8:102990200-102996000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links