Variant report

Variant	rs17155179
Chromosome Location	chr8:8937822-8937823
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:8935014..8937829-chr8:9004036..9006793,2	MCF-7	breast:
2	chr8:8935137..8938110-chr8:8938203..8940506,3	MCF-7	breast:
3	chr8:8935360..8937966-chr8:9011141..9013964,2	MCF-7	breast:
4	chr8:8932433..8935466-chr8:8936336..8937882,3	K562	blood:

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11774329	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17155176	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs17155181	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6601286	1.00[CEU][hapmap];0.82[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6987277	1.00[CEU][hapmap];0.90[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7818455	1.00[CEU][hapmap];0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7825188	0.94[CEU][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890331	chr8:8093240-8971100	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats 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 miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv917117	chr8:8621658-9313799	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv1022468	chr8:8857853-9209167	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv539460	chr8:8857853-9209167	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv817373	chr8:8857854-9361049	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8924000-8939600	Weak transcription	Right Ventricle	heart
2	chr8:8929600-8940000	Weak transcription	Aorta	Aorta
3	chr8:8930200-8940400	Enhancers	Fetal Intestine Large	intestine
4	chr8:8931600-8938000	Enhancers	Placenta	Placenta
5	chr8:8931800-8940800	Enhancers	Fetal Intestine Small	intestine
6	chr8:8932600-8939600	Weak transcription	Ovary	ovary
7	chr8:8932600-8951800	Weak transcription	Pancreas	Pancrea
8	chr8:8932800-8939200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:8932800-8945600	Weak transcription	Thymus	Thymus
10	chr8:8933000-8939400	Enhancers	K562	blood
11	chr8:8933200-8938000	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr8:8933200-8938000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr8:8933200-8938200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr8:8933200-8938200	Weak transcription	Colon Smooth Muscle	Colon
15	chr8:8933200-8938800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr8:8933200-8939400	Weak transcription	Fetal Lung	lung
17	chr8:8933200-8939600	Weak transcription	Rectal Smooth Muscle	rectum
18	chr8:8933400-8938000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr8:8933600-8939200	Weak transcription	Primary hematopoietic stem cells	blood
20	chr8:8934200-8940000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr8:8935000-8939600	Weak transcription	NHLF	lung
22	chr8:8935200-8939400	Weak transcription	HSMM	muscle
23	chr8:8935200-8939600	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr8:8935400-8938000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:8935400-8938200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr8:8935400-8939000	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr8:8935400-8939000	Weak transcription	Osteobl	bone
28	chr8:8935400-8939400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:8935400-8939400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr8:8935400-8939400	Weak transcription	NH-A	brain
31	chr8:8935400-8939600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr8:8935400-8939600	Weak transcription	HSMMtube	muscle
33	chr8:8935400-8959600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr8:8935600-8939400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr8:8935600-8939600	Weak transcription	Psoas Muscle	Psoas
36	chr8:8935600-8939600	Weak transcription	Right Atrium	heart
37	chr8:8935800-8940000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr8:8936000-8940400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr8:8936200-8938200	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr8:8936200-8938400	Enhancers	Colonic Mucosa	Colon
41	chr8:8936200-8940000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr8:8936200-8940400	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr8:8936400-8940400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr8:8936600-8938000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:8936600-8939000	Weak transcription	HMEC	breast
46	chr8:8936600-8939200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:8936600-8939600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:8936800-8938000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:8936800-8938000	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr8:8936800-8938800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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