Variant report

Variant	rs67539049
Chromosome Location	chr8:11307311-11307312
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:11299743..11301452-chr8:11307305..11309157,2	MCF-7	breast:
2	chr8:11306300..11308613-chr8:11308996..11313515,5	K562	blood:
3	chr8:11306364..11309144-chr8:11311400..11314118,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000154319	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12115021	0.83[EUR][1000 genomes]
rs2001462	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3021512	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3021517	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3021518	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55764254	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56003968	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56138616	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56235592	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56286613	0.92[EUR][1000 genomes]
rs56388647	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58319820	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs58387061	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs60320871	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs66934548	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs67350204	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs67526040	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs67684445	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs67909842	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67932868	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs68063127	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73207493	0.90[EUR][1000 genomes]
rs73207496	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73207500	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73209223	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73209241	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73209243	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73209249	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73209250	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73546310	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73546312	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7832089	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7835996	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv1022525	chr8:11066191-11309356	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv539474	chr8:11066191-11309356	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv522860	chr8:11253879-11330364	Bivalent/Poised TSS Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv890357	chr8:11286146-11330364	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1030756	chr8:11292073-11332782	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1022074	chr8:11292256-11394526	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11280600-11308800	Weak transcription	Primary B cells from cord blood	blood
2	chr8:11287800-11313600	Weak transcription	Right Atrium	heart
3	chr8:11292400-11313000	Weak transcription	Pancreas	Pancrea
4	chr8:11296200-11319200	Enhancers	Fetal Thymus	thymus
5	chr8:11298800-11308600	Weak transcription	Primary B cells from peripheral blood	blood
6	chr8:11303600-11323200	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr8:11304600-11308200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr8:11304600-11308400	Weak transcription	Thymus	Thymus
9	chr8:11305000-11307400	Enhancers	Brain Anterior Caudate	brain
10	chr8:11305200-11307800	Enhancers	Placenta	Placenta
11	chr8:11305800-11307600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:11305800-11308200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:11305800-11308200	Enhancers	Fetal Brain Female	brain
14	chr8:11305800-11308200	Enhancers	Osteobl	bone
15	chr8:11305800-11310600	Enhancers	Brain Substantia Nigra	brain
16	chr8:11305800-11312200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:11306000-11307400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr8:11306000-11307800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr8:11306000-11308000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:11306000-11308600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr8:11306000-11310400	Enhancers	Brain Angular Gyrus	brain
22	chr8:11306000-11310400	Enhancers	Brain Cingulate Gyrus	brain
23	chr8:11306000-11310400	Enhancers	Brain Hippocampus Middle	brain
24	chr8:11306200-11307400	Weak transcription	Fetal Kidney	kidney
25	chr8:11306200-11307800	Enhancers	Fetal Brain Male	brain
26	chr8:11306400-11307400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:11306400-11311800	Weak transcription	Gastric	stomach
28	chr8:11306400-11312200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr8:11306600-11307400	Enhancers	Esophagus	oesophagus
30	chr8:11306600-11311400	Weak transcription	A549	lung
31	chr8:11306800-11308600	Weak transcription	GM12878-XiMat	blood
32	chr8:11306800-11308800	Weak transcription	Spleen	Spleen
33	chr8:11306800-11310400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr8:11307000-11307400	Weak transcription	Right Ventricle	heart
35	chr8:11307000-11307600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr8:11307000-11307800	Enhancers	NHEK	skin
37	chr8:11307000-11308200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:11307000-11308600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:11307000-11311400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:11307000-11311400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr8:11307200-11307400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:11307200-11307400	Enhancers	Primary hematopoietic stem cells	blood
43	chr8:11307200-11308000	Weak transcription	Brain Germinal Matrix	brain
44	chr8:11307200-11314000	Weak transcription	Fetal Heart	heart
45	chr8:11307200-11322000	Weak transcription	HSMMtube	muscle

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