Variant report

Variant	rs148084455
Chromosome Location	chr8:48265869-48265870
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:48263378..48268282-chr8:48268711..48274538,7	MCF-7	breast:
2	chr8:48264421..48266947-chr8:48288790..48290307,2	MCF-7	breast:
3	chr8:48264373..48267024-chr8:48650520..48652799,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164808	Chromatin interaction
ENSG00000221869	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015347	chr8:47698082-48318579	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
2	nsv539593	chr8:47698082-48318579	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
3	esv3693377	chr8:47824261-48582964	Genic enhancers Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	nsv491863	chr8:48053825-48586176	Strong transcription Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	esv2758155	chr8:48188989-48321308	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv2759610	chr8:48188989-48321308	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv1817304	chr8:48205314-48321308	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1034660	chr8:48265109-48411279	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48209400-48266000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr8:48230400-48267400	Weak transcription	Spleen	Spleen
3	chr8:48238800-48274600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:48247800-48276400	Weak transcription	Colonic Mucosa	Colon
5	chr8:48248800-48309600	Weak transcription	Thymus	Thymus
6	chr8:48249200-48282000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr8:48249800-48266000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr8:48249800-48267200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr8:48249800-48277400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr8:48249800-48277800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr8:48253400-48267200	Weak transcription	Lung	lung
12	chr8:48253400-48274400	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr8:48253600-48273800	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr8:48254600-48268400	Weak transcription	Gastric	stomach
15	chr8:48256200-48274200	Weak transcription	Esophagus	oesophagus
16	chr8:48256400-48272200	Weak transcription	GM12878-XiMat	blood
17	chr8:48256400-48274200	Weak transcription	Primary T cells from cord blood	blood
18	chr8:48256400-48276200	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr8:48256400-48276800	Weak transcription	Dnd41	blood
20	chr8:48256400-48281000	Weak transcription	Primary hematopoietic stem cells	blood
21	chr8:48256600-48267400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr8:48256600-48273000	Weak transcription	Primary B cells from peripheral blood	blood
23	chr8:48262400-48309600	Weak transcription	Fetal Stomach	stomach
24	chr8:48263200-48297200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr8:48264400-48267000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr8:48264400-48276000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr8:48264600-48266200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:48264600-48266200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr8:48264600-48266200	Enhancers	Pancreas	Pancrea
30	chr8:48264800-48266400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:48264800-48266400	Enhancers	HMEC	breast
32	chr8:48264800-48266600	Enhancers	NHEK	skin
33	chr8:48264800-48271000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr8:48265000-48266200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr8:48265000-48266600	Enhancers	NHLF	lung
36	chr8:48265000-48266800	Enhancers	HSMMtube	muscle
37	chr8:48265000-48267000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr8:48265000-48267000	Enhancers	HSMM	muscle
39	chr8:48265000-48267000	Enhancers	NH-A	brain
40	chr8:48265000-48267200	Enhancers	Liver	Liver
41	chr8:48265000-48268200	Enhancers	Stomach Mucosa	stomach
42	chr8:48265000-48273200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr8:48265200-48266200	Enhancers	Placenta	Placenta
44	chr8:48265200-48266200	Enhancers	Left Ventricle	heart
45	chr8:48265200-48266400	Weak transcription	Primary B cells from cord blood	blood
46	chr8:48265400-48266200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr8:48265400-48266800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:48265400-48267200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr8:48265600-48266600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr8:48265600-48266600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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