Variant report

Variant	rs151331207
Chromosome Location	chr5:98356467-98356468
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:98263973..98268060-chr5:98355511..98358159,6	K562	blood:
2	chr5:98264797..98266835-chr5:98354593..98357011,2	K562	blood:
3	chr5:98355578..98358107-chr5:98362158..98365732,4	K562	blood:
4	chr5:98262156..98264317-chr5:98355438..98358771,4	K562	blood:

Variant related genes	Relation type
ENSG00000153922	Chromatin interaction
ENSG00000248489	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1826071	chr5:98312447-98358852	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv1827754	chr5:98312447-98358852	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv1837772	chr5:98312447-98358852	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv1838335	chr5:98312447-98358852	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv1845131	chr5:98312447-98358852	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv599093	chr5:98344571-98356733	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv599099	chr5:98345182-98356733	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv599100	chr5:98345182-98357415	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv1794778	chr5:98345182-98358852	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv1825119	chr5:98345182-98358852	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv599103	chr5:98345287-98356733	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv599107	chr5:98345400-98356733	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	nsv599113	chr5:98345632-98357415	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv1024391	chr5:98355665-98653657	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:98353600-98358000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:98353600-98361600	Weak transcription	Small Intestine	intestine
3	chr5:98354600-98357000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:98354600-98357000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:98354800-98356800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:98354800-98357000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr5:98355000-98356600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:98355000-98356600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr5:98355000-98356600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr5:98355000-98356600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr5:98355000-98356600	Enhancers	Hela-S3	cervix
12	chr5:98355000-98356800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:98355000-98356800	Enhancers	NH-A	brain
14	chr5:98355000-98356800	Enhancers	Osteobl	bone
15	chr5:98355000-98358200	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr5:98355000-98358400	Enhancers	Fetal Intestine Small	intestine
17	chr5:98355000-98358600	Enhancers	Fetal Intestine Large	intestine
18	chr5:98355400-98356600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr5:98355400-98357000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr5:98355400-98357000	Enhancers	Liver	Liver
21	chr5:98355400-98357400	Enhancers	Duodenum Mucosa	Duodenum
22	chr5:98355600-98356600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr5:98355600-98356600	Enhancers	HMEC	breast
24	chr5:98355600-98356800	Enhancers	Adipose Nuclei	Adipose
25	chr5:98355600-98356800	Enhancers	A549	lung
26	chr5:98355600-98358400	Enhancers	HepG2	liver
27	chr5:98355800-98356600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr5:98356000-98356600	Enhancers	NHDF-Ad	bronchial
29	chr5:98356000-98356800	Enhancers	HUVEC	blood vessel
30	chr5:98356000-98360600	Weak transcription	Colonic Mucosa	Colon
31	chr5:98356400-98356600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:98356400-98356800	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr5:98356400-98357200	Weak transcription	K562	blood
34	chr5:98356400-98357600	Weak transcription	Stomach Mucosa	stomach
35	chr5:98356400-98360400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr5:98356400-98360400	Weak transcription	GM12878-XiMat	blood
37	chr5:98356400-98361000	Weak transcription	Primary hematopoietic stem cells	blood
38	chr5:98356400-98361000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr5:98356400-98361000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:98356400-98361200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr5:98356400-98361200	Weak transcription	Fetal Stomach	stomach
42	chr5:98356400-98361600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr5:98356400-98361800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr5:98356400-98362400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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