Variant report

Variant	rs187367798
Chromosome Location	chr18:21087599-21087600
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:21086304..21090723-chr18:21165251..21167811,3	MCF-7	breast:
2	chr18:21087453..21090115-chr18:21090407..21093336,2	K562	blood:
3	chr18:21085040..21087819-chr18:21093898..21095823,3	K562	blood:
4	chr18:21069860..21072845-chr18:21087442..21089304,2	K562	blood:
5	chr18:21086417..21089145-chr18:21091032..21093812,2	MCF-7	breast:
6	chr18:21082338..21086201-chr18:21086505..21089611,5	MCF-7	breast:
7	chr18:21085828..21087775-chr18:21166475..21168168,2	K562	blood:

Variant related genes	Relation type
ENSG00000141452	Chromatin interaction
ENSG00000141458	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34149	chr18:20858139-21221891	Bivalent Enhancer Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv431973	chr18:20861916-21118980	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv431974	chr18:20861916-21119291	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv909458	chr18:21003061-21171145	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv995053	chr18:21057147-21333688	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	nsv576572	chr18:21087531-21171145	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:21084200-21088000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr18:21084400-21088000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr18:21084400-21097400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr18:21084400-21098600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr18:21084400-21099800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr18:21084400-21102000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr18:21084600-21087800	Weak transcription	Right Ventricle	heart
8	chr18:21084600-21088000	Weak transcription	Fetal Muscle Trunk	muscle
9	chr18:21084600-21100400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr18:21084800-21087600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr18:21084800-21087600	Enhancers	Brain Substantia Nigra	brain
12	chr18:21084800-21088000	Weak transcription	HSMMtube	muscle
13	chr18:21084800-21088200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr18:21084800-21088400	Genic enhancers	Primary B cells from peripheral blood	blood
15	chr18:21084800-21090600	Weak transcription	Fetal Brain Male	brain
16	chr18:21085000-21087600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr18:21085000-21087600	Weak transcription	NHLF	lung
18	chr18:21085000-21088000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr18:21085000-21088000	Weak transcription	Fetal Lung	lung
20	chr18:21085000-21088000	Weak transcription	A549	lung
21	chr18:21085000-21088600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr18:21085000-21090200	Weak transcription	HMEC	breast
23	chr18:21085000-21090400	Weak transcription	Fetal Kidney	kidney
24	chr18:21085000-21099600	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr18:21085200-21087600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr18:21085200-21091400	Strong transcription	Fetal Stomach	stomach
27	chr18:21085200-21092600	Strong transcription	Fetal Intestine Small	intestine
28	chr18:21085200-21098800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr18:21085400-21090400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr18:21085400-21091600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr18:21085400-21118800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr18:21085600-21087600	Weak transcription	HepG2	liver
33	chr18:21085600-21088000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr18:21085600-21088000	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr18:21085600-21088400	Weak transcription	Colonic Mucosa	Colon
36	chr18:21085600-21088800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr18:21085600-21090400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr18:21085600-21092200	Strong transcription	Fetal Thymus	thymus
39	chr18:21085600-21097400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr18:21085600-21101400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr18:21085600-21109600	Weak transcription	Fetal Heart	heart
42	chr18:21085600-21112200	Weak transcription	Right Atrium	heart
43	chr18:21085600-21119000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr18:21085800-21087800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr18:21085800-21087800	Weak transcription	Thymus	Thymus
46	chr18:21085800-21088000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr18:21085800-21088000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr18:21085800-21088000	Weak transcription	Adipose Nuclei	Adipose
49	chr18:21085800-21088000	Weak transcription	Aorta	Aorta
50	chr18:21085800-21088000	Weak transcription	Gastric	stomach

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