Variant report

Variant	rs117637131
Chromosome Location	chr18:13232615-13232616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:13229701..13231556-chr18:13232508..13235407,3	MCF-7	breast:
2	chr18:13226398..13229560-chr18:13232125..13236070,6	MCF-7	breast:
3	chr18:13217269..13219226-chr18:13231988..13233808,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000168675	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv833591	chr18:13093777-13253748	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv909408	chr18:13122618-13308950	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv909409	chr18:13151544-13240284	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv909410	chr18:13151544-13308950	Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	esv2182710	chr18:13232298-13232753	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:13223400-13235400	Weak transcription	Fetal Kidney	kidney
2	chr18:13223600-13235600	Weak transcription	Fetal Intestine Small	intestine
3	chr18:13223600-13241400	Weak transcription	Aorta	Aorta
4	chr18:13223800-13234200	Weak transcription	Liver	Liver
5	chr18:13223800-13259800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr18:13224000-13234800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr18:13224000-13235400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr18:13224000-13259800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr18:13224200-13233400	Weak transcription	HepG2	liver
10	chr18:13224400-13234000	Weak transcription	Pancreas	Pancrea
11	chr18:13224400-13234600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr18:13224400-13235400	Weak transcription	Colon Smooth Muscle	Colon
13	chr18:13224400-13235600	Weak transcription	Duodenum Mucosa	Duodenum
14	chr18:13224400-13242600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr18:13224400-13245400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr18:13224400-13259800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr18:13228200-13232800	Weak transcription	Esophagus	oesophagus
18	chr18:13229400-13243000	Weak transcription	Dnd41	blood
19	chr18:13229800-13233000	Weak transcription	Primary T cells from cord blood	blood
20	chr18:13230600-13240800	Enhancers	Fetal Brain Male	brain
21	chr18:13231000-13233000	Strong transcription	Fetal Thymus	thymus
22	chr18:13231200-13233400	Enhancers	Fetal Muscle Leg	muscle
23	chr18:13231400-13234200	Enhancers	Fetal Heart	heart
24	chr18:13231800-13233400	Enhancers	Brain Germinal Matrix	brain
25	chr18:13231800-13233600	Enhancers	Fetal Lung	lung
26	chr18:13231800-13234600	Enhancers	Left Ventricle	heart
27	chr18:13231800-13234800	Enhancers	Right Ventricle	heart
28	chr18:13232000-13232800	Enhancers	Psoas Muscle	Psoas
29	chr18:13232000-13233000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr18:13232000-13233200	Enhancers	Right Atrium	heart
31	chr18:13232000-13233600	Bivalent Enhancer	Fetal Stomach	stomach
32	chr18:13232000-13233600	Enhancers	Gastric	stomach
33	chr18:13232000-13234800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr18:13232200-13233000	Enhancers	Adipose Nuclei	Adipose
35	chr18:13232200-13233000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
36	chr18:13232200-13233000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr18:13232200-13233000	Enhancers	Spleen	Spleen
38	chr18:13232200-13233200	Flanking Active TSS	Brain Cingulate Gyrus	brain
39	chr18:13232400-13233000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr18:13232400-13233000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr18:13232400-13233000	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr18:13232400-13233000	Enhancers	Colonic Mucosa	Colon
43	chr18:13232400-13233000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr18:13232400-13233200	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr18:13232400-13233600	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr18:13232600-13232800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
47	chr18:13232600-13232800	Enhancers	Fetal Brain Female	brain
48	chr18:13232600-13233000	Active TSS	Brain Angular Gyrus	brain
49	chr18:13232600-13233000	Active TSS	Brain Substantia Nigra	brain
50	chr18:13232600-13233200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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