Variant report

Variant	rs553132154
Chromosome Location	chr10:116311643-116311644
allele	-/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:116308927..116312101-chr10:116579635..116582119,3	MCF-7	breast:
2	chr10:116310252..116311787-chr10:116463124..116463956,6	MCF-7	breast:
3	chr10:116309046..116312030-chr10:116580790..116583146,2	MCF-7	breast:
4	chr10:116310031..116311847-chr10:116382346..116385171,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000151553	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1037308	chr10:116141946-116519765	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv540780	chr10:116141946-116519765	Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	esv3336522	chr10:116310912-116312672	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv949138	chr10:116311531-116874477	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116305000-116317600	Weak transcription	Fetal Muscle Trunk	muscle
2	chr10:116305200-116316000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:116305200-116318200	Weak transcription	Fetal Intestine Large	intestine
4	chr10:116307600-116313400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr10:116307600-116316000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr10:116307800-116317600	Weak transcription	Fetal Intestine Small	intestine
7	chr10:116308600-116312600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr10:116308600-116313200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr10:116308600-116315800	Weak transcription	HepG2	liver
10	chr10:116308800-116313200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr10:116309000-116316400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr10:116310400-116311800	Enhancers	Small Intestine	intestine
13	chr10:116310600-116312000	Enhancers	Left Ventricle	heart
14	chr10:116310600-116312000	Enhancers	Ovary	ovary
15	chr10:116310600-116313000	Enhancers	Fetal Muscle Leg	muscle
16	chr10:116310800-116311800	Flanking Active TSS	Fetal Lung	lung
17	chr10:116310800-116312000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr10:116310800-116312000	Enhancers	Fetal Stomach	stomach
19	chr10:116310800-116312000	Enhancers	Fetal Thymus	thymus
20	chr10:116310800-116312000	Enhancers	Pancreas	Pancrea
21	chr10:116310800-116312000	Enhancers	Right Ventricle	heart
22	chr10:116310800-116312400	Enhancers	Psoas Muscle	Psoas
23	chr10:116310800-116312400	Enhancers	Stomach Mucosa	stomach
24	chr10:116310800-116317400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr10:116311000-116311800	Enhancers	Brain Angular Gyrus	brain
26	chr10:116311000-116311800	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr10:116311000-116312000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr10:116311000-116312000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr10:116311000-116312000	Enhancers	Brain Substantia Nigra	brain
30	chr10:116311000-116312000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr10:116311000-116312200	Enhancers	Brain Cingulate Gyrus	brain
32	chr10:116311000-116312200	Enhancers	Brain Germinal Matrix	brain
33	chr10:116311000-116312400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:116311000-116312600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr10:116311000-116314000	Weak transcription	Aorta	Aorta
36	chr10:116311000-116317400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr10:116311000-116331400	Weak transcription	Fetal Brain Male	brain
38	chr10:116311200-116311800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr10:116311200-116311800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr10:116311200-116312200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr10:116311200-116312200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr10:116311400-116311800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr10:116311400-116311800	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr10:116311400-116312000	Enhancers	Esophagus	oesophagus
45	chr10:116311400-116312000	Enhancers	Lung	lung
46	chr10:116311400-116312000	Flanking Active TSS	Right Atrium	heart
47	chr10:116311400-116312200	Enhancers	Brain Hippocampus Middle	brain
48	chr10:116311400-116312200	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr10:116311400-116312200	Enhancers	Rectal Smooth Muscle	rectum
50	chr10:116311600-116311800	Enhancers	Colon Smooth Muscle	Colon

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