Variant report

Variant	rs143263932
Chromosome Location	chr13:110496257-110496258
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv976222	chr13:110495093-110499364	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110489600-110497200	Weak transcription	Stomach Mucosa	stomach
2	chr13:110492800-110496600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr13:110493000-110496600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr13:110493000-110497800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr13:110493200-110498600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr13:110493200-110499200	Weak transcription	Right Atrium	heart
7	chr13:110493600-110496600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr13:110493600-110496600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr13:110493600-110496600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr13:110493600-110496600	Weak transcription	Osteobl	bone
11	chr13:110493800-110496800	Weak transcription	HMEC	breast
12	chr13:110493800-110497000	Weak transcription	NH-A	brain
13	chr13:110494000-110497000	Weak transcription	HSMMtube	muscle
14	chr13:110494800-110496600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr13:110494800-110496600	Weak transcription	HSMM	muscle
16	chr13:110495800-110497200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr13:110496000-110496600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
18	chr13:110496000-110496600	Flanking Active TSS	Stomach Smooth Muscle	stomach
19	chr13:110496000-110497600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr13:110496200-110496400	Enhancers	Aorta	Aorta
21	chr13:110496200-110496400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
22	chr13:110496200-110496600	Enhancers	Colon Smooth Muscle	Colon
23	chr13:110496200-110497600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr13:110496200-110497600	Enhancers	Rectal Smooth Muscle	rectum

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