Variant report

Variant	rs535337863
Chromosome Location	chr10:25336235-25336236
allele	C/T
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	nsv550224	chr10:25335854-25385858	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25335400-25337000	Enhancers	K562	blood
2	chr10:25335600-25336400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr10:25335600-25336400	Enhancers	Fetal Brain Female	brain
4	chr10:25335600-25337200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr10:25335600-25338000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr10:25336000-25336800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr10:25336000-25337800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:25336000-25337800	Enhancers	HMEC	breast
9	chr10:25336000-25338000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:25336000-25338000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr10:25336200-25336600	Enhancers	Brain Angular Gyrus	brain
12	chr10:25336200-25337200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:25336200-25337400	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr10:25336200-25337600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr10:25336200-25337600	Enhancers	Osteobl	bone
16	chr10:25336200-25337800	Enhancers	NHEK	skin
17	chr10:25336200-25338200	Enhancers	Fetal Intestine Small	intestine

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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