Variant report

Variant	rs74131781
Chromosome Location	chr10:52920670-52920671
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036645	chr10:52804961-53159076	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	esv2587039	chr10:52920340-52921906	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv2185716	chr10:52920669-52920671	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52895200-52924000	Weak transcription	Fetal Stomach	stomach
2	chr10:52906000-52931200	Weak transcription	Fetal Muscle Leg	muscle
3	chr10:52908000-52929600	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr10:52908400-52929600	Weak transcription	Aorta	Aorta
5	chr10:52910000-52931000	Weak transcription	Fetal Lung	lung
6	chr10:52910600-52942400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr10:52913000-52922000	Weak transcription	Right Ventricle	heart
8	chr10:52913200-52921800	Weak transcription	Colon Smooth Muscle	Colon
9	chr10:52917000-52921400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr10:52917200-52921600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr10:52917200-52921600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr10:52917200-52921600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:52917200-52921600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr10:52917200-52921800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr10:52917400-52929000	Weak transcription	NHDF-Ad	bronchial
16	chr10:52919400-52921800	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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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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