Variant report

Variant	rs11337812
Chromosome Location	chr10:18704397-18704398
allele	-/A
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	nsv550042	chr10:18683267-18994583	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1053675	chr10:18703895-18722912	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2041200	chr10:18704397-18704398	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18690000-18705600	Weak transcription	Aorta	Aorta
2	chr10:18690200-18713000	Weak transcription	Ovary	ovary
3	chr10:18692000-18712600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr10:18692600-18707600	Weak transcription	Brain Angular Gyrus	brain
5	chr10:18701000-18705800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr10:18702800-18707600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr10:18703000-18705400	Weak transcription	Right Ventricle	heart
8	chr10:18703200-18711200	Weak transcription	Stomach Smooth Muscle	stomach
9	chr10:18703600-18707000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr10:18703600-18707000	Weak transcription	Left Ventricle	heart
11	chr10:18703600-18732000	Weak transcription	Pancreas	Pancrea
12	chr10:18703800-18704800	Enhancers	Fetal Heart	heart

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

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