Variant report

Variant	rs1757235
Chromosome Location	chr10:18527039-18527040
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18515800-18532000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:18523000-18549400	Weak transcription	Pancreas	Pancrea
3	chr10:18523200-18529600	Weak transcription	Esophagus	oesophagus
4	chr10:18523200-18529600	Weak transcription	Left Ventricle	heart
5	chr10:18523200-18536000	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr10:18523400-18529200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr10:18524400-18527200	Enhancers	Colon Smooth Muscle	Colon
8	chr10:18525600-18527400	Enhancers	Ovary	ovary
9	chr10:18526000-18532200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr10:18526200-18527400	Weak transcription	Fetal Heart	heart
11	chr10:18526200-18528000	Enhancers	Fetal Lung	lung
12	chr10:18526200-18536000	Weak transcription	Right Atrium	heart
13	chr10:18526600-18528400	Enhancers	Aorta	Aorta
14	chr10:18526800-18527200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr10:18526800-18527600	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr10:18527000-18527600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr10:18527000-18548800	Weak transcription	Stomach Smooth Muscle	stomach

Quick Search:

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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