Variant report

Variant	rs3805714
Chromosome Location	chr5:41156923-41156924
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41139800-41182000	Weak transcription	Left Ventricle	heart
2	chr5:41151000-41181400	Weak transcription	Fetal Intestine Small	intestine
3	chr5:41153200-41169000	Weak transcription	Pancreas	Pancrea
4	chr5:41155000-41159200	Weak transcription	Adipose Nuclei	Adipose
5	chr5:41155200-41157400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:41155200-41161600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr5:41156400-41157000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:41156400-41157800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr5:41156400-41160200	Genic enhancers	Liver	Liver
10	chr5:41156600-41157800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:41156600-41169000	Weak transcription	Fetal Intestine Large	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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