Variant report

Variant	rs73276542
Chromosome Location	chr10:44289892-44289893
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44277800-44295000	Weak transcription	Spleen	Spleen
2	chr10:44286000-44302600	Weak transcription	Aorta	Aorta
3	chr10:44286800-44292400	Weak transcription	Ovary	ovary
4	chr10:44287600-44290000	Enhancers	Fetal Lung	lung
5	chr10:44288600-44290200	Enhancers	Fetal Muscle Leg	muscle
6	chr10:44289000-44290000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr10:44289000-44290000	Enhancers	NHDF-Ad	bronchial
8	chr10:44289000-44290200	Enhancers	Adipose Nuclei	Adipose
9	chr10:44289000-44290800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:44289000-44290800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr10:44289200-44290000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr10:44289400-44290000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr10:44289400-44290000	Enhancers	Fetal Stomach	stomach
14	chr10:44289600-44290000	Enhancers	Right Atrium	heart
15	chr10:44289600-44290000	Enhancers	Osteobl	bone
16	chr10:44289600-44290200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr10:44289800-44290000	Enhancers	Liver	Liver
18	chr10:44289800-44290200	Enhancers	Fetal Muscle Trunk	muscle

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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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