Variant report

Variant rs2821086
Chromosome Location chr1:47679079-47679080
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:47674400-47690600 Weak transcription Gastric stomach
2 chr1:47675400-47680000 Enhancers HUVEC blood vessel
3 chr1:47675800-47680600 Enhancers Primary hematopoietic stem cells blood
4 chr1:47676400-47679600 Enhancers Right Atrium heart
5 chr1:47676800-47679200 Enhancers Left Ventricle heart
6 chr1:47677000-47679200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:47677200-47679200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr1:47677200-47679200 Enhancers Lung lung
9 chr1:47677200-47679400 Enhancers Spleen Spleen
10 chr1:47677600-47679200 Enhancers Adipose Nuclei Adipose
11 chr1:47677600-47679600 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
12 chr1:47677600-47681800 Weak transcription Placenta Amnion Placenta Amnion
13 chr1:47677800-47681600 Enhancers Primary hematopoietic stem cells short term culture blood
14 chr1:47678000-47679200 Weak transcription Placenta Placenta
15 chr1:47678000-47679200 Bivalent Enhancer HepG2 liver
16 chr1:47678200-47680000 Weak transcription Monocytes-CD14+_RO01746 blood
17 chr1:47678200-47680200 Weak transcription Primary monocytes fromperipheralblood blood
18 chr1:47678200-47681200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
19 chr1:47678200-47681600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
20 chr1:47678800-47679600 Flanking Active TSS K562 blood
21 chr1:47679000-47679400 Bivalent Enhancer Fetal Muscle Trunk muscle

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