Variant report

Variant rs2376986
Chromosome Location chr20:30210072-30210073
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:30199000-30219600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr20:30199000-30225400 Weak transcription Right Atrium heart
3 chr20:30203400-30210400 Enhancers Placenta Placenta
4 chr20:30208000-30211200 Enhancers HepG2 liver
5 chr20:30208800-30210800 Enhancers Primary hematopoietic stem cells blood
6 chr20:30209000-30211000 Enhancers Primary B cells from peripheral blood blood
7 chr20:30209000-30211200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr20:30209000-30211200 Enhancers Fetal Adrenal Gland Adrenal Gland
9 chr20:30209200-30210200 Enhancers Primary B cells from cord blood blood
10 chr20:30209800-30210200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr20:30209800-30210200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr20:30209800-30211000 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr20:30210000-30210400 Enhancers Fetal Muscle Leg muscle
14 chr20:30210000-30210400 Enhancers Stomach Mucosa stomach
15 chr20:30210000-30210400 Enhancers GM12878-XiMat blood
16 chr20:30210000-30211200 Enhancers Left Ventricle heart
17 chr20:30210000-30211200 Enhancers HUVEC blood vessel

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