Variant report

Variant rs148021269
Chromosome Location chr5:17445902-17445903
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:17430800-17463800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:17442400-17446200 Flanking Active TSS Primary neutrophils fromperipheralblood blood
3 chr5:17442600-17448400 Weak transcription Osteobl bone
4 chr5:17444000-17446200 Enhancers Stomach Mucosa stomach
5 chr5:17444200-17446200 Enhancers A549 lung
6 chr5:17444200-17446400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr5:17444400-17446000 Enhancers Rectal Mucosa Donor 29 rectum
8 chr5:17444400-17446400 Enhancers Monocytes-CD14+_RO01746 blood
9 chr5:17445000-17446200 Enhancers Rectal Mucosa Donor 31 rectum
10 chr5:17445200-17448000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr5:17445400-17446200 Enhancers Primary monocytes fromperipheralblood blood
12 chr5:17445400-17446200 Enhancers Gastric stomach
13 chr5:17445400-17446200 Enhancers Sigmoid Colon Sigmoid Colon
14 chr5:17445600-17446200 Flanking Active TSS Primary B cells from cord blood blood

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