Variant report

Variant rs9261525
Chromosome Location chr6:30118128-30118129
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:30112800-30119200 Strong transcription Placenta Placenta
2 chr6:30112800-30120800 Weak transcription Sigmoid Colon Sigmoid Colon
3 chr6:30113000-30119600 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr6:30113800-30118600 Weak transcription Fetal Intestine Large intestine
5 chr6:30116000-30121800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr6:30116400-30118600 Weak transcription Fetal Intestine Small intestine
7 chr6:30116400-30119400 Enhancers HepG2 liver
8 chr6:30117000-30119200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr6:30117200-30119400 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr6:30117200-30122000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr6:30117800-30119000 Bivalent Enhancer Osteobl bone
12 chr6:30117800-30119400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr6:30117800-30121600 Enhancers Primary hematopoietic stem cells blood
14 chr6:30118000-30118400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr6:30118000-30119000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr6:30118000-30119000 Bivalent Enhancer NHDF-Ad bronchial
17 chr6:30118000-30120600 Enhancers K562 blood

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