Variant report

Variant rs10239268
Chromosome Location chr7:50876443-50876444
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:50862200-50889000 Weak transcription Right Atrium heart
2 chr7:50868000-50880000 Weak transcription Left Ventricle heart
3 chr7:50870200-50878000 Weak transcription Spleen Spleen
4 chr7:50871400-50879600 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr7:50871600-50879800 Weak transcription H1 Cell Line embryonic stem cell
6 chr7:50873800-50879400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr7:50874000-50879000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr7:50874000-50879800 Weak transcription A549 lung
9 chr7:50874400-50879800 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr7:50875200-50880200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr7:50875600-50880400 Weak transcription Osteobl bone
12 chr7:50875800-50876800 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr7:50876000-50876600 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr7:50876000-50876800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr7:50876000-50877000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr7:50876000-50877000 Enhancers HMEC breast
17 chr7:50876000-50879400 Weak transcription Hela-S3 cervix
18 chr7:50876400-50880400 Weak transcription Esophagus oesophagus
19 chr7:50876400-50880600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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