Variant report

Variant rs4902779
Chromosome Location chr14:70583312-70583313
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:70575600-70586600 Weak transcription Brain Inferior Temporal Lobe brain
2 chr14:70575600-70586800 Weak transcription HSMMtube muscle
3 chr14:70579800-70599400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr14:70580800-70587000 Enhancers Skeletal Muscle Male skeletal muscle
5 chr14:70581600-70586800 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr14:70582200-70587200 Enhancers Skeletal Muscle Female skeletal muscle
7 chr14:70582600-70583400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr14:70582600-70583400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr14:70582800-70584000 Enhancers Fetal Brain Male brain
10 chr14:70582800-70586400 Weak transcription iPS-18 Cell Line embryonic stem cell
11 chr14:70583000-70583400 Enhancers HUES48 Cell Line embryonic stem cell
12 chr14:70583000-70583400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
13 chr14:70583000-70583400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr14:70583000-70585600 Weak transcription Psoas Muscle Psoas
15 chr14:70583200-70583600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr14:70583200-70584000 Enhancers Fetal Brain Female brain

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