Variant report

Variant rs17545166
Chromosome Location chr2:111660562-111660563
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:111632000-111662000 Weak transcription H1 Cell Line embryonic stem cell
2 chr2:111652000-111662200 Weak transcription H9 Cell Line embryonic stem cell
3 chr2:111658000-111662000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr2:111658400-111662400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr2:111658800-111665000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr2:111658800-111665200 Weak transcription Fetal Intestine Small intestine
7 chr2:111660000-111660600 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr2:111660000-111662000 Enhancers Colon Smooth Muscle Colon
9 chr2:111660000-111663600 Enhancers Fetal Muscle Leg muscle
10 chr2:111660200-111663600 Enhancers Fetal Muscle Trunk muscle
11 chr2:111660400-111660600 Enhancers Skeletal Muscle Male skeletal muscle
12 chr2:111660400-111660800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr2:111660400-111660800 Bivalent Enhancer Muscle Satellite Cultured Cells --
14 chr2:111660400-111660800 Enhancers Sigmoid Colon Sigmoid Colon
15 chr2:111660400-111661200 Enhancers Osteobl bone
16 chr2:111660400-111661400 Enhancers Fetal Stomach stomach
17 chr2:111660400-111661600 Enhancers HSMM muscle
18 chr2:111660400-111661800 Enhancers Brain Inferior Temporal Lobe brain

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