Variant report

Variant rs572330008
Chromosome Location chr12:105864025-105864026
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:105860600-105866200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr12:105861400-105864400 Enhancers HSMMtube muscle
3 chr12:105862600-105865000 Enhancers HSMM muscle
4 chr12:105862800-105864200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr12:105863000-105864200 Enhancers Muscle Satellite Cultured Cells --
6 chr12:105863000-105864200 Enhancers Aorta Aorta
7 chr12:105863200-105884200 Weak transcription Right Atrium heart
8 chr12:105863400-105864200 Weak transcription Fetal Heart heart
9 chr12:105863800-105864800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr12:105864000-105864200 Enhancers Right Ventricle heart
11 chr12:105864000-105864200 Active TSS HUVEC blood vessel
12 chr12:105864000-105864400 ZNF genes & repeats Fetal Kidney kidney
13 chr12:105864000-105864600 Enhancers Fetal Brain Male brain
14 chr12:105864000-105866800 Weak transcription Fetal Adrenal Gland Adrenal Gland
15 chr12:105864000-105868400 Weak transcription NH-A brain

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