Variant report

Variant rs571821771
Chromosome Location chr2:112060098-112060099
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:112025600-112116600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
2 chr2:112048800-112069600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr2:112055000-112070600 Weak transcription NHLF lung
4 chr2:112058200-112069600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr2:112058200-112071000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr2:112058600-112068400 Weak transcription HepG2 liver
7 chr2:112059800-112060400 Enhancers HSMMtube muscle
8 chr2:112059800-112060600 Enhancers Left Ventricle heart
9 chr2:112059800-112060800 Enhancers Fetal Thymus thymus
10 chr2:112059800-112061000 Enhancers Dnd41 blood
11 chr2:112059800-112061000 Enhancers HSMM muscle
12 chr2:112060000-112060800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --

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