Variant report

Variant rs562485682
Chromosome Location chr2:112060704-112060705
allele A/G
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 chr2:112059800-112060800 Enhancers Fetal Thymus thymus
8 chr2:112059800-112061000 Enhancers Dnd41 blood
9 chr2:112059800-112061000 Enhancers HSMM muscle
10 chr2:112060000-112060800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr2:112060400-112079200 Weak transcription HSMMtube muscle
12 chr2:112060600-112060800 Enhancers NH-A brain

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