Variant report

Variant rs59358880
Chromosome Location chr16:71860936-71860937
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:71843800-71861600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr16:71844200-71862200 Weak transcription Monocytes-CD14+_RO01746 blood
3 chr16:71844800-71862000 Weak transcription Primary monocytes fromperipheralblood blood
4 chr16:71851200-71862200 Weak transcription Fetal Stomach stomach
5 chr16:71851200-71866400 Weak transcription HSMMtube muscle
6 chr16:71852200-71861600 Weak transcription Esophagus oesophagus
7 chr16:71852200-71861800 Weak transcription Fetal Muscle Leg muscle
8 chr16:71852200-71861800 Weak transcription HSMM muscle
9 chr16:71852200-71866000 Weak transcription Skeletal Muscle Male skeletal muscle
10 chr16:71852400-71863000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr16:71852800-71864000 Weak transcription Osteobl bone
12 chr16:71854800-71861200 Weak transcription Skeletal Muscle Female skeletal muscle
13 chr16:71856000-71861400 Weak transcription Psoas Muscle Psoas
14 chr16:71858000-71863400 Weak transcription Primary T cells from cord blood blood
15 chr16:71860600-71861000 Enhancers Primary T helper naive cells fromperipheralblood blood
16 chr16:71860600-71861000 Flanking Active TSS K562 blood
17 chr16:71860800-71863800 Weak transcription GM12878-XiMat blood

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