Variant report

Variant rs10241929
Chromosome Location chr7:18711303-18711304
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:18645400-18721000 Weak transcription Psoas Muscle Psoas
2 chr7:18678400-18721200 Weak transcription Brain Substantia Nigra brain
3 chr7:18688400-18715200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr7:18688800-18746400 Weak transcription Primary hematopoietic stem cells blood
5 chr7:18689400-18713200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr7:18696200-18715000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
7 chr7:18698000-18743400 Weak transcription HSMMtube muscle
8 chr7:18699600-18776000 Weak transcription Aorta Aorta
9 chr7:18703600-18713800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr7:18709200-18711600 Strong transcription Primary monocytes fromperipheralblood blood
11 chr7:18709800-18715800 Strong transcription Primary B cells from cord blood blood
12 chr7:18710600-18711400 Enhancers NHEK skin
13 chr7:18710600-18711600 Enhancers HMEC breast
14 chr7:18710800-18711600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr7:18711000-18711600 Strong transcription Primary B cells from peripheral blood blood
16 chr7:18711200-18711400 Strong transcription Monocytes-CD14+_RO01746 blood

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