Variant report

Variant rs35755918
Chromosome Location chr4:10690918-10690919
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:10683600-10691600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr4:10686600-10692800 Enhancers Primary B cells from peripheral blood blood
3 chr4:10686800-10691000 Weak transcription Spleen Spleen
4 chr4:10688800-10693400 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr4:10689200-10693600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr4:10689600-10692600 Enhancers Primary B cells from cord blood blood
7 chr4:10689600-10693400 Weak transcription Ovary ovary
8 chr4:10690000-10692600 Enhancers Primary hematopoietic stem cells blood
9 chr4:10690000-10692600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr4:10690600-10692000 Enhancers Thymus Thymus
11 chr4:10690600-10692800 Enhancers Primary monocytes fromperipheralblood blood
12 chr4:10690800-10691000 Enhancers Primary Natural Killer cells fromperipheralblood blood
13 chr4:10690800-10691000 Flanking Active TSS GM12878-XiMat blood
14 chr4:10690800-10691200 Enhancers Fetal Adrenal Gland Adrenal Gland
15 chr4:10690800-10691600 Enhancers Monocytes-CD14+_RO01746 blood
16 chr4:10690800-10692000 Enhancers Fetal Thymus thymus

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