Variant report

Variant rs55909699
Chromosome Location chr10:4910150-4910151
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:4892200-4917800 Weak transcription Primary T cells from cord blood blood
2 chr10:4893000-4925000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr10:4899800-4913000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr10:4903400-4924800 Weak transcription A549 lung
5 chr10:4908600-4910600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr10:4908800-4944200 Weak transcription Adipose Nuclei Adipose
7 chr10:4909000-4910600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr10:4909200-4912800 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr10:4909400-4910600 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr10:4909400-4910800 Flanking Active TSS K562 blood
11 chr10:4909600-4910400 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr10:4909600-4910400 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr10:4909600-4910400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr10:4909600-4911000 Enhancers Fetal Heart heart
15 chr10:4909800-4910200 Flanking Active TSS HUVEC blood vessel
16 chr10:4909800-4910400 Enhancers Left Ventricle heart
17 chr10:4909800-4910600 Enhancers Aorta Aorta
18 chr10:4910000-4910200 Flanking Active TSS HepG2 liver
19 chr10:4910000-4914600 Weak transcription Liver Liver

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