Variant report

Variant rs73336691
Chromosome Location chr5:177877707-177877708
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177856800-177887200 Weak transcription Right Atrium heart
2 chr5:177871800-177880600 Weak transcription Fetal Thymus thymus
3 chr5:177874600-177888200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr5:177876200-177877800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr5:177876200-177877800 Enhancers HUES6 Cell Line embryonic stem cell
6 chr5:177876200-177878000 Enhancers Primary monocytes fromperipheralblood blood
7 chr5:177876400-177877800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
8 chr5:177876400-177877800 Flanking Active TSS K562 blood
9 chr5:177876800-177877800 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr5:177877000-177881600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr5:177877400-177879200 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr5:177877600-177877800 Bivalent Enhancer Monocytes-CD14+_RO01746 blood
13 chr5:177877600-177880000 Weak transcription H1 Cell Line embryonic stem cell
14 chr5:177877600-177880200 Weak transcription ES-I3 Cell Line embryonic stem cell
15 chr5:177877600-177880200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr5:177877600-177881400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
17 chr5:177877600-177894200 Weak transcription Spleen Spleen

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