Variant report

Variant rs72831377
Chromosome Location chr16:81257141-81257142
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:81249000-81257200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr16:81254200-81258600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr16:81256200-81257400 Enhancers K562 blood
4 chr16:81256200-81257600 Enhancers Duodenum Mucosa Duodenum
5 chr16:81256400-81257800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr16:81256400-81259000 Enhancers Fetal Intestine Small intestine
7 chr16:81256400-81259000 Enhancers Placenta Placenta
8 chr16:81256600-81257400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr16:81256800-81257200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr16:81256800-81257200 Flanking Active TSS Fetal Heart heart
11 chr16:81256800-81257200 Enhancers Gastric stomach
12 chr16:81256800-81257400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr16:81256800-81257400 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr16:81256800-81257400 Enhancers Fetal Kidney kidney
15 chr16:81256800-81257600 Enhancers Fetal Intestine Large intestine
16 chr16:81256800-81257600 Bivalent Enhancer HepG2 liver

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