Variant report

Variant rs578055003
Chromosome Location chr10:43571392-43571393
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:43554400-43572000 Weak transcription Right Atrium heart
2 chr10:43562800-43571800 Weak transcription Esophagus oesophagus
3 chr10:43563000-43572000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr10:43570200-43571400 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr10:43571000-43572000 Bivalent Enhancer Fetal Stomach stomach
6 chr10:43571200-43571400 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
7 chr10:43571200-43571400 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr10:43571200-43571400 Bivalent/Poised TSS Skeletal Muscle Male skeletal muscle
9 chr10:43571200-43571400 Bivalent/Poised TSS Spleen Spleen
10 chr10:43571200-43571400 Enhancers A549 lung
11 chr10:43571200-43571800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
12 chr10:43571200-43572000 Bivalent Enhancer Colonic Mucosa Colon

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