Variant report

Variant rs62580597
Chromosome Location chr9:139674978-139674979
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139668200-139682400 Weak transcription Right Atrium heart
2 chr9:139673400-139682000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr9:139674000-139675000 Enhancers K562 blood
4 chr9:139674200-139675400 Enhancers Colonic Mucosa Colon
5 chr9:139674400-139675000 Enhancers Fetal Intestine Small intestine
6 chr9:139674400-139676000 Enhancers Fetal Intestine Large intestine
7 chr9:139674400-139676000 Enhancers HepG2 liver
8 chr9:139674400-139676600 Enhancers Rectal Mucosa Donor 31 rectum
9 chr9:139674600-139675200 Enhancers Placenta Placenta
10 chr9:139674800-139675200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr9:139674800-139678600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr9:139674800-139682000 Weak transcription A549 lung

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