Variant report

Variant rs7038656
Chromosome Location chr9:139675829-139675830
allele C/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 chr9:139674400-139676000 Enhancers Fetal Intestine Large intestine
4 chr9:139674400-139676000 Enhancers HepG2 liver
5 chr9:139674400-139676600 Enhancers Rectal Mucosa Donor 31 rectum
6 chr9:139674800-139678600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr9:139674800-139682000 Weak transcription A549 lung
8 chr9:139675200-139678600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr9:139675400-139682000 Weak transcription Colonic Mucosa Colon
10 chr9:139675600-139676000 Enhancers K562 blood
11 chr9:139675600-139677000 Weak transcription Fetal Intestine Small intestine
12 chr9:139675800-139676000 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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