Variant report

Variant rs9495464
Chromosome Location chr6:139709391-139709392
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:139700600-139709400 Weak transcription Fetal Intestine Large intestine
2 chr6:139700600-139713800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr6:139706200-139713800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr6:139706400-139713800 Weak transcription Osteobl bone
5 chr6:139708000-139709600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr6:139708000-139709600 Weak transcription K562 blood
7 chr6:139708000-139711600 Weak transcription Skeletal Muscle Female skeletal muscle
8 chr6:139708000-139713000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr6:139708200-139709600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr6:139708400-139713800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr6:139709000-139709600 Enhancers Duodenum Mucosa Duodenum
12 chr6:139709000-139710200 Enhancers Liver Liver
13 chr6:139709000-139710600 Enhancers HepG2 liver

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