Variant report

Variant rs2095252
Chromosome Location chr6:132283588-132283589
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132275600-132299800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr6:132276200-132287400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr6:132276600-132297800 Weak transcription Ovary ovary
4 chr6:132277000-132287800 Weak transcription H1 Cell Line embryonic stem cell
5 chr6:132277200-132287600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr6:132277400-132287600 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr6:132277400-132291200 Weak transcription H9 Cell Line embryonic stem cell
8 chr6:132277400-132305600 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr6:132280000-132284000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr6:132280800-132293800 Weak transcription Rectal Mucosa Donor 31 rectum
11 chr6:132281600-132284800 Weak transcription Stomach Mucosa stomach
12 chr6:132282000-132284600 Weak transcription Stomach Smooth Muscle stomach
13 chr6:132282000-132291400 Weak transcription Fetal Brain Male brain
14 chr6:132282200-132283800 Weak transcription HepG2 liver
15 chr6:132282200-132287400 Weak transcription Osteobl bone
16 chr6:132282200-132287600 Weak transcription Muscle Satellite Cultured Cells --
17 chr6:132282400-132287400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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