Variant report

Variant rs17026547
Chromosome Location chr2:40948260-40948261
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:40944600-40948600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr2:40944600-40948800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:40944600-40949000 Weak transcription Osteobl bone
4 chr2:40944600-40949600 Weak transcription Esophagus oesophagus
5 chr2:40944800-40948400 Weak transcription NHEK skin
6 chr2:40944800-40948600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:40944800-40948600 Weak transcription HMEC breast
8 chr2:40945200-40948600 Weak transcription NHDF-Ad bronchial
9 chr2:40945600-40948600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr2:40946000-40948600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr2:40946600-40948800 Weak transcription HSMM muscle
12 chr2:40946800-40948600 Weak transcription HSMMtube muscle
13 chr2:40947000-40951200 Weak transcription Colon Smooth Muscle Colon
14 chr2:40947000-40952400 Weak transcription Rectal Smooth Muscle rectum
15 chr2:40947400-40948400 Weak transcription Muscle Satellite Cultured Cells --

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