Variant report

Variant rs2888699
Chromosome Location chr2:40948903-40948904
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:40944600-40949000 Weak transcription Osteobl bone
2 chr2:40944600-40949600 Weak transcription Esophagus oesophagus
3 chr2:40947000-40951200 Weak transcription Colon Smooth Muscle Colon
4 chr2:40947000-40952400 Weak transcription Rectal Smooth Muscle rectum
5 chr2:40948400-40949400 Enhancers Muscle Satellite Cultured Cells --
6 chr2:40948400-40949400 Enhancers NHEK skin
7 chr2:40948600-40949200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:40948600-40949200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:40948600-40949400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr2:40948600-40949400 Enhancers HMEC breast
11 chr2:40948600-40949400 Enhancers HSMMtube muscle
12 chr2:40948600-40949600 Enhancers NHDF-Ad bronchial
13 chr2:40948600-40949800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr2:40948800-40949200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr2:40948800-40949200 Enhancers HSMM muscle

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