Variant report

Variant rs61888261
Chromosome Location chr11:26953208-26953209
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26949000-26953400 Enhancers Colon Smooth Muscle Colon
2 chr11:26951000-26953600 Enhancers HSMMtube muscle
3 chr11:26951400-26953600 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr11:26951600-26953600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr11:26951600-26953600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr11:26951600-26953600 Enhancers HSMM muscle
7 chr11:26952000-26953800 Enhancers NHDF-Ad bronchial
8 chr11:26952400-26953800 Enhancers Fetal Muscle Leg muscle
9 chr11:26952600-26953400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr11:26952600-26953400 Weak transcription Fetal Stomach stomach
11 chr11:26952800-26953400 Enhancers HUES48 Cell Line embryonic stem cell
12 chr11:26953000-26954600 Weak transcription Aorta Aorta
13 chr11:26953200-26953400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr11:26953200-26956800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr11:26953200-26957600 Weak transcription iPS-18 Cell Line embryonic stem cell

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