Variant report

Variant rs12742457
Chromosome Location chr1:168850211-168850212
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:168841600-168850400 Weak transcription Fetal Heart heart
2 chr1:168847000-168858400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:168849200-168850400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr1:168849400-168850400 Enhancers Fetal Intestine Large intestine
5 chr1:168849400-168850400 Enhancers Fetal Intestine Small intestine
6 chr1:168849400-168850400 Enhancers Ovary ovary
7 chr1:168849400-168851000 Enhancers Brain Dorsolateral Prefrontal Cortex brain
8 chr1:168849400-168851200 Enhancers Fetal Stomach stomach
9 chr1:168849600-168850400 Enhancers Rectal Mucosa Donor 31 rectum
10 chr1:168849600-168851800 Enhancers Brain Germinal Matrix brain
11 chr1:168849800-168850400 Enhancers Skeletal Muscle Male skeletal muscle
12 chr1:168849800-168850800 Weak transcription Fetal Brain Male brain
13 chr1:168849800-168852200 Enhancers Fetal Lung lung
14 chr1:168850000-168850400 Enhancers Adipose Nuclei Adipose
15 chr1:168850000-168850400 Enhancers Hela-S3 cervix
16 chr1:168850000-168851000 Weak transcription H1 Cell Line embryonic stem cell
17 chr1:168850200-168850600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
18 chr1:168850200-168857600 Weak transcription Brain Hippocampus Middle brain

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