Variant report

Variant rs16893687
Chromosome Location chr5:60982841-60982842
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:60979200-60983400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr5:60980400-60983000 Enhancers Brain Hippocampus Middle brain
3 chr5:60981000-60983800 Enhancers Brain Anterior Caudate brain
4 chr5:60981800-60983000 Enhancers Small Intestine intestine
5 chr5:60981800-60984000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr5:60981800-60984000 Enhancers HMEC breast
7 chr5:60982000-60984000 Enhancers HSMMtube muscle
8 chr5:60982400-60983600 Enhancers HUES48 Cell Line embryonic stem cell
9 chr5:60982400-60983600 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr5:60982400-60984000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr5:60982400-60984200 Enhancers Sigmoid Colon Sigmoid Colon
12 chr5:60982400-60987800 Weak transcription Brain Substantia Nigra brain
13 chr5:60982600-60983000 Enhancers Pancreatic Islets Pancreatic Islet
14 chr5:60982600-60983000 Flanking Active TSS Rectal Mucosa Donor 31 rectum
15 chr5:60982600-60983400 Enhancers Fetal Lung lung
16 chr5:60982800-60983000 Enhancers Fetal Intestine Small intestine
17 chr5:60982800-60983200 Bivalent Enhancer Muscle Satellite Cultured Cells --
18 chr5:60982800-60983800 Enhancers HSMM muscle

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