Variant report

Variant rs463652
Chromosome Location chr21:41161367-41161368
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:41160000-41163600 Enhancers Fetal Heart heart
2 chr21:41160200-41161400 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr21:41160400-41161400 Enhancers Placenta Placenta
4 chr21:41160600-41161400 Enhancers Pancreas Pancrea
5 chr21:41160600-41161400 Active TSS Right Atrium heart
6 chr21:41160600-41163200 Weak transcription Colon Smooth Muscle Colon
7 chr21:41160800-41161400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr21:41160800-41162000 Weak transcription Fetal Brain Female brain
9 chr21:41160800-41163000 Weak transcription Rectal Smooth Muscle rectum
10 chr21:41161000-41161400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr21:41161000-41161400 Enhancers Fetal Kidney kidney
12 chr21:41161000-41171000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
13 chr21:41161200-41161400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr21:41161200-41161400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
15 chr21:41161200-41161400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr21:41161200-41162600 Enhancers Left Ventricle heart
17 chr21:41161200-41163600 Weak transcription Fetal Stomach stomach
18 chr21:41161200-41168000 Weak transcription Right Ventricle heart

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