Variant report

Variant rs56404532
Chromosome Location chr1:47986919-47986920
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:47976000-47989200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:47984200-47988200 Enhancers Fetal Adrenal Gland Adrenal Gland
3 chr1:47985400-47987400 Weak transcription NH-A brain
4 chr1:47985800-47987200 Enhancers Pancreas Pancrea
5 chr1:47986200-47987600 Enhancers Stomach Mucosa stomach
6 chr1:47986600-47987600 Enhancers Right Atrium heart
7 chr1:47986600-47988200 Enhancers Aorta Aorta
8 chr1:47986600-47988800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr1:47986600-47988800 Enhancers Fetal Kidney kidney
10 chr1:47986600-47989200 Enhancers Liver Liver
11 chr1:47986800-47987000 Bivalent Enhancer Brain Dorsolateral Prefrontal Cortex brain
12 chr1:47986800-47987200 Enhancers Fetal Lung lung
13 chr1:47986800-47987600 Enhancers Rectal Mucosa Donor 31 rectum
14 chr1:47986800-47987800 Enhancers Osteobl bone
15 chr1:47986800-47989400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --

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