Variant report

Variant rs17099793
Chromosome Location chr1:77458677-77458678
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77456200-77460400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr1:77456400-77460600 Weak transcription NHEK skin
3 chr1:77456600-77459200 Enhancers Ovary ovary
4 chr1:77456800-77472400 Weak transcription Aorta Aorta
5 chr1:77458200-77458800 Enhancers Small Intestine intestine
6 chr1:77458400-77460200 Enhancers Cortex derived primary cultured neurospheres brain
7 chr1:77458600-77459000 Enhancers Duodenum Smooth Muscle Duodenum
8 chr1:77458600-77459000 Enhancers Fetal Stomach stomach
9 chr1:77458600-77459400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr1:77458600-77459800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain

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