Variant report

Variant rs566631474
Chromosome Location chr4:128707703-128707704
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:128705000-128718200 Weak transcription Fetal Heart heart
2 chr4:128705400-128731600 Weak transcription Pancreas Pancrea
3 chr4:128705600-128713400 Weak transcription Fetal Adrenal Gland Adrenal Gland
4 chr4:128706000-128743600 Weak transcription Duodenum Smooth Muscle Duodenum
5 chr4:128706200-128759800 Weak transcription Brain Cingulate Gyrus brain
6 chr4:128706400-128716400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr4:128706400-128716600 Weak transcription Hela-S3 cervix
8 chr4:128706400-128726200 Weak transcription HMEC breast
9 chr4:128706400-128729800 Weak transcription NHEK skin
10 chr4:128706400-128741600 Weak transcription K562 blood
11 chr4:128706800-128707800 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr4:128707000-128726800 Weak transcription HepG2 liver
13 chr4:128707200-128708000 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr4:128707200-128712800 Weak transcription Pancreatic Islets Pancreatic Islet
15 chr4:128707200-128716600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr4:128707600-128708000 Enhancers Aorta Aorta

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