Variant report

Variant rs57110552
Chromosome Location chr6:162910040-162910041
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162907000-162912400 Weak transcription Left Ventricle heart
2 chr6:162907000-162915000 Weak transcription Fetal Muscle Leg muscle
3 chr6:162907400-162931400 Weak transcription Psoas Muscle Psoas
4 chr6:162907600-162914600 Weak transcription Fetal Stomach stomach
5 chr6:162907600-162916000 Weak transcription Rectal Smooth Muscle rectum
6 chr6:162909400-162910600 Enhancers HepG2 liver
7 chr6:162909400-162912000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr6:162909600-162923200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr6:162909800-162910400 Flanking Active TSS Liver Liver
10 chr6:162909800-162912400 Weak transcription Pancreas Pancrea
11 chr6:162909800-162912600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr6:162909800-162922000 Weak transcription Aorta Aorta
13 chr6:162910000-162910800 Enhancers Fetal Lung lung
14 chr6:162910000-162911000 Enhancers Fetal Brain Male brain
15 chr6:162910000-162911200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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