Variant report

Variant rs11571890
Chromosome Location chr6:44353901-44353902
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:44341800-44354600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr6:44346600-44354200 Weak transcription HepG2 liver
3 chr6:44348800-44354400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr6:44349000-44354200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr6:44350000-44354200 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr6:44350000-44354600 Weak transcription Adipose Nuclei Adipose
7 chr6:44350200-44354200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr6:44350200-44354200 Weak transcription Fetal Adrenal Gland Adrenal Gland
9 chr6:44350600-44354400 Weak transcription Monocytes-CD14+_RO01746 blood
10 chr6:44350800-44354800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr6:44351000-44354200 Weak transcription Fetal Muscle Leg muscle
12 chr6:44351000-44354400 Weak transcription Primary monocytes fromperipheralblood blood
13 chr6:44352000-44354800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr6:44352200-44354200 Weak transcription HSMMtube muscle
15 chr6:44352400-44354200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr6:44353200-44354600 Weak transcription Aorta Aorta
17 chr6:44353600-44354400 Enhancers Liver Liver

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