Variant report

Variant rs201804712
Chromosome Location chr16:70232937-70232938
allele -/GTTT
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:70226600-70252600 Weak transcription Adipose Nuclei Adipose
2 chr16:70229800-70233800 Enhancers Fetal Adrenal Gland Adrenal Gland
3 chr16:70231000-70233400 Enhancers HUVEC blood vessel
4 chr16:70231000-70233600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr16:70231200-70252000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr16:70231400-70258600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr16:70232000-70233800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr16:70232200-70233200 Enhancers Fetal Muscle Trunk muscle
9 chr16:70232200-70233600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr16:70232400-70233000 Weak transcription Primary hematopoietic stem cells blood
11 chr16:70232400-70284800 Weak transcription Spleen Spleen
12 chr16:70232600-70233200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr16:70232600-70233400 Enhancers Fetal Lung lung
14 chr16:70232600-70241400 Weak transcription Primary hematopoietic stem cells short term culture blood
15 chr16:70232800-70233200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr16:70232800-70233600 Enhancers HepG2 liver

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