Variant report

Variant rs539162871
Chromosome Location chr6:167629482-167629483
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167624600-167632800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:167625600-167630000 Weak transcription Rectal Smooth Muscle rectum
3 chr6:167626200-167635000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr6:167626600-167631000 Weak transcription Placenta Amnion Placenta Amnion
5 chr6:167628000-167630400 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr6:167628200-167637200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr6:167628200-167638600 Weak transcription Fetal Brain Female brain
8 chr6:167628800-167630400 Enhancers Fetal Intestine Large intestine
9 chr6:167629000-167630000 Enhancers Fetal Intestine Small intestine
10 chr6:167629000-167630400 Enhancers Stomach Mucosa stomach
11 chr6:167629000-167632400 Enhancers Liver Liver
12 chr6:167629200-167632200 Weak transcription Fetal Brain Male brain
13 chr6:167629400-167630000 Active TSS HepG2 liver

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