Variant report

Variant rs659879
Chromosome Location chr7:4211390-4211391
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4169200-4228200 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr7:4185000-4227800 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr7:4189200-4217000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr7:4189600-4228400 Weak transcription Fetal Brain Female brain
5 chr7:4191400-4215200 Weak transcription Aorta Aorta
6 chr7:4196400-4216000 Weak transcription Fetal Lung lung
7 chr7:4196400-4219600 Weak transcription Fetal Intestine Large intestine
8 chr7:4199000-4213000 Weak transcription Stomach Smooth Muscle stomach
9 chr7:4202000-4215200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr7:4203000-4213800 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr7:4207200-4216600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr7:4207600-4212600 Weak transcription Pancreas Pancrea
13 chr7:4207800-4213400 Weak transcription Spleen Spleen
14 chr7:4207800-4228800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr7:4208000-4213800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr7:4209200-4211600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
17 chr7:4211000-4212000 Strong transcription Fetal Intestine Small intestine

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