Variant report

Variant rs73695668
Chromosome Location chr7:50499987-50499988
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:50486200-50513200 Weak transcription Primary T killer naive cells fromperipheralblood blood
2 chr7:50493400-50505800 Weak transcription Thymus Thymus
3 chr7:50495200-50505800 Weak transcription Fetal Intestine Large intestine
4 chr7:50495200-50513000 Weak transcription Duodenum Mucosa Duodenum
5 chr7:50495200-50517200 Weak transcription Stomach Mucosa stomach
6 chr7:50495600-50513800 Weak transcription HepG2 liver
7 chr7:50496000-50513000 Weak transcription Gastric stomach
8 chr7:50496200-50517600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr7:50496800-50505800 Weak transcription GM12878-XiMat blood
10 chr7:50498000-50506800 Weak transcription Sigmoid Colon Sigmoid Colon
11 chr7:50499200-50500000 Enhancers Cortex derived primary cultured neurospheres brain
12 chr7:50499400-50506000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
13 chr7:50499400-50513000 Weak transcription Psoas Muscle Psoas
14 chr7:50499600-50505400 Weak transcription Fetal Lung lung
15 chr7:50499800-50500000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr7:50499800-50500600 Enhancers HUES48 Cell Line embryonic stem cell
17 chr7:50499800-50506400 Weak transcription Primary B cells from peripheral blood blood

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