Variant report

Variant rs74078850
Chromosome Location chr12:41834560-41834561
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:41829600-41860600 Weak transcription Aorta Aorta
2 chr12:41831400-41838400 Active TSS Brain Germinal Matrix brain
3 chr12:41831800-41834600 Active TSS Fetal Brain Female brain
4 chr12:41832200-41836800 Weak transcription Brain Substantia Nigra brain
5 chr12:41833000-41835200 Enhancers Brain Cingulate Gyrus brain
6 chr12:41833200-41836400 Weak transcription Fetal Brain Male brain
7 chr12:41833600-41834800 Weak transcription Fetal Kidney kidney
8 chr12:41833800-41835000 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr12:41833800-41836800 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr12:41833800-41837600 Weak transcription Brain Hippocampus Middle brain
11 chr12:41834000-41834600 Enhancers Pancreatic Islets Pancreatic Islet
12 chr12:41834000-41837000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr12:41834000-41837800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr12:41834000-41838000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr12:41834200-41836800 Weak transcription HUES48 Cell Line embryonic stem cell
16 chr12:41834400-41834600 Enhancers Brain Inferior Temporal Lobe brain
17 chr12:41834400-41835000 Enhancers Colon Smooth Muscle Colon

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