Variant report

Variant rs552237738
Chromosome Location chr15:76902171-76902172
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:76882200-76991400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
2 chr15:76896800-76915600 Weak transcription Primary B cells from cord blood blood
3 chr15:76898000-76902600 Weak transcription Ovary ovary
4 chr15:76898200-76909600 Weak transcription Left Ventricle heart
5 chr15:76898400-76981000 Weak transcription Pancreas Pancrea
6 chr15:76899800-76904400 Weak transcription Lung lung
7 chr15:76900800-76902600 ZNF genes & repeats Fetal Intestine Large intestine
8 chr15:76900800-76902600 ZNF genes & repeats Fetal Stomach stomach
9 chr15:76901000-76902400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr15:76901000-76902400 Weak transcription Pancreatic Islets Pancreatic Islet
11 chr15:76901000-76902600 ZNF genes & repeats Fetal Intestine Small intestine
12 chr15:76901000-76917200 Weak transcription Gastric stomach
13 chr15:76901200-76902400 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain
14 chr15:76901400-76902800 ZNF genes & repeats Dnd41 blood
15 chr15:76901400-76902800 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
16 chr15:76902000-76903400 Weak transcription Primary T cells from cord blood blood

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