Variant report

Variant rs17151565
Chromosome Location chr8:10133709-10133710
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:10123000-10138400 Weak transcription Spleen Spleen
2 chr8:10123600-10135400 Weak transcription Fetal Intestine Small intestine
3 chr8:10125600-10136000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr8:10128200-10137000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr8:10128400-10138200 Weak transcription Fetal Brain Female brain
6 chr8:10130400-10144200 Weak transcription Liver Liver
7 chr8:10130600-10137600 Weak transcription Primary T cells from cord blood blood
8 chr8:10131800-10133800 Weak transcription Primary neutrophils fromperipheralblood blood
9 chr8:10132200-10133800 Enhancers Brain Germinal Matrix brain
10 chr8:10133000-10133800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr8:10133200-10133800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
12 chr8:10133400-10133800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr8:10133400-10133800 Enhancers Fetal Brain Male brain
14 chr8:10133400-10134400 Enhancers Cortex derived primary cultured neurospheres brain
15 chr8:10133600-10134000 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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