Variant report

Variant nsv979607
Chromosome Location chr22:23262334-23266166
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:23249800-23270800 Strong transcription Right Atrium heart
2 chr22:23254000-23268800 Weak transcription Spleen Spleen
3 chr22:23257200-23268000 Weak transcription Primary hematopoietic stem cells short term culture blood
4 chr22:23257800-23264200 Weak transcription GM12878-XiMat blood
5 chr22:23259400-23290200 Enhancers Primary B cells from peripheral blood blood
6 chr22:23261800-23263000 Enhancers Primary B cells from cord blood blood
7 chr22:23263000-23263600 Weak transcription Primary B cells from cord blood blood
8 chr22:23263600-23289400 Enhancers Primary B cells from cord blood blood
9 chr22:23264200-23264400 Enhancers GM12878-XiMat blood
10 chr22:23264400-23265200 Weak transcription GM12878-XiMat blood
11 chr22:23265200-23267400 Enhancers GM12878-XiMat blood
12 chr22:23265800-23267000 Enhancers Primary T helper 17 cells PMA-I stimulated --
13 chr22:23266000-23266600 Enhancers Fetal Intestine Small intestine
14 chr22:23266000-23266800 Enhancers Primary Natural Killer cells fromperipheralblood blood
15 chr22:23266000-23269200 Enhancers Fetal Intestine Large intestine
16 chr22:23266000-23269800 Enhancers Monocytes-CD14+_RO01746 blood

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