Variant report

Variant rs73878432
Chromosome Location chr22:22749676-22749677
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22748200-22751200 Weak transcription Right Atrium heart
2 chr22:22748600-22749800 Enhancers HepG2 liver
3 chr22:22748600-22752200 Enhancers Primary B cells from cord blood blood
4 chr22:22748600-22753400 Enhancers Dnd41 blood
5 chr22:22748800-22749800 Enhancers GM12878-XiMat blood
6 chr22:22748800-22750000 Enhancers Fetal Intestine Large intestine
7 chr22:22748800-22755200 Enhancers Primary B cells from peripheral blood blood
8 chr22:22749200-22749800 Enhancers Fetal Muscle Leg muscle
9 chr22:22749400-22750000 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
10 chr22:22749400-22750000 Enhancers Fetal Intestine Small intestine
11 chr22:22749400-22752000 Enhancers Thymus Thymus
12 chr22:22749600-22749800 Enhancers Pancreas Pancrea
13 chr22:22749600-22750000 Enhancers Fetal Thymus thymus
14 chr22:22749600-22750200 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr22:22749600-22750800 Enhancers Primary hematopoietic stem cells blood

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