Variant report

Variant rs9992798
Chromosome Location chr4:10554478-10554479
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:10538400-10578200 Weak transcription GM12878-XiMat blood
2 chr4:10551200-10566000 Weak transcription Primary hematopoietic stem cells short term culture blood
3 chr4:10553800-10556400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr4:10554000-10555800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
5 chr4:10554200-10554600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr4:10554200-10554800 Bivalent Enhancer Duodenum Mucosa Duodenum
7 chr4:10554200-10554800 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr4:10554200-10555400 Enhancers Primary hematopoietic stem cells blood
9 chr4:10554400-10554800 Enhancers HUVEC blood vessel
10 chr4:10554400-10555000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr4:10554400-10572200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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