Variant report

Variant rs7384540
Chromosome Location chr7:102257833-102257834
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:102257000-102258000 Enhancers Primary B cells from cord blood blood
2 chr7:102257000-102258000 Enhancers Dnd41 blood
3 chr7:102257000-102258000 Enhancers HUVEC blood vessel
4 chr7:102257200-102258000 Enhancers Primary T cells fromperipheralblood blood
5 chr7:102257200-102259000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr7:102257200-102259800 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr7:102257400-102258000 Enhancers Primary T helper naive cells fromperipheralblood blood
8 chr7:102257400-102259000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr7:102257600-102258000 Enhancers Adipose Nuclei Adipose
10 chr7:102257600-102258000 Enhancers Brain Angular Gyrus brain
11 chr7:102257600-102258000 Enhancers Fetal Heart heart
12 chr7:102257800-102258000 Enhancers Primary B cells from peripheral blood blood
13 chr7:102257800-102258000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr7:102257800-102258000 Enhancers Brain Substantia Nigra brain
15 chr7:102257800-102274600 Weak transcription Fetal Adrenal Gland Adrenal Gland

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