Variant report

Variant rs73656514
Chromosome Location chr9:98443821-98443822
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:98441400-98446400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr9:98442400-98446200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr9:98443600-98444400 Enhancers Primary T helper cells fromperipheralblood blood
4 chr9:98443600-98444600 Bivalent Enhancer Primary T cells fromperipheralblood blood
5 chr9:98443600-98444600 Enhancers Primary T helper naive cells from peripheral blood blood
6 chr9:98443600-98444600 Enhancers Primary T helper naive cells fromperipheralblood blood
7 chr9:98443600-98444600 Enhancers Primary T helper 17 cells PMA-I stimulated --
8 chr9:98443800-98444400 Enhancers Primary T killer memory cells from peripheral blood blood
9 chr9:98443800-98444600 Enhancers Primary T cells from cord blood blood
10 chr9:98443800-98444600 Enhancers Primary T helper cells PMA-I stimulated --
11 chr9:98443800-98444600 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
12 chr9:98443800-98444600 Enhancers Primary T killer naive cells fromperipheralblood blood
13 chr9:98443800-98444800 Enhancers Primary T helper memory cells from peripheral blood 2 blood
14 chr9:98443800-98444800 Enhancers Primary T helper memory cells from peripheral blood 1 blood

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