Variant report

Variant rs17761197
Chromosome Location chr9:22072730-22072731
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:22053800-22079800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:22055600-22079800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr9:22067400-22073400 Weak transcription Primary T helper cells PMA-I stimulated --
4 chr9:22067600-22073400 Weak transcription Primary T helper naive cells fromperipheralblood blood
5 chr9:22071200-22078800 Weak transcription Dnd41 blood
6 chr9:22072000-22076200 Enhancers Primary T helper memory cells from peripheral blood 1 blood
7 chr9:22072000-22076200 Enhancers Primary T helper 17 cells PMA-I stimulated --
8 chr9:22072000-22076200 Enhancers Primary T helper cells fromperipheralblood blood
9 chr9:22072000-22076400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
10 chr9:22072400-22073200 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
11 chr9:22072400-22074000 Enhancers Primary T cells from cord blood blood
12 chr9:22072400-22075800 Enhancers Primary T helper naive cells from peripheral blood blood
13 chr9:22072600-22073000 Enhancers Adipose Nuclei Adipose
14 chr9:22072600-22076400 Enhancers Primary T killer memory cells from peripheral blood blood

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