Variant report

Variant rs225714
Chromosome Location chr6:142546938-142546939
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:142535000-142548800 Weak transcription NH-A brain
2 chr6:142535200-142548800 Weak transcription Left Ventricle heart
3 chr6:142535200-142552800 Weak transcription H1 Cell Line embryonic stem cell
4 chr6:142535800-142553400 Weak transcription Thymus Thymus
5 chr6:142536000-142552800 Weak transcription Primary T helper naive cells fromperipheralblood blood
6 chr6:142540200-142548400 Weak transcription Placenta Placenta
7 chr6:142541200-142552800 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr6:142541200-142553200 Weak transcription Primary T cells fromperipheralblood blood
9 chr6:142541200-142553400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr6:142541400-142552800 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr6:142541800-142547000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr6:142541800-142550600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:142541800-142553200 Weak transcription HepG2 liver
14 chr6:142542400-142547600 Weak transcription Fetal Thymus thymus
15 chr6:142542400-142550400 Weak transcription Primary B cells from cord blood blood
16 chr6:142542800-142553600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
17 chr6:142546800-142547000 Enhancers NHLF lung

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