Variant report

Variant rs6579914
Chromosome Location chr5:151333627-151333628
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:151327800-151335000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:151328200-151334000 Weak transcription Primary T helper naive cells fromperipheralblood blood
3 chr5:151329800-151337400 Weak transcription Fetal Muscle Leg muscle
4 chr5:151330600-151335000 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
5 chr5:151330800-151333800 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
6 chr5:151332200-151333800 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
7 chr5:151332600-151335200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr5:151332800-151335200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
9 chr5:151333000-151338200 Enhancers Primary T helper 17 cells PMA-I stimulated --
10 chr5:151333400-151334400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr5:151333400-151338000 Enhancers Primary T helper cells fromperipheralblood blood
12 chr5:151333600-151335200 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr5:151333600-151338000 Enhancers Primary T helper cells PMA-I stimulated --

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