Variant report

Variant rs1766698
Chromosome Location chr6:37168367-37168368
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:37158200-37169800 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
2 chr6:37160400-37169000 Weak transcription Primary T cells fromperipheralblood blood
3 chr6:37162600-37169200 Weak transcription Primary T killer memory cells from peripheral blood blood
4 chr6:37162600-37169600 Weak transcription Primary T cells from cord blood blood
5 chr6:37162600-37169600 Weak transcription Primary T helper 17 cells PMA-I stimulated --
6 chr6:37162800-37169200 Weak transcription Primary T helper cells fromperipheralblood blood
7 chr6:37162800-37169600 Weak transcription Dnd41 blood
8 chr6:37167200-37168400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr6:37167200-37179200 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr6:37167400-37168600 Enhancers Primary hematopoietic stem cells blood
11 chr6:37167400-37173400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr6:37167600-37173600 Enhancers Fetal Intestine Small intestine
13 chr6:37167800-37169800 Weak transcription Fetal Intestine Large intestine
14 chr6:37168000-37168400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
15 chr6:37168000-37168400 Enhancers Fetal Thymus thymus
16 chr6:37168000-37173800 Enhancers HepG2 liver
17 chr6:37168200-37168400 Enhancers K562 blood

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