Variant report

Variant rs561046816
Chromosome Location chr14:22381607-22381608
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:22380000-22382200 Enhancers Primary T cells from cord blood blood
2 chr14:22380200-22383200 Enhancers Primary T helper cells PMA-I stimulated --
3 chr14:22380400-22381800 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr14:22380400-22382400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr14:22380400-22382400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr14:22380400-22386200 Enhancers HUVEC blood vessel
7 chr14:22380600-22381800 Weak transcription Primary T helper naive cells fromperipheralblood blood
8 chr14:22380600-22381800 Weak transcription Primary T killer memory cells from peripheral blood blood
9 chr14:22380600-22386600 Weak transcription Gastric stomach
10 chr14:22380800-22382000 Weak transcription Primary T helper naive cells from peripheral blood blood
11 chr14:22380800-22383400 Weak transcription Primary B cells from cord blood blood
12 chr14:22381000-22382000 Weak transcription Primary T cells fromperipheralblood blood
13 chr14:22381000-22382000 Weak transcription Primary T helper cells fromperipheralblood blood
14 chr14:22381200-22382200 Weak transcription Thymus Thymus
15 chr14:22381400-22381800 Weak transcription Fetal Thymus thymus
16 chr14:22381600-22386200 Weak transcription Primary hematopoietic stem cells blood

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