Variant report

Variant rs2149852
Chromosome Location chr13:30926927-30926928
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:30920600-30929400 Weak transcription Spleen Spleen
2 chr13:30921400-30927200 Weak transcription Primary hematopoietic stem cells blood
3 chr13:30921400-30928600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr13:30922200-30928800 Weak transcription Primary T helper naive cells from peripheral blood blood
5 chr13:30922200-30937800 Weak transcription Primary T helper 17 cells PMA-I stimulated --
6 chr13:30922800-30928400 Weak transcription Primary T cells fromperipheralblood blood
7 chr13:30923200-30927200 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
8 chr13:30924600-30940000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
9 chr13:30925400-30927000 Enhancers Thymus Thymus
10 chr13:30925800-30927000 Enhancers Dnd41 blood
11 chr13:30926000-30927000 Enhancers Primary B cells from peripheral blood blood
12 chr13:30926400-30927800 Strong transcription Primary T regulatory cells fromperipheralblood blood
13 chr13:30926600-30927400 ZNF genes & repeats Fetal Thymus thymus
14 chr13:30926800-30927000 Weak transcription Primary B cells from cord blood blood
15 chr13:30926800-30927200 ZNF genes & repeats Aorta Aorta
16 chr13:30926800-30927600 ZNF genes & repeats Primary Natural Killer cells fromperipheralblood blood

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