Variant report

Variant rs11111589
Chromosome Location chr12:103851528-103851529
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:103848200-103851800 Enhancers Primary B cells from peripheral blood blood
2 chr12:103848400-103851600 Enhancers Primary T helper cells fromperipheralblood blood
3 chr12:103848400-103851800 Enhancers Primary B cells from cord blood blood
4 chr12:103848400-103851800 Enhancers Primary T helper memory cells from peripheral blood 2 blood
5 chr12:103848400-103853200 Enhancers Dnd41 blood
6 chr12:103848600-103851800 Enhancers Primary T helper cells PMA-I stimulated --
7 chr12:103848600-103852200 Enhancers Primary T cells from cord blood blood
8 chr12:103849400-103852400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr12:103850400-103851800 Enhancers Brain Germinal Matrix brain
10 chr12:103850800-103852800 Enhancers Fetal Brain Male brain
11 chr12:103851000-103852000 Enhancers Fetal Brain Female brain
12 chr12:103851200-103852400 Enhancers Cortex derived primary cultured neurospheres brain
13 chr12:103851400-103851600 Enhancers Primary T helper 17 cells PMA-I stimulated --
14 chr12:103851400-103852000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
15 chr12:103851400-103853400 Weak transcription Thymus Thymus
16 chr12:103851400-103855400 Weak transcription GM12878-XiMat blood

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