Variant report

Variant rs66993685
Chromosome Location chr2:64267898-64267899
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:64251200-64273200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr2:64266000-64268400 Enhancers Primary T helper naive cells fromperipheralblood blood
3 chr2:64266200-64268000 Enhancers Primary T helper cells fromperipheralblood blood
4 chr2:64266400-64268200 Enhancers Primary T helper naive cells from peripheral blood blood
5 chr2:64266600-64268000 Enhancers Primary T cells fromperipheralblood blood
6 chr2:64266600-64268000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
7 chr2:64266800-64268000 Enhancers Primary T regulatory cells fromperipheralblood blood
8 chr2:64266800-64268000 Enhancers Primary T killer naive cells fromperipheralblood blood
9 chr2:64266800-64268200 Enhancers Fetal Thymus thymus
10 chr2:64267000-64268000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr2:64267000-64268000 Enhancers HUVEC blood vessel
12 chr2:64267000-64268200 Flanking Active TSS Primary T cells from cord blood blood
13 chr2:64267000-64268200 Enhancers Primary T killer memory cells from peripheral blood blood
14 chr2:64267600-64268000 Enhancers Primary monocytes fromperipheralblood blood
15 chr2:64267600-64268000 Enhancers HMEC breast
16 chr2:64267800-64268200 Enhancers Primary T helper cells PMA-I stimulated --

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