Variant report

Variant rs12525768
Chromosome Location chr6:15223452-15223453
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:15212000-15227600 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr6:15219200-15223800 Weak transcription H1 Cell Line embryonic stem cell
3 chr6:15219200-15224000 Weak transcription iPS-20b Cell Line embryonic stem cell
4 chr6:15219400-15224000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr6:15219400-15224200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr6:15222400-15227600 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr6:15222600-15223800 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr6:15222600-15224200 Weak transcription H9 Cell Line embryonic stem cell
9 chr6:15222600-15239400 Weak transcription Right Atrium heart
10 chr6:15222800-15224000 Enhancers Placenta Placenta
11 chr6:15223000-15224200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
12 chr6:15223200-15224000 Flanking Active TSS Primary monocytes fromperipheralblood blood
13 chr6:15223200-15224000 Enhancers Primary neutrophils fromperipheralblood blood
14 chr6:15223200-15224200 Enhancers Primary B cells from cord blood blood
15 chr6:15223400-15223800 Enhancers Primary B cells from peripheral blood blood
16 chr6:15223400-15223800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
17 chr6:15223400-15224000 Enhancers Primary hematopoietic stem cells blood

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