Variant report

Variant rs12193728
Chromosome Location chr6:88464738-88464739
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:88456400-88465400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr6:88457800-88482400 Weak transcription Placenta Placenta
3 chr6:88458200-88465600 Weak transcription HepG2 liver
4 chr6:88461800-88466000 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr6:88462800-88466200 Weak transcription Right Atrium heart
6 chr6:88463200-88465600 Weak transcription ES-WA7 Cell Line embryonic stem cell
7 chr6:88463200-88465800 Weak transcription NHLF lung
8 chr6:88463400-88465600 Weak transcription NHDF-Ad bronchial
9 chr6:88464000-88469800 Enhancers Primary monocytes fromperipheralblood blood
10 chr6:88464400-88464800 Flanking Active TSS GM12878-XiMat blood
11 chr6:88464400-88465000 Weak transcription Spleen Spleen
12 chr6:88464400-88466400 Enhancers Primary neutrophils fromperipheralblood blood
13 chr6:88464400-88467600 Enhancers Primary B cells from peripheral blood blood
14 chr6:88464600-88466600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
15 chr6:88464600-88467600 Enhancers Primary hematopoietic stem cells short term culture blood

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