Variant report

Variant rs67591654
Chromosome Location chr7:48466512-48466513
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:48449400-48467800 Weak transcription Primary hematopoietic stem cells blood
2 chr7:48461600-48466600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr7:48464600-48469200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:48464600-48470000 Strong transcription Primary neutrophils fromperipheralblood blood
5 chr7:48465600-48467400 Enhancers HMEC breast
6 chr7:48465800-48467200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr7:48465800-48467400 Enhancers Rectal Mucosa Donor 29 rectum
8 chr7:48466000-48467000 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr7:48466000-48468000 Enhancers NH-A brain
10 chr7:48466200-48466600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr7:48466200-48467400 Enhancers Osteobl bone
12 chr7:48466200-48468000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr7:48466400-48467000 Flanking Active TSS NHEK skin
14 chr7:48466400-48467200 Enhancers Sigmoid Colon Sigmoid Colon

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