Variant report

Variant rs34832520
Chromosome Location chr7:48466033-48466034
allele C/T
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 chr7:48461600-48466200 Weak transcription Osteobl bone
3 chr7:48461600-48466600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr7:48464600-48466400 Enhancers NHEK skin
5 chr7:48464600-48469200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr7:48464600-48470000 Strong transcription Primary neutrophils fromperipheralblood blood
7 chr7:48465600-48466200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr7:48465600-48467400 Enhancers HMEC breast
9 chr7:48465800-48466200 Enhancers HUES6 Cell Line embryonic stem cell
10 chr7:48465800-48466200 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr7:48465800-48467200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr7:48465800-48467400 Enhancers Rectal Mucosa Donor 29 rectum
13 chr7:48466000-48467000 Weak transcription ES-I3 Cell Line embryonic stem cell
14 chr7:48466000-48468000 Enhancers NH-A brain

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