Variant report

Variant rs34691991
Chromosome Location chr7:48465921-48465922
allele A/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 chr7:48461600-48466200 Weak transcription Osteobl bone
3 chr7:48461600-48466600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr7:48461800-48466000 Weak transcription NH-A brain
5 chr7:48464600-48466400 Enhancers NHEK skin
6 chr7:48464600-48469200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr7:48464600-48470000 Strong transcription Primary neutrophils fromperipheralblood blood
8 chr7:48465600-48466200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr7:48465600-48467400 Enhancers HMEC breast
10 chr7:48465800-48466000 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr7:48465800-48466200 Enhancers HUES6 Cell Line embryonic stem cell
12 chr7:48465800-48466200 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr7:48465800-48467200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr7:48465800-48467400 Enhancers Rectal Mucosa Donor 29 rectum

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