Variant report

Variant rs12292529
Chromosome Location chr11:71456512-71456513
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:71449600-71459400 Weak transcription Fetal Intestine Small intestine
2 chr11:71451000-71464200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr11:71454400-71456800 Enhancers Stomach Mucosa stomach
4 chr11:71456200-71456600 Enhancers Pancreas Pancrea
5 chr11:71456200-71456800 Bivalent Enhancer Duodenum Mucosa Duodenum
6 chr11:71456400-71456600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:71456400-71456800 Enhancers Rectal Mucosa Donor 31 rectum
8 chr11:71456400-71456800 Enhancers NHEK skin
9 chr11:71456400-71457000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr11:71456400-71457200 Enhancers K562 blood
11 chr11:71456400-71457400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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