Variant report

Variant rs9266668
Chromosome Location chr6:31348053-31348054
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:31344400-31348400 Enhancers Adipose Nuclei Adipose
2 chr6:31345000-31361600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:31345600-31353200 Weak transcription Right Atrium heart
4 chr6:31345800-31367400 Weak transcription Gastric stomach
5 chr6:31346200-31348200 Enhancers Colonic Mucosa Colon
6 chr6:31346200-31348200 Enhancers Rectal Mucosa Donor 31 rectum
7 chr6:31346400-31348200 Enhancers Rectal Mucosa Donor 29 rectum
8 chr6:31347600-31348200 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr6:31347800-31348200 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr6:31347800-31348200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
11 chr6:31348000-31348200 Bivalent Enhancer Muscle Satellite Cultured Cells --
12 chr6:31348000-31348200 Bivalent Enhancer NHEK skin
13 chr6:31348000-31350800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr6:31348000-31354200 Weak transcription Lung lung

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