Variant report

Variant rs13267552
Chromosome Location chr8:11812454-11812455
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11807600-11812600 Weak transcription Right Atrium heart
2 chr8:11810800-11813000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr8:11810800-11813000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr8:11811400-11812800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr8:11811600-11812600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr8:11812000-11813000 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr8:11812200-11812600 Enhancers Stomach Smooth Muscle stomach
8 chr8:11812200-11813800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr8:11812200-11814200 Enhancers Fetal Heart heart
10 chr8:11812400-11812600 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr8:11812400-11812600 Enhancers Brain Inferior Temporal Lobe brain
12 chr8:11812400-11812600 Enhancers Colon Smooth Muscle Colon
13 chr8:11812400-11812600 Enhancers Rectal Smooth Muscle rectum
14 chr8:11812400-11813000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
15 chr8:11812400-11813000 Enhancers Right Ventricle heart
16 chr8:11812400-11813400 Bivalent Enhancer Fetal Stomach stomach

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