Variant report

Variant rs13136260
Chromosome Location chr4:110657248-110657249
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:110651600-110662000 Weak transcription HepG2 liver
2 chr4:110651800-110657800 Weak transcription Small Intestine intestine
3 chr4:110651800-110669400 Weak transcription Spleen Spleen
4 chr4:110652000-110662400 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr4:110652000-110682800 Weak transcription Left Ventricle heart
6 chr4:110652000-110686000 Weak transcription Ovary ovary
7 chr4:110652200-110657600 Weak transcription Duodenum Mucosa Duodenum
8 chr4:110654800-110659200 Enhancers Fetal Intestine Large intestine
9 chr4:110655000-110658400 Enhancers Fetal Intestine Small intestine
10 chr4:110656400-110658400 Enhancers Liver Liver
11 chr4:110656600-110658000 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr4:110656800-110657400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr4:110656800-110657400 Enhancers Fetal Heart heart
14 chr4:110656800-110657400 Flanking Active TSS K562 blood
15 chr4:110656800-110657800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
16 chr4:110656800-110658200 Enhancers Pancreas Pancrea
17 chr4:110657200-110660600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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