Variant report

Variant rs13418028
Chromosome Location chr2:209422648-209422649
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:209419600-209424000 Weak transcription Fetal Intestine Small intestine
2 chr2:209420800-209422800 Enhancers K562 blood
3 chr2:209421200-209423000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr2:209421600-209422800 Enhancers Duodenum Mucosa Duodenum
5 chr2:209421600-209423000 Enhancers Brain Germinal Matrix brain
6 chr2:209421600-209423000 Enhancers Fetal Heart heart
7 chr2:209422200-209423000 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr2:209422400-209422800 Enhancers Colon Smooth Muscle Colon
9 chr2:209422400-209422800 Enhancers Stomach Mucosa stomach
10 chr2:209422600-209422800 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland

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