Variant report

Variant rs13385706
Chromosome Location chr2:10640549-10640550
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:10634800-10654400 Weak transcription Right Atrium heart
2 chr2:10636800-10642200 Enhancers Fetal Muscle Leg muscle
3 chr2:10638400-10641400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr2:10638600-10641000 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr2:10638600-10641000 Weak transcription Esophagus oesophagus
6 chr2:10638600-10641000 Enhancers NHEK skin
7 chr2:10638800-10642200 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr2:10639600-10641800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:10639800-10642200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr2:10640000-10641000 Enhancers Fetal Thymus thymus
11 chr2:10640000-10641400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr2:10640000-10641600 Enhancers Lung lung
13 chr2:10640000-10642400 Bivalent Enhancer Fetal Muscle Trunk muscle
14 chr2:10640200-10642800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr2:10640200-10645200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr2:10640400-10640600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
17 chr2:10640400-10640600 Enhancers Duodenum Mucosa Duodenum
18 chr2:10640400-10640600 Enhancers Left Ventricle heart
19 chr2:10640400-10642000 Enhancers HMEC breast

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