Variant report

Variant rs12863734
Chromosome Location chr13:86370571-86370572
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:86335000-86372800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr13:86362400-86371000 Weak transcription Placenta Amnion Placenta Amnion
3 chr13:86366400-86370600 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr13:86367000-86372200 Weak transcription Fetal Muscle Trunk muscle
5 chr13:86367200-86370800 Weak transcription Stomach Smooth Muscle stomach
6 chr13:86367200-86371200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr13:86368800-86371400 Weak transcription Rectal Mucosa Donor 31 rectum
8 chr13:86369600-86370600 ZNF genes & repeats Fetal Lung lung
9 chr13:86369800-86370600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr13:86370000-86371000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr13:86370000-86371600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr13:86370000-86373400 Active TSS Duodenum Mucosa Duodenum
13 chr13:86370000-86373600 Active TSS Fetal Intestine Small intestine
14 chr13:86370200-86373600 Active TSS Fetal Intestine Large intestine
15 chr13:86370400-86370800 Enhancers HUES48 Cell Line embryonic stem cell
16 chr13:86370400-86373600 Active TSS hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr13:86370400-86373600 Active TSS Fetal Stomach stomach

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