Variant report

Variant rs9937192
Chromosome Location chr16:79882803-79882804
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:79879600-79885200 Enhancers Thymus Thymus
2 chr16:79879800-79884600 Enhancers Fetal Thymus thymus
3 chr16:79880000-79883400 Weak transcription Primary T cells from cord blood blood
4 chr16:79880600-79884800 Enhancers NHEK skin
5 chr16:79880800-79883600 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr16:79880800-79885200 Enhancers Colon Smooth Muscle Colon
7 chr16:79881400-79883200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr16:79881600-79883000 Weak transcription GM12878-XiMat blood
9 chr16:79881800-79883000 Weak transcription Gastric stomach
10 chr16:79882200-79883400 Enhancers Esophagus oesophagus
11 chr16:79882600-79883200 Bivalent Enhancer Fetal Muscle Trunk muscle
12 chr16:79882600-79883200 Enhancers Placenta Amnion Placenta Amnion
13 chr16:79882800-79883000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr16:79882800-79883200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr16:79882800-79883200 Enhancers Duodenum Mucosa Duodenum
16 chr16:79882800-79883600 Weak transcription Fetal Lung lung
17 chr16:79882800-79883600 Enhancers Placenta Placenta
18 chr16:79882800-79883600 Bivalent Enhancer Fetal Stomach stomach
19 chr16:79882800-79883800 Enhancers Fetal Intestine Large intestine
20 chr16:79882800-79883800 Enhancers Fetal Intestine Small intestine

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