Variant report

Variant rs3764406
Chromosome Location chr17:18282676-18282677
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:18267200-18288200 Weak transcription Right Atrium heart
2 chr17:18280400-18284200 Enhancers Stomach Mucosa stomach
3 chr17:18280600-18283200 Enhancers Placenta Amnion Placenta Amnion
4 chr17:18280600-18283800 Enhancers Placenta Placenta
5 chr17:18281400-18283000 Weak transcription Fetal Thymus thymus
6 chr17:18281400-18286400 Weak transcription Gastric stomach
7 chr17:18281600-18283600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr17:18281600-18283800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr17:18281800-18282800 Active TSS Hela-S3 cervix
10 chr17:18281800-18283400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr17:18281800-18283600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr17:18282400-18283200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr17:18282600-18282800 Bivalent Enhancer Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr17:18282600-18282800 Enhancers Duodenum Mucosa Duodenum
15 chr17:18282600-18282800 Enhancers Rectal Mucosa Donor 29 rectum
16 chr17:18282600-18282800 Enhancers HMEC breast
17 chr17:18282600-18283000 Enhancers Colonic Mucosa Colon
18 chr17:18282600-18283000 Enhancers NHEK skin
19 chr17:18282600-18283800 Enhancers Esophagus oesophagus

Quick Search:


  
Input of quick search could be:

what's new

Quick links