Variant report

Variant rs12999247
Chromosome Location chr2:187346255-187346256
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187320600-187347400 Weak transcription Rectal Mucosa Donor 31 rectum
2 chr2:187328000-187350400 Weak transcription Pancreas Pancrea
3 chr2:187337000-187347000 Weak transcription HepG2 liver
4 chr2:187337000-187348000 Weak transcription Duodenum Mucosa Duodenum
5 chr2:187339800-187347400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr2:187339800-187348400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:187339800-187349800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr2:187344000-187348000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr2:187345000-187347400 Enhancers NHEK skin
10 chr2:187345400-187346400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr2:187345800-187346400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr2:187345800-187346400 Enhancers Fetal Intestine Small intestine
13 chr2:187345800-187346600 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr2:187346200-187346400 Enhancers HMEC breast
15 chr2:187346200-187346600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr2:187346200-187348200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

Quick Search:


  
Input of quick search could be:

what's new

Quick links