Variant report

Variant rs11119380
Chromosome Location chr1:210157554-210157555
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210146600-210160400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:210153200-210158800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr1:210156200-210159000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:210157000-210157800 Enhancers Brain Cingulate Gyrus brain
5 chr1:210157200-210157600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr1:210157200-210157600 Genic enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:210157200-210157600 Enhancers Brain Hippocampus Middle brain
8 chr1:210157200-210157800 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr1:210157200-210157800 Enhancers Fetal Brain Female brain
10 chr1:210157400-210157600 Enhancers H9 Cell Line embryonic stem cell
11 chr1:210157400-210157600 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr1:210157400-210157600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
13 chr1:210157400-210157800 Enhancers Brain Dorsolateral Prefrontal Cortex brain

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