Variant report

Variant rs11934393
Chromosome Location chr4:119316366-119316367
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:119311200-119318200 Weak transcription NHDF-Ad bronchial
2 chr4:119315200-119316800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr4:119315400-119316800 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr4:119315400-119317200 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr4:119315400-119317400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr4:119315800-119317000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr4:119316000-119316800 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
8 chr4:119316000-119318000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr4:119316200-119320000 Enhancers HUES64 Cell Line embryonic stem cell
10 chr4:119316200-119320800 Enhancers ES-I3 Cell Line embryonic stem cell

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