Variant report

Variant rs4712224
Chromosome Location chr6:14060276-14060277
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:14057200-14060400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr6:14058800-14060400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr6:14058800-14060400 Weak transcription NH-A brain
4 chr6:14059800-14061400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:14059800-14061600 Enhancers Hela-S3 cervix
6 chr6:14060000-14060600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr6:14060000-14060600 Bivalent Enhancer Brain Hippocampus Middle brain
8 chr6:14060000-14060600 Enhancers Esophagus oesophagus
9 chr6:14060000-14060600 Bivalent Enhancer Left Ventricle heart
10 chr6:14060000-14060600 Enhancers NHDF-Ad bronchial
11 chr6:14060000-14060600 Flanking Active TSS NHEK skin
12 chr6:14060000-14061400 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr6:14060000-14061600 Enhancers Cortex derived primary cultured neurospheres brain
14 chr6:14060200-14060400 Bivalent Enhancer Brain Substantia Nigra brain
15 chr6:14060200-14060400 Flanking Bivalent TSS/Enh HSMMtube muscle
16 chr6:14060200-14060600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr6:14060200-14060600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr6:14060200-14060600 Enhancers Lung lung
19 chr6:14060200-14060600 Flanking Active TSS HMEC breast
20 chr6:14060200-14061000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
21 chr6:14060200-14061400 Enhancers Liver Liver

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