Variant report

Variant rs1998155
Chromosome Location chr20:24757964-24757965
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:24749200-24763600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr20:24751000-24761200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr20:24753400-24761200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr20:24754400-24758600 Weak transcription Fetal Muscle Leg muscle
5 chr20:24755000-24758800 Weak transcription Thymus Thymus
6 chr20:24755600-24758600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr20:24755800-24758400 Weak transcription A549 lung
8 chr20:24757600-24758200 Enhancers Pancreas Pancrea
9 chr20:24757600-24758600 Weak transcription Esophagus oesophagus
10 chr20:24757600-24759400 Weak transcription HMEC breast
11 chr20:24757800-24758000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr20:24757800-24758200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr20:24757800-24766600 Enhancers Fetal Thymus thymus

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