Variant report

Variant rs61989239
Chromosome Location chr14:71705928-71705929
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:71695800-71709400 Weak transcription Pancreas Pancrea
2 chr14:71699600-71707400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr14:71702800-71706800 Weak transcription Spleen Spleen
4 chr14:71703000-71706800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr14:71703000-71706800 Weak transcription Esophagus oesophagus
6 chr14:71703000-71707200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr14:71703000-71709000 Weak transcription Right Atrium heart
8 chr14:71703200-71708600 Weak transcription Brain Cingulate Gyrus brain
9 chr14:71703400-71706800 Weak transcription Fetal Lung lung
10 chr14:71703400-71708400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr14:71703400-71709000 Weak transcription Brain Inferior Temporal Lobe brain
12 chr14:71703600-71706800 Weak transcription Fetal Muscle Leg muscle
13 chr14:71703600-71707200 Weak transcription NHEK skin
14 chr14:71703600-71707400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr14:71704600-71707600 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr14:71704600-71713200 Weak transcription Thymus Thymus
17 chr14:71705800-71708200 Weak transcription Stomach Smooth Muscle stomach
18 chr14:71705800-71708200 Weak transcription NHDF-Ad bronchial

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