Variant report

Variant rs62181569
Chromosome Location chr2:181904158-181904159
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:181900600-181904400 Enhancers NHLF lung
2 chr2:181900800-181904200 Enhancers Osteobl bone
3 chr2:181901200-181904400 Enhancers NHDF-Ad bronchial
4 chr2:181901200-181912200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr2:181901400-181906400 Weak transcription Psoas Muscle Psoas
6 chr2:181901400-181910000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr2:181901600-181911200 Weak transcription GM12878-XiMat blood
8 chr2:181902200-181926400 Weak transcription HSMM muscle
9 chr2:181902600-181909800 Weak transcription Brain Germinal Matrix brain
10 chr2:181902800-181905600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr2:181902800-181934200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr2:181903000-181910200 Weak transcription Sigmoid Colon Sigmoid Colon
13 chr2:181903600-181905600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:181903600-181918800 Weak transcription NHEK skin
15 chr2:181903800-181904400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr2:181903800-181917000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
17 chr2:181903800-181934600 Weak transcription NH-A brain
18 chr2:181904000-181904400 Enhancers Left Ventricle heart

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