Variant report

Variant rs182988
Chromosome Location chr5:112813566-112813567
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:112807800-112821600 Weak transcription HMEC breast
2 chr5:112810200-112823000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr5:112810400-112820600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr5:112810400-112821600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr5:112812800-112815800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr5:112813200-112813600 Enhancers Cortex derived primary cultured neurospheres brain
7 chr5:112813200-112814000 Enhancers Left Ventricle heart
8 chr5:112813200-112815000 Enhancers Fetal Heart heart
9 chr5:112813400-112813600 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr5:112813400-112814000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr5:112813400-112822800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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