Variant report

Variant rs552952713
Chromosome Location chr5:150942050-150942051
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:150908200-150948000 Strong transcription HMEC breast
2 chr5:150908400-150944000 Strong transcription NHEK skin
3 chr5:150909200-150942400 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr5:150911600-150942800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr5:150918200-150945400 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr5:150931000-150942800 Weak transcription Brain Angular Gyrus brain
7 chr5:150934200-150949600 Weak transcription Skeletal Muscle Male skeletal muscle
8 chr5:150937000-150948600 Weak transcription Right Atrium heart
9 chr5:150937600-150948600 Weak transcription Adipose Nuclei Adipose
10 chr5:150940800-150942600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr5:150940800-150943200 Genic enhancers Breast Myoepithelial Primary Cells Breast
12 chr5:150941400-150942200 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr5:150941400-150942600 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr5:150941600-150942200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr5:150941800-150942200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr5:150941800-150942200 Genic enhancers Esophagus oesophagus

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