Variant report

Variant rs1541910
Chromosome Location chr5:150962527-150962528
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:150959400-150965600 Weak transcription Pancreas Pancrea
2 chr5:150959600-150967400 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr5:150960000-150962600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr5:150960600-150965600 Weak transcription Adipose Nuclei Adipose
5 chr5:150961000-150962600 Flanking Active TSS NHEK skin
6 chr5:150961600-150962600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr5:150961600-150963800 Weak transcription Esophagus oesophagus
8 chr5:150961800-150968600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr5:150961800-150970400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
10 chr5:150962000-150962600 Enhancers Fetal Thymus thymus
11 chr5:150962000-150963800 Enhancers HMEC breast
12 chr5:150962000-150965400 Weak transcription Placenta Placenta
13 chr5:150962000-150965400 Weak transcription Skeletal Muscle Male skeletal muscle
14 chr5:150962000-150965400 Weak transcription Skeletal Muscle Female skeletal muscle
15 chr5:150962000-150965600 Weak transcription H1 Cell Line embryonic stem cell
16 chr5:150962000-150965600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr5:150962400-150962600 Transcr. at gene 5' and 3' Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr5:150962400-150962600 Enhancers Fetal Muscle Leg muscle

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