Variant report

Variant rs6745453
Chromosome Location chr2:38623850-38623851
allele A/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:38605200-38624400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:38612200-38633200 Weak transcription Stomach Smooth Muscle stomach
3 chr2:38620200-38625800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr2:38620600-38624200 Enhancers HMEC breast
5 chr2:38621200-38624600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr2:38622200-38626600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:38622600-38624000 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr2:38622800-38624000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:38623000-38624800 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr2:38623800-38625200 Weak transcription NHEK skin

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