Variant report

Variant rs551815996
Chromosome Location chr1:85294292-85294293
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85264000-85295600 Weak transcription NHEK skin
2 chr1:85282400-85295800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:85287600-85295800 Weak transcription Right Atrium heart
4 chr1:85288800-85296800 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr1:85289400-85330800 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr1:85291000-85296000 Weak transcription Right Ventricle heart
7 chr1:85291000-85300000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:85291200-85301000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr1:85291600-85296000 Weak transcription Left Ventricle heart
10 chr1:85292600-85294600 Enhancers Fetal Heart heart
11 chr1:85293800-85294400 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr1:85294200-85294600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:85294200-85294600 Enhancers HMEC breast

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