Variant report

Variant rs12077089
Chromosome Location chr1:85298014-85298015
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85289400-85330800 Weak transcription iPS-20b Cell Line embryonic stem cell
2 chr1:85291000-85300000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr1:85291200-85301000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:85294400-85299400 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr1:85294600-85299200 Weak transcription HMEC breast
6 chr1:85294600-85300400 Weak transcription Fetal Heart heart
7 chr1:85296000-85300200 Weak transcription NHLF lung
8 chr1:85296400-85299200 Weak transcription Pancreas Pancrea
9 chr1:85296600-85299200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:85296600-85312800 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr1:85296800-85299000 Weak transcription NHEK skin
12 chr1:85297000-85299400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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