Variant report

Variant rs9392311
Chromosome Location chr6:1627547-1627548
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:1616800-1631400 Weak transcription Hela-S3 cervix
2 chr6:1622600-1629000 Active TSS Aorta Aorta
3 chr6:1625200-1634000 Weak transcription Gastric stomach
4 chr6:1625800-1628000 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr6:1625800-1639400 Weak transcription Ovary ovary
6 chr6:1626200-1627800 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
7 chr6:1626200-1636800 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr6:1626400-1627600 Bivalent Enhancer HUVEC blood vessel
9 chr6:1626400-1628800 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr6:1626400-1633600 Weak transcription Colonic Mucosa Colon
11 chr6:1626400-1637000 Weak transcription Pancreas Pancrea
12 chr6:1626600-1629800 Weak transcription HepG2 liver
13 chr6:1626800-1628600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr6:1627000-1628400 Bivalent Enhancer Fetal Kidney kidney
15 chr6:1627000-1628600 Enhancers Osteobl bone
16 chr6:1627000-1628800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr6:1627400-1627600 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
18 chr6:1627400-1627800 Bivalent Enhancer HUES6 Cell Line embryonic stem cell

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