Variant report

Variant rs6942045
Chromosome Location chr6:33351696-33351697
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:33341000-33352400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:33341200-33358600 Weak transcription H9 Cell Line embryonic stem cell
3 chr6:33343800-33359200 Weak transcription Right Atrium heart
4 chr6:33344000-33351800 Weak transcription Esophagus oesophagus
5 chr6:33345600-33358800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr6:33348400-33358800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr6:33348600-33352600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr6:33350200-33351800 Enhancers Stomach Smooth Muscle stomach
9 chr6:33350200-33352400 Weak transcription K562 blood
10 chr6:33350200-33352600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr6:33351200-33351800 Enhancers HepG2 liver
12 chr6:33351600-33351800 Flanking Active TSS H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr6:33351600-33351800 Enhancers Colon Smooth Muscle Colon
14 chr6:33351600-33352000 Enhancers Fetal Intestine Small intestine

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