Variant report

Variant rs4507559
Chromosome Location chr6:167821064-167821065
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167817800-167821200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr6:167820200-167821400 Enhancers HUES48 Cell Line embryonic stem cell
3 chr6:167820200-167821600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr6:167820400-167821600 Enhancers HUES6 Cell Line embryonic stem cell
5 chr6:167820400-167822200 Enhancers H1 Cell Line embryonic stem cell
6 chr6:167820800-167821400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
7 chr6:167820800-167821400 Flanking Bivalent TSS/Enh HepG2 liver
8 chr6:167820800-167822200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr6:167821000-167821400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr6:167821000-167821400 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr6:167821000-167821400 Enhancers Pancreas Pancrea
12 chr6:167821000-167821600 Enhancers Cortex derived primary cultured neurospheres brain
13 chr6:167821000-167821600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
14 chr6:167821000-167822200 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast

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