Variant report

Variant rs385134
Chromosome Location chr6:145851005-145851006
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145850000-145851200 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
2 chr6:145850000-145851200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr6:145850000-145852600 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
4 chr6:145850400-145853200 Enhancers HUES64 Cell Line embryonic stem cell
5 chr6:145850400-145854200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
6 chr6:145850600-145851400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
7 chr6:145850600-145851800 Enhancers Pancreatic Islets Pancreatic Islet
8 chr6:145850600-145852000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr6:145850600-145852600 Enhancers HUES6 Cell Line embryonic stem cell
10 chr6:145850800-145851200 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
11 chr6:145850800-145851400 Enhancers Left Ventricle heart
12 chr6:145850800-145851400 Enhancers Pancreas Pancrea
13 chr6:145850800-145851600 Bivalent Enhancer H1 Cell Line embryonic stem cell
14 chr6:145850800-145851600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr6:145850800-145852200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr6:145850800-145854600 Bivalent Enhancer H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
17 chr6:145851000-145851600 Flanking Bivalent TSS/Enh iPS-20b Cell Line embryonic stem cell
18 chr6:145851000-145852400 Enhancers Stomach Mucosa stomach
19 chr6:145851000-145853200 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell

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