Variant report

Variant rs2001097
Chromosome Location chr6:32383858-32383859
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:32368400-32385600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:32383400-32384000 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
3 chr6:32383400-32384000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr6:32383400-32384000 Flanking Bivalent TSS/Enh HUVEC blood vessel
5 chr6:32383600-32384000 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr6:32383800-32384000 Enhancers H1 Cell Line embryonic stem cell
7 chr6:32383800-32384000 Enhancers HUES48 Cell Line embryonic stem cell
8 chr6:32383800-32384000 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
9 chr6:32383800-32384000 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr6:32383800-32384000 Bivalent Enhancer Monocytes-CD14+_RO01746 blood
11 chr6:32383800-32384000 Enhancers NH-A brain
12 chr6:32383800-32384000 Bivalent Enhancer NHEK skin

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