Variant report

Variant rs6435669
Chromosome Location chr2:212631614-212631615
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:212621200-212632800 Weak transcription Aorta Aorta
2 chr2:212630600-212631800 Enhancers Dnd41 blood
3 chr2:212630800-212631800 Enhancers Brain Cingulate Gyrus brain
4 chr2:212631000-212631800 Enhancers Brain Hippocampus Middle brain
5 chr2:212631000-212632000 Enhancers HUES48 Cell Line embryonic stem cell
6 chr2:212631000-212632000 Enhancers Placenta Placenta
7 chr2:212631200-212632000 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr2:212631200-212632000 Active TSS Rectal Mucosa Donor 29 rectum
9 chr2:212631200-212633200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr2:212631400-212631800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr2:212631400-212631800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr2:212631400-212631800 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
13 chr2:212631400-212631800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr2:212631400-212631800 Enhancers HMEC breast
15 chr2:212631600-212631800 Enhancers Sigmoid Colon Sigmoid Colon

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