Variant report

Variant rs12175049
Chromosome Location chr6:4295471-4295472
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:4288600-4295600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr6:4292200-4295600 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr6:4294200-4297000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
4 chr6:4294600-4296800 Enhancers Cortex derived primary cultured neurospheres brain
5 chr6:4295000-4295800 Enhancers Esophagus oesophagus
6 chr6:4295000-4296000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr6:4295000-4296600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr6:4295200-4296400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
9 chr6:4295200-4297200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr6:4295200-4298000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr6:4295400-4296000 Enhancers Brain Inferior Temporal Lobe brain
12 chr6:4295400-4296400 Enhancers Fetal Adrenal Gland Adrenal Gland

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