Variant report

Variant rs180848705
Chromosome Location chr4:100497148-100497149
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:100495600-100497200 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
2 chr4:100495600-100500400 Active TSS Fetal Intestine Large intestine
3 chr4:100495800-100500400 Active TSS Fetal Intestine Small intestine
4 chr4:100495800-100500800 Active TSS Duodenum Mucosa Duodenum
5 chr4:100496000-100497200 Active TSS Duodenum Smooth Muscle Duodenum
6 chr4:100496000-100497600 Active TSS HepG2 liver
7 chr4:100496200-100497200 Active TSS H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr4:100496200-100498200 Active TSS Liver Liver
9 chr4:100496400-100497200 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr4:100496400-100497200 Active TSS Stomach Smooth Muscle stomach
11 chr4:100496800-100497200 Flanking Active TSS Cortex derived primary cultured neurospheres brain
12 chr4:100497000-100497200 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain

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