Variant report

Variant rs12716878
Chromosome Location chr16:79598840-79598841
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:79595000-79599000 Weak transcription Adipose Nuclei Adipose
2 chr16:79596000-79599000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
3 chr16:79596400-79599000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr16:79597800-79599400 Enhancers Fetal Intestine Large intestine
5 chr16:79597800-79599400 Enhancers Fetal Intestine Small intestine
6 chr16:79598200-79599000 Flanking Active TSS Liver Liver
7 chr16:79598400-79603200 Weak transcription iPS-20b Cell Line embryonic stem cell
8 chr16:79598600-79599000 Enhancers Duodenum Mucosa Duodenum
9 chr16:79598600-79603200 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr16:79598600-79603200 Weak transcription iPS-18 Cell Line embryonic stem cell
11 chr16:79598600-79604800 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr16:79598800-79599200 Bivalent Enhancer HepG2 liver
13 chr16:79598800-79605600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
14 chr16:79598800-79606400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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