Variant report

Variant rs566747799
Chromosome Location chr20:14687839-14687840
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14681600-14698200 Weak transcription Fetal Kidney kidney
2 chr20:14682000-14688800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr20:14682000-14689800 Weak transcription Rectal Mucosa Donor 29 rectum
4 chr20:14682200-14692200 Weak transcription Fetal Heart heart
5 chr20:14682200-14693000 Weak transcription Sigmoid Colon Sigmoid Colon
6 chr20:14685600-14688800 Weak transcription NHEK skin
7 chr20:14686000-14688600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr20:14686200-14694600 Weak transcription H9 Cell Line embryonic stem cell
9 chr20:14687200-14688000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr20:14687200-14688000 Flanking Active TSS Liver Liver
11 chr20:14687200-14689000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr20:14687200-14692800 Weak transcription Ovary ovary
13 chr20:14687400-14688000 Enhancers ES-I3 Cell Line embryonic stem cell
14 chr20:14687400-14689200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr20:14687600-14688600 Enhancers HUES64 Cell Line embryonic stem cell
16 chr20:14687600-14688800 Enhancers iPS-20b Cell Line embryonic stem cell
17 chr20:14687600-14689200 Enhancers Fetal Lung lung
18 chr20:14687600-14692000 Weak transcription Placenta Amnion Placenta Amnion
19 chr20:14687800-14688200 Enhancers iPS-15b Cell Line embryonic stem cell

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