Variant report

Variant rs117869237
Chromosome Location chr20:14965392-14965393
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14960600-14965400 Weak transcription Rectal Mucosa Donor 31 rectum
2 chr20:14960800-14965400 Weak transcription Hela-S3 cervix
3 chr20:14963600-14965800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr20:14964600-14966800 Enhancers Fetal Intestine Large intestine
5 chr20:14964600-14971600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr20:14964800-14967800 Enhancers HUVEC blood vessel
7 chr20:14965000-14965600 Enhancers Stomach Mucosa stomach
8 chr20:14965000-14968000 Enhancers Liver Liver
9 chr20:14965200-14965600 Enhancers A549 lung
10 chr20:14965200-14965800 Flanking Active TSS HepG2 liver
11 chr20:14965200-14966000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr20:14965200-14967200 Enhancers Fetal Intestine Small intestine

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