Variant report

Variant rs544400022
Chromosome Location chr20:14965532-14965533
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:14963600-14965800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr20:14964600-14966800 Enhancers Fetal Intestine Large intestine
3 chr20:14964600-14971600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr20:14964800-14967800 Enhancers HUVEC blood vessel
5 chr20:14965000-14965600 Enhancers Stomach Mucosa stomach
6 chr20:14965000-14968000 Enhancers Liver Liver
7 chr20:14965200-14965600 Enhancers A549 lung
8 chr20:14965200-14965800 Flanking Active TSS HepG2 liver
9 chr20:14965200-14966000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr20:14965200-14967200 Enhancers Fetal Intestine Small intestine
11 chr20:14965400-14966000 Enhancers Duodenum Mucosa Duodenum
12 chr20:14965400-14966800 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr20:14965400-14967400 Enhancers Rectal Mucosa Donor 31 rectum
14 chr20:14965400-14967600 Enhancers Pancreas Pancrea
15 chr20:14965400-14968000 Enhancers Fetal Kidney kidney
16 chr20:14965400-14968000 Enhancers Hela-S3 cervix

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