Variant report

Variant rs13050591
Chromosome Location chr21:45900796-45900797
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:45881800-45911800 Weak transcription Right Atrium heart
2 chr21:45896200-45905400 Weak transcription Brain Germinal Matrix brain
3 chr21:45898600-45905600 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr21:45898800-45902000 Weak transcription Fetal Intestine Small intestine
5 chr21:45898800-45902000 Weak transcription Placenta Placenta
6 chr21:45898800-45902400 Weak transcription Pancreas Pancrea
7 chr21:45898800-45905400 Weak transcription Fetal Brain Female brain
8 chr21:45898800-45906200 Weak transcription Spleen Spleen
9 chr21:45899000-45903800 Weak transcription Stomach Smooth Muscle stomach
10 chr21:45899800-45901000 Enhancers Liver Liver
11 chr21:45900000-45900800 Flanking Active TSS HepG2 liver
12 chr21:45900000-45901000 Flanking Active TSS Hela-S3 cervix
13 chr21:45900200-45900800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr21:45900200-45900800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr21:45900600-45900800 Enhancers H1 Cell Line embryonic stem cell
16 chr21:45900600-45900800 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
17 chr21:45900600-45901200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
18 chr21:45900600-45902000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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