Variant report

Variant rs35311789
Chromosome Location chr14:104655234-104655235
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104643800-104662200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr14:104652400-104655800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr14:104652600-104660400 Weak transcription Spleen Spleen
4 chr14:104653400-104655400 Bivalent Enhancer Placenta Placenta
5 chr14:104653600-104656200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr14:104653800-104655400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
7 chr14:104654400-104655400 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr14:104654400-104655400 Enhancers Rectal Mucosa Donor 31 rectum
9 chr14:104654600-104655600 Bivalent Enhancer Stomach Mucosa stomach
10 chr14:104655000-104655400 Active TSS H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr14:104655000-104655400 Enhancers Gastric stomach
12 chr14:104655000-104661400 Weak transcription Fetal Brain Male brain

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