Variant report

Variant rs17437657
Chromosome Location chr7:27249617-27249618
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27245800-27253000 Weak transcription Gastric stomach
2 chr7:27249200-27250000 Bivalent Enhancer Fetal Intestine Large intestine
3 chr7:27249200-27250000 Bivalent Enhancer Fetal Intestine Small intestine
4 chr7:27249400-27251000 Flanking Bivalent TSS/Enh Rectal Mucosa Donor 29 rectum
5 chr7:27249400-27251000 Flanking Active TSS Rectal Mucosa Donor 31 rectum
6 chr7:27249600-27249800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
7 chr7:27249600-27249800 Bivalent Enhancer HepG2 liver
8 chr7:27249600-27250000 Enhancers A549 lung
9 chr7:27249600-27250600 Active TSS Rectal Smooth Muscle rectum
10 chr7:27249600-27251000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell

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