Variant report

Variant rs552771998
Chromosome Location chr14:104789472-104789473
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104786800-104793200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr14:104788400-104792000 Weak transcription Spleen Spleen
3 chr14:104788600-104790000 Enhancers Brain Germinal Matrix brain
4 chr14:104788800-104789600 Bivalent Enhancer Fetal Stomach stomach
5 chr14:104788800-104789600 Bivalent Enhancer Rectal Mucosa Donor 29 rectum
6 chr14:104789200-104790200 Enhancers Fetal Brain Male brain
7 chr14:104789200-104790800 Enhancers Rectal Mucosa Donor 31 rectum
8 chr14:104789400-104789600 Bivalent Enhancer Colonic Mucosa Colon
9 chr14:104789400-104789600 Enhancers Fetal Intestine Small intestine
10 chr14:104789400-104789800 Weak transcription Sigmoid Colon Sigmoid Colon
11 chr14:104789400-104790200 Enhancers Duodenum Mucosa Duodenum
12 chr14:104789400-104790600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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