Variant report

Variant rs56232771
Chromosome Location chr14:104839538-104839539
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104831000-104842000 Weak transcription Gastric stomach
2 chr14:104835400-104842000 Weak transcription Fetal Brain Male brain
3 chr14:104837600-104840200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr14:104838400-104839600 Enhancers Primary T helper naive cells fromperipheralblood blood
5 chr14:104838400-104839600 Enhancers Primary T helper cells fromperipheralblood blood
6 chr14:104838600-104839600 Enhancers Primary T cells fromperipheralblood blood
7 chr14:104838600-104839600 Enhancers Primary T helper memory cells from peripheral blood 2 blood
8 chr14:104838800-104839600 Enhancers Primary mononuclear cells fromperipheralblood Blood
9 chr14:104838800-104840000 Enhancers Primary T helper 17 cells PMA-I stimulated --
10 chr14:104838800-104840000 Enhancers Fetal Intestine Small intestine
11 chr14:104839000-104839600 Enhancers Fetal Intestine Large intestine
12 chr14:104839200-104840000 Enhancers Brain Germinal Matrix brain

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