Variant report

Variant rs117715457
Chromosome Location chr21:47028093-47028094
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:47022000-47039000 Weak transcription Right Atrium heart
2 chr21:47026800-47028600 Enhancers Primary T helper memory cells from peripheral blood 2 blood
3 chr21:47026800-47028800 Enhancers Primary T helper cells PMA-I stimulated --
4 chr21:47026800-47029000 Enhancers Primary T helper naive cells fromperipheralblood blood
5 chr21:47026800-47029600 Enhancers Primary T cells fromperipheralblood blood
6 chr21:47027000-47028800 Enhancers Primary T helper cells fromperipheralblood blood
7 chr21:47027200-47028600 Enhancers Primary T helper naive cells from peripheral blood blood
8 chr21:47027200-47033400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr21:47027200-47037600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
10 chr21:47027600-47028600 Enhancers Primary T helper 17 cells PMA-I stimulated --
11 chr21:47027600-47028800 Enhancers Primary T helper memory cells from peripheral blood 1 blood
12 chr21:47027800-47028400 Bivalent Enhancer Fetal Muscle Leg muscle
13 chr21:47027800-47028600 Enhancers Primary T killer memory cells from peripheral blood blood
14 chr21:47028000-47028200 Flanking Bivalent TSS/Enh Foreskin Melanocyte Primary Cells skin01 Skin
15 chr21:47028000-47028600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin

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