Variant report

Variant rs577682820
Chromosome Location chr17:37753614-37753615
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:37748800-37754400 Weak transcription Pancreas Pancrea
2 chr17:37751200-37756000 Bivalent Enhancer Fetal Brain Male brain
3 chr17:37751400-37755000 Bivalent Enhancer Brain Germinal Matrix brain
4 chr17:37752400-37754800 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
5 chr17:37752800-37754400 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr17:37752800-37755600 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
7 chr17:37752800-37756400 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
8 chr17:37752800-37756800 Bivalent Enhancer Primary T cells fromperipheralblood blood
9 chr17:37752800-37757800 Bivalent Enhancer Fetal Muscle Leg muscle
10 chr17:37752800-37760200 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
11 chr17:37753200-37756400 Bivalent Enhancer Left Ventricle heart
12 chr17:37753400-37754200 Bivalent Enhancer Fetal Heart heart
13 chr17:37753400-37755000 Bivalent Enhancer Ganglion Eminence derived primary cultured neurospheres brain
14 chr17:37753400-37755800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
15 chr17:37753400-37756400 Bivalent Enhancer Primary T killer naive cells fromperipheralblood blood
16 chr17:37753600-37754000 Active TSS Fetal Brain Female brain

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