Variant report

Variant rs71369777
Chromosome Location chr17:37752205-37752206
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 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 chr17:37751400-37752600 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
4 chr17:37751400-37753200 Bivalent Enhancer H1 Cell Line embryonic stem cell
5 chr17:37751400-37755000 Bivalent Enhancer Brain Germinal Matrix brain
6 chr17:37751800-37752800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
7 chr17:37752000-37753000 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
8 chr17:37752200-37753200 Flanking Active TSS Fetal Brain Female brain
9 chr17:37752200-37753600 Bivalent Enhancer HSMMtube muscle

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